U.S. patent application number 11/909276 was filed with the patent office on 2009-09-03 for methods for the treatment of a traumatic central nervous system injury via a tapered administration protocol.
This patent application is currently assigned to Emory University. Invention is credited to Sarah Cutler, Donald G. Stein.
Application Number | 20090221544 11/909276 |
Document ID | / |
Family ID | 36987966 |
Filed Date | 2009-09-03 |
United States Patent
Application |
20090221544 |
Kind Code |
A1 |
Stein; Donald G. ; et
al. |
September 3, 2009 |
METHODS FOR THE TREATMENT OF A TRAUMATIC CENTRAL NERVOUS SYSTEM
INJURY VIA A TAPERED ADMINISTRATION PROTOCOL
Abstract
The present invention provides methods for the treatment or the
prevention of neuronal damage in the CNS. Specifically, the methods
of the invention provide for the administration of a
therapeutically effective amount of a progestin or progestin
metabolite following a traumatic or ischemic injury to the CNS such
that, prior to termination of administration of the progestin or
progestin metabolite the administration is tapered to avoid
withdrawal. The drug taper employed can involve a linear taper, an
exponential taper, progressively dividing administered doses by
50%, or can be determined based on the treating physician's
assessment of the patient's response to therapy. The tapered
administration methods of the present invention may be used in
combination with any therapeutic protocol or regimen for the
administration of a therapeutically effective amount of a progestin
or progestin metabolite to treat a traumatic or ischemic CNS
injury.
Inventors: |
Stein; Donald G.; (Atlanta,
GA) ; Cutler; Sarah; (Atlanta, GA) |
Correspondence
Address: |
FOLEY AND LARDNER LLP;SUITE 500
3000 K STREET NW
WASHINGTON
DC
20007
US
|
Assignee: |
Emory University
Atlanta
GA
|
Family ID: |
36987966 |
Appl. No.: |
11/909276 |
Filed: |
March 24, 2006 |
PCT Filed: |
March 24, 2006 |
PCT NO: |
PCT/US06/10984 |
371 Date: |
May 13, 2009 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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60664728 |
Mar 24, 2005 |
|
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60729663 |
Oct 24, 2005 |
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Current U.S.
Class: |
514/177 |
Current CPC
Class: |
A61P 25/00 20180101;
A61P 25/28 20180101; A61P 9/00 20180101; A61K 31/57 20130101 |
Class at
Publication: |
514/177 |
International
Class: |
A61K 31/57 20060101
A61K031/57 |
Goverment Interests
FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0001] This invention was made with United States Government
support under grant numbers R01 N5038664-04 and R01N5040825-03
awarded by the National Institute of Neurological Disorders and
Stroke (NINDS) of the National Institutes of Health. The United
States Government has certain rights in the invention.
Claims
1. A method of treating a traumatic central nervous system injury,
said method comprising administering a therapeutically effective
amount of progesterone to a subject in need thereof, wherein prior
to termination of administration of progesterone said
administration comprises a tapered administration dosing
regimen.
2. The method of claim 1, wherein said traumatic central nervous
system injury is a traumatic brain injury.
3. The method of claim 2, wherein said traumatic brain injury
results from a blunt force contusion.
4. The method of claim 1, wherein said tapered administration
dosing regimen comprises progressively dividing administered doses
of progesterone by 50%.
5. The method of claim 1, wherein said tapered administration
dosing regimen comprises a linear taper.
6. The method of claim 5, wherein said linear taper is a 10% linear
taper.
7. The method of claim 1, wherein said tapered administration
dosing regimen comprises an exponential taper.
8. The method of claim 1, wherein said tapered administration
dosing regimen is used in combination with administration of
progesterone at least once a day.
9. The method of claim 1, wherein said therapeutically effective
amount of progesterone administered to said subject prior to the
tapered administration dosing regime comprises a constant
progesterone dosing regimen.
10. The method of claim 1, wherein said therapeutically effective
amount of progesterone administered to said subject prior to the
tapered administration dosing regime comprises a two-level
progesterone dosing regimen.
Description
FIELD OF THE INVENTION
[0002] The invention relates to methods for treating a traumatic or
ischemic injury to the central nervous system.
BACKGROUND OF THE INVENTION
[0003] There is growing experimental evidence that progesterone,
its metabolites and other gonadal steroids such as estrogen and
possibly testosterone, are effective neuroprotective agents;
although the specific, physiological mechanisms by which these
hormones act in the central nervous system to enhance repair are
not completely understood. In addition to being a gonadal steroid,
progesterone also belongs to a family of autocrine/paracrine
hormones called neurosteroids. Neurosteroids are steroids that
accumulate in the brain independently of endocrine sources and
which can be synthesized from sterol precursors in glial cells.
These neurosteroids can potentiate GABA transmission, modulate the
effects of glutamate, enhance the production of myelin, reduce the
expression of inflammatory cytokines and prevent release of free
radicals from activated microglia.
[0004] In vivo data has demonstrated progesterone's neuroprotective
effects in injured nervous systems. For example, following a
contusion injury, progesterone reduces the severity of post injury
cerebral edema. The attenuation of edema by progesterone is
accompanied by the sparing of neurons from secondary neuronal death
and improvements in cognitive outcome (Roof et al. (1994)
Experimental Neurology 129:64-69). Furthermore, following ischemic
injury in rats, progesterone has been shown to reduce cell damage
and neurological deficit (Jiang et al. (1996) Brain Research
735:101-107). Progesterone's protective effects may be mediated
thorough its interaction with GABA and/or glutamate receptors as
well as its effects on inflammatory cytokines and aquaporin
expression which are mediated by the intranuclear progesterone
receptor.
[0005] Various metabolites of progesterone have also been suggested
to have neuroprotective properties. For instance, the progesterone
metabolites allopregnanolone or epipregnanolone are positive
modulators of the GABA receptor, increasing the effects of GABA in
a manner that is independent of the benzodiazepines (Baulieu, E. E.
(1992) Adv. Biochem. Psychopharmacol. 47:1-16; Robel et al. (1995)
Crit. Rev. Neurobiol. 9:383-94; Lambert et al. (1995) Trends
Pharmacol. Sci. 16:295-303; Baulieu, E. E. (1997) Recent Prog.
Horm. Res. 52:1-32; Reddy et al. (1996) Psychopharmacology
128:280-92). In addition, these neurosteroids act as antagonists at
the sigma receptor: a receptor that can activate the NMDA channel
complex (Maurice et al. (1998) Neuroscience 83:413-28; Maurice et
al. (1996) J. Neurosci. Res. 46:734-43; Reddy et al. (1998)
Neuroreport 9:3069-73). These neurosteroids have also been shown to
reduce the stimulation of cholinergic neurons and the subsequent
release of acetylcholine by excitability. Numerous studies have
shown that the cholinergic neurons of the basal forebrain are
sensitive to traumatic brain injury and that excessive release of
acetylcholine can be more excitotoxic than glutamate (Lyeth et al.
(1992) J. Neurotrauma 9(2):S463-74; Hayes et al. (1992) J.
Neurotrauma 9(1):S173-87).
[0006] Following a traumatic injury to the central nervous system,
a cascade of physiological events leads to neuronal loss including,
for example, an inflammatory immune response and excitotoxicity
resulting from the initial impact disrupting the glutamate,
acetylcholine, cholinergic, GABA.sub.A, and NMDA receptor systems.
In addition, the traumatic CNS injury is frequently followed by
brain and/or spinal cord edema that enhances the cascade of injury
and leads to further secondary cell death and increased patient
mortality.
[0007] Other kinds of CNS injury can set into motion different
physiological events that lead to neuronal loss. For example,
ischemic injury occurs when blood flow to the CNS is interrupted.
During ischemia, consumed cellular ATP usually cannot be adequately
replenished in the absence of a supply of oxygen. Other
physiological events associated with ischemic CNS injury include
release or overexpression of proteins such as neuron-specific
enolase (NSE), myelin basic protein, glial fibrillary acidic
protein (GFAP), the S-100 protein, and the gamma isoform of protein
kinase C (PKCg), stimulation of membrane phospholipid degradation
and subsequent free-fatty-acid accumulation, cellular acidosis,
glutamate release and excitotoxicity, calcium ion influx, and free
radical generation.
[0008] Significant ischemia in the CNS occurs with stroke, leading
to rapid cell death in the core regions of the stroke where blood
flow is reduced to about 20% of normal levels. However, there is a
larger area of potential injury, called the ischemic penumbra,
where blood flow is reduced to a lesser extent. Cells in this
region are endangered, but may not be irreversibly damaged.
[0009] Because of limitations in current therapies for CNS injuries
as described above, improved methods for treating traumatic and
ischemic CNS injury are needed.
SUMMARY OF THE INVENTION
[0010] Methods for the treatment or the prevention of neuronal
damage in the CNS are provided. In particular, the present
invention provides a method of administration of a therapeutically
effective amount of a progestin or progestin metabolite following a
traumatic or ischemic injury to the CNS such that, prior to
termination of the progestin or progestin metabolite administration
is tapered to avoid withdrawal. The drug taper employed can involve
a linear taper, an exponential taper, progressively dividing
administered doses by 50%, or can be determined based on the
treating physician's assessment of the patient's response to
therapy. The tapered administration methods of the present
invention may be used in combination with any therapeutic protocol
or regimen for the administration of a therapeutically effective
amount of a progestin or progestin metabolite to treat a traumatic
or ischemic CNS injury.
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] FIG. 1 shows a dosage response curve for behavioral recovery
following a traumatic brain injury. FIGS. 1A and 113 demonstrate
that following treatment with low (8 mg/kg), moderate (16 mg/kg),
and high (32 mg/kg) doses of progesterone in a
cyclodextrin-containing carrier, both low and moderate doses of
progesterone produced consistent improvement in Morris water maze
performance.
[0012] FIG. 2 shows the results from the "sticker removal task"
following treatment with low (8 mg/kg), moderate (16 mg/kg), and
high (32 mg/kg) dosages of progesterone in a
cyclodextrin-containing carrier.
[0013] FIG. 3 shows somatosensory neglect data at one day (FIG. 3A)
and one week (FIG. 3B) post-withdrawal. FIG. 3A shows that at one
day post-withdrawal, TWL animals showed decreased latency compared
to VL and AWL animals (#, p<0.05). AWS rats demonstrated
elevated sensory deficiencies compared to the TWS and VS groups (*,
p<0.05). FIG. 3B shows that at one week post-withdrawal, sham
animals demonstrated equivalent latency, while tapered treatment
maintained decreased latency compared to acute and vehicle
treatment (#, p<0.05).
[0014] FIG. 4 shows center time, as determined from Digiscan
Locomoter Activity Boxes, between one FIG. 4A) and seven (FIG. 4B)
days post-withdrawal. FIG. 4A shows that one day after withdrawal,
center time was increased for TWS animals compared to all other
shams (#, p<0.05), while TWL center time was increased compared
to other lesion groups (**, p<0.05). AWL animals increased
center time compared to vehicle animals (##, p<0.05), and AWS
animals significantly decreased center time compared to VS animals
(*, p<0.05). FIG. 4B showed that TWL center time one week after
withdrawal is increased over AWL (**, p<0.05), which is
increased over VL (##, p<0.05). No difference was seen between
sham groups.
[0015] FIG. 5 shows p53 Western blotting densitometry between
experimental groups demonstrating an increase in apoptotic activity
for VL animals over all other treatment groups (*, p<0.05).
[0016] FIG. 6 shows HSP70 Western blotting densitometry between
experimental groups demonstrating an increase for TWL animals over
all other groups (*, p<0.05).
[0017] FIG. 7 shows BDNF Western blot densitometry between
experimental groups demonstrating an increase for TWL animals over
all other groups (*, p<0.05), followed by AWL (#, p<0.05). VL
BDNF levels were comparable to shams.
[0018] FIG. 8 shows representative images of selected sections
anterior to bregma (FIG. 8A), and quantified data for each lesion
group (FIG. 8B). FIG. 8A shows representative thionin-stained
sections at mm anterior to bregma for lesion animals. FIG. 8B shows
percent lesion volume at 3 weeks post-injury is greatest in
vehicle-treated animals, followed by those with acute withdrawal
(*, p<0.05) and tapered withdrawal (#, p<0.05).
[0019] FIG. 9 shows relative reactive astrocytes as determined by
immunofluorescent GFAP staining at three weeks post-injury. FIG. 9A
shows immunofluorescent staining for GFAP in brain slices from the
following groups: (A) VL; (B) AWL; (C) TWL; (D) VS; (E) AWS; and
(F) TWS. Images are shown at 40.times., with 10 .mu.m represented.
FIG. 9B shows quantification of luminosity for GFAP
immunofluorescent staining of reactive astrocytes indicates the
greatest response in VL (*, p<0.05) animals, followed by AWL
(**, p<0.05) and TWL animals. AWS animals had significantly
elevated levels of reactive astrocytes compared to other sham
groups m (#, p<0.05).
DETAILED DESCRIPTION OF THE INVENTION
[0020] The present invention provides methods and compositions for
the treatment or prevention of neurodegeneration following a
traumatic or ischemic injury to the central nervous system. In
particular, the methods of the invention provide for the
administration of a therapeutically effective amount of a progestin
or progestin metabolite following a traumatic or ischemic injury to
the CNS such that, prior to termination of administration of the
progestin or progestin metabolite the administration is tapered to
avoid withdrawal. As described in further detail elsewhere herein,
the present invention demonstrates that the tapered administration
allows for a more beneficial CNS repair than when an abrupt
termination of the progestin or progestin metabolite occurs.
[0021] By "treatment" is intended any improvement in the subject
having the traumatic or ischemic injury including both improved
morphological (i.e., enhanced tissue viability) and/or behavioral
recovery. The improvement can be characterized as an increase in
either the rate and/or the extent of behavioral and anatomical
recovery following the traumatic or ischemic CNS injury.
Accordingly, a "positive therapeutic response" induces both a
complete response and a partial response. Various methods to
determine if a complete or partial therapeutic response has
occurred are disclosed elsewhere herein.
[0022] Neurodegeneration is the progressive loss of neurons in the
central nervous system. As used herein, "neuroprotection" is the
arrest and/or reverse progression of neurodegeneration following a
traumatic or ischemic central nervous system injury. Hence, the
methods of the invention also find use in reducing and/or
preventing the physiological events leading to neurodegeneration.
Specifically, the present invention provides methods for reducing
or eliminating neuronal cell death, edema, ischemia, and enhancing
tissue viability following a traumatic or ischemic injury to the
central nervous system.
[0023] The sex hormones are steroids that may be classified into
functional groups according to chemical structure and physiological
activity and include estrogenic hormones, progestational hormones,
and androgenic hormones. Of particular interest in the methods of
the present invention are progestational hormones, referred to
herein as "progestins" or "progestogens", and their derivatives and
bioactive metabolites. Members of this broad family include steroid
hormones disclosed in Remington's Pharmaceutical Sciences, Gennaro
et al., Mack Publishing Co. (18.sup.th ed. 1990), 990-993. As with
all other classes of steroids, sterioisomerism is of fundamental
importance with the sex hormones. Hence, a variety of progestins
(i.e., progesterone) and their derivatives are encompassed by the
present invention, including both synthetic and natural products.
In one aspect of the invention, the progestin or progestin
metabolite is progesterone.
[0024] The term "progesterone" as used herein refers to a member of
the progestin family and comprises a 21 carbon steroid hormone.
Progesterone is also known as D4-pregnene-3,20-dione;
.delta.4-pregnene-3,20-dione; or pregn-4-ene-3,20-dione and it its
structure is provided below as formula (I). The progesterone used
in the methods of the invention can be naturally occurring or
synthetic.
##STR00001##
[0025] Further encompassed by the methods of the invention are
synthetic progestins. As used herein a "synthetic progestin" is a
molecule whose structure is related to that of progesterone, is
synthetically derived, and retains the biologically activity of
progesterone (i.e., treats a traumatic CNS injury). Representative
synthetic progestin include, but are not limited to, modifications
that produce 17a-OH esters (i.e., 17.alpha.-hydroxyprogesterone
caproate), as well as, modifications that introduce
6.alpha.-methyl, 6-Me, 6-ene, and 6-chloro substituents onto
progesterone (i.e., medroxyprogesterone acetate, megestrol acetate,
and chlomadinone acetate). Table 1 provides further, non-limiting
examples, of synthetic progestins.
TABLE-US-00001 TABLE 1 Classification of Synthetic Progestins
Classification Usual classification by generation* by structure
First Second Third Estranes Ethynodiol diacetate (with -- --
ethinyl estradiol: Demulen) Norethindrone (Micronor) Norethindrone
acetate (Aygestin) Gonanes Norgestrel (Ovrette) Levonorgestrel
Desogestrel (with ethinyl (Norplant; with estradiol: Desogen)
Gestodene.dagger. ethinyl estradiol: Norgestimate (with ethinyl
Alesse, Nordette) estradiol: Ortho-Cyclen, Ortho Tri-Cyclen)
Pregnanes Medroxyprogesterone -- -- acetate (Provera) * -- The
traditional classification is based on time since market
introduction and not on structural and physiologic differences or
efficacy.
[0026] As used herein, by "bioactive metabolite" or "derivative" of
progestin is intended any naturally or synthetically produced
progestin that prevents or retards neurodegeneration. Such
progestin derivatives include, for example, derivatives of
progesterone, such as 5-dehydroprogesterone,
6-dehydro-retroprogesterone (dydrogesterone), allopregnanolone
(allopregnan-3.alpha., or 3.beta.-ol-20-one), ethynodiol diacetate,
hydroxyprogesterone caproate (pregn-4-ene-3,20-dione,
17-(1-oxohexy)oxy); levonorgestrel, norethindrone, norethindrone
acetate (19-norpregn-4-en-20-yn-3-one,
17-(acetyloxy)-,(17.alpha.)-); norethynodrel, norgestrel,
pregnenolone, and megestrol acetate. Useful progestins also can
include allopregnone-3.alpha. or 3.beta., 20.alpha. or
20.beta.-diol (see Merck Index 258-261);
allopregnane-3.beta.,21-diol-11,20-dione;
allopregnane-3.beta.,17.alpha.-diol-20-one; 3,20-allopregnanedione,
allopregnane, 3.beta.,11.beta.,17.alpha.,20.beta.,21-pentol;
allopregnane-3.beta.,17.alpha.,20.beta.,21-tetrol;
allopregnane-3.alpha. or
3.beta.,11.beta.,17.alpha.,21-tetrol-20-one,
allopregnane-3.beta.,17.alpha. or 20.beta.-triol;
allopregnane-3.beta.,17.alpha.,21-triol-11,20-dione;
allopregnane-3.beta.,11.beta.,21-triol-20-one;
allopregnane-3.beta.,17.alpha.,21-triol-20-one;
allopregnane-3.alpha. or 3.beta.-ol-20-one; pregnanediol;
3,20-pregnanedione; pregnan-3.alpha.-ol-20-one;
4-pregnene-20,21-diol-3,11-dione; 4-pregnene-11.beta.,
17.alpha.,20.beta.,21-tetrol-3-one;
4-pregnene-17.alpha.,20.beta.,21-triol-3,11-dione;
4-pregnene-17.alpha.,20.beta.,21-triol-3-one, and pregnenolone
methyl ether. Further progestin derivatives include esters with
non-toxic organic acids such as acetic acid, benzoic acid, maleic
acid, malic acid, caproic acid, citric acid and the like. Inorganic
salts include, for example, hydrochloride, sulfate, nitrate,
bicarbonate and carbonate salts. Additionally, compounds that may
find use in the present invention include the progestin derivatives
that are disclosed in U.S. Pat. No. 5,232,917, herein incorporated
by reference.
[0027] The progestin or progestin metabolite may be administered
per se or in the form of a pharmaceutically acceptable salt. When
used in medicine, the salts of the progestin or progestin
metabolite should be both pharmacologically and pharmaceutically
acceptable, but non-pharmaceutically acceptable salts may
conveniently be used to prepare the free active compound or
pharmaceutically acceptable salts thereof and are not excluded from
the scope of this invention. Such pharmacologically and
pharmaceutically acceptable salts can be prepared by reaction of a
progestin or progestin metabolite with an organic or inorganic
acid, using standard methods detailed in the literature. Examples
of pharmaceutically acceptable salts are organic acids salts formed
from a physiologically acceptable anion, such as, tosglate,
methenesulfurate, acetate, citrate, malonate, tartarate, succinate,
benzoate, etc. Inorganic acid salts can be formed from, for
example, hydrochloride, sulfate, nitrate, bicarbonate and carbonate
salts. Also, pharmaceutically acceptable salts can be prepared as
alkaline metal or alkaline earth salts, such as sodium, potassium,
or calcium salts of the carboxylic acid group.
[0028] A traumatic injury to the CNS is characterized by a physical
impact to the central nervous system. For example, a traumatic
brain injury results when the brain is subjected to a physical
force that results in progressive neuronal cell damage and/or cell
death. A traumatic brain injury may result from a blow to the head
and manifests as either an open or closed injury. For example,
blast injuries are caused by the complex pressure wave generated by
an explosion, and can include closed injuries such as concussion
without external signs of head trauma. Other physical forces that
may act on the brain include increased intracranial pressure due
to, for example, subarachnoid or intracranial hemorrhage, tumor
growth, ventriculomegaly, or cerebral edema. Severe brain damage
can occur from lacerations, skull fractures, and conversely, even
in the absence of external signs of head injury. The physical
forces resulting in a traumatic brain injury cause their effects by
inducing three types of injury: skull fracture, parenchymal injury,
and vascular injury.
[0029] Parenchymal injuries include concussion, direct parenchymal
injury and diffuse axonal injury. Concussions are characterized as
a clinical syndrome of alteration of consciousness secondary to
head injury typically resulting from a change in the momentum of
the head (movement of the head arrested against a ridged surface).
The pathogenesis of sudden disruption of nervous activity is
unknown, but the biochemical and physiological abnormalities that
occur include, for example, depolarization due to excitatory amino
acid-mediated ionic fluxes across cell membranes, depletion of
mitochondrial adenosine triphosphate, and alteration in vascular
permeability. Postconcussive syndrome may show evidence of direct
parenchymal injury, but in some cases there is no evidence of
damage.
[0030] Contusion and lacerations are conditions in which direct
parenchymal injury of the brain has occurred, either through
transmission of kinetic energy to the brain and bruising analogous
to what is seen in soft tissue (contusion) or by penetration of an
object and tearing of tissue (laceration). A blow to the surface of
the brain leads to rapid tissue displacement, disruption of
vascular channels, and subsequent hemorrhage, tissue injury and
edema. Morphological evidence of injury in the neuronal cell body
includes pyknosis of nucleus, eosinophilia of the cytoplasm, and
disintegration of the cell. Furthermore, axonal swelling can
develop in the vicinity of damage neurons and also at great
distances away from the site of impact. This phenomenon can be
characterized as "diffuse neuronal injury" and is caused by
stretching and shearing of the axon. The inflammatory response to
the injured tissue follows its usual course with neutrophiles
preceding the appearance of macrophages.
[0031] An ischemic injury to the CNS is characterized by an
insufficiency or interruption in the blood supply to any locus of
the brain such as, but not limited to, a locus of the cerebrum,
cerebellum or brain stem. The spinal cord, which is also a part of
the CNS, is equally susceptible to ischemia resulting from
diminished blood flow. An ischemic episode may be caused by a
constriction or obstruction of a blood vessel, as occurs in the
case of a thrombus or embolus. Alternatively, the ischemic episode
may result from any form of compromised cardiac function, including
cardiac arrest. Where the deficiency is sufficiently severe and
prolonged, it can lead to disruption of physiologic function,
subsequent death of neurons, and necrosis (infarction) of the
affected areas. The extent and type of neurologic abnormality
resulting from the injury depend on the location and size of the
infarct or the focus of ischemia. Where the ischemia is associated
with a stroke, it can be either global or focal in extent.
[0032] Global ischemia, as used herein in reference to the CNS,
refers to a condition that results from a general diminution of
blood flow to the entire brain, forebrain, or spinal cord, which
causes the delayed death of neurons, particularly those in
metabolically active loci, throughout these tissues.
[0033] Focal ischemia, as used herein in reference to the CNS,
refers to a condition that results from the blockage of a single
artery that supplies blood to the brain or spinal cord, resulting
in the death of all cellular elements (pan-necrosis) in the
territory supplied by that artery.
[0034] As described above, the present invention provides a method
for treating or preventing neuronal damage caused by a traumatic or
ischemic injury to the CNS through the administration of a
therapeutically effective amount of a progestin or progestin
metabolite such that, prior to termination of administration of the
progestin or progestin metabolite the administration is tapered to
avoid withdrawal. As described in more detail in the Experimental
Section below, the present invention relates to the finding that,
when stopping progesterone therapy, tapered administration of
progesterone to avoid withdrawal results in greater efficacy of
progesterone therapy compared to abrupt termination of
administration.
[0035] By "tapered administration" or "tapered administration
dosing regimen" is meant successive reduced doses and eventual
elimination of the progestin or progestin metabolite, either over a
fixed period of time or a time determined empirically by a
physician's assessment based on regular monitoring of a therapeutic
response of a patient to a traumatic or ischemic CNS injury. The
period of the tapered progestin or progestin metabolite
administration can be about 12, 24, 36, 48 hours or longer.
Alternatively, the period of the tapered progestin or progestin
metabolite administration can range from about 1 to 12 hours, about
12 to about 48 hours, or about 24 to about 36 hours. In one aspect
of the invention, tapered administration of a progestin or
progestin metabolite involves tapered administration of
progesterone.
[0036] The drug taper employed could involve progressively dividing
administered doses by 50%. For example, such a taper from 500 mg
would go 500, 250, 125, 62.5, etc. The drug taper employed could be
a "linear" taper. For example, a "10%" linear taper from 500 mg
would go 500, 450, 400, 350, 300, 250, 200, 150, 100, 50, etc.
Alternatively, an exponential taper could be employed which, if the
program outlined above is used as an example, the exponential taper
would be, e.g., 500, 450, 405, 365, 329, 296, 266, 239, etc.
Accordingly, about a 5%, 10%, 20%, 30%, or 40% linear or
exponential taper could be employed in the methods of the
invention. In addition, a linear or exponential taper of about 1%
to 5%, about 6% to 10%, about 11% to 15%, about 16% to 20%, about
21% to 25%, about 26% to 30%, about 31% to 35%, about 36% to 40%
could be employed. Alternatively, the taper schedule can be
determined based on the treating physician's assessment of the
patient's response to therapy.
[0037] The tapered administration methods of the present invention
are used in combination with administration of progestin or
progestin metabolite therapies for subjects having traumatic or
ischemic CNS injury. As defined herein, the subject can be any
mammal, preferably a human or an animal, including domestic,
agricultural, or exotic animals. In specific embodiments, the human
is an adult (over 18 years of age), while in other embodiments, the
human is a child (under 18 years of age). The child can be a
neonate, infant, toddler, pre-pubescent or post-pubescent and range
in age from about birth, 1 month to about 2 year, about 1 year to
about 5 years, about 4 years to about 9 years, about 8 years to
about 14, or about 13 to about 18 years of age. In addition, the
human can be about 55 to 60, 60 to 65, 65 to 70, 70 to 75, 75 to
80, 80 to 85, 85 to 90, 90 to 95 or older.
[0038] Prior to the tapered administration of the present
invention, the progestin or progestin metabolite is administered at
a therapeutically effective level to a subject in need thereof for
the treatment of a CNS injury. By "therapeutically effective
amount" is meant the concentration of a progestin or progestin
metabolite that is sufficient to elicit a therapeutic effect. Thus,
the concentration of a progestin or progestin metabolite in an
administered dose unit in accordance with the present invention is
effective in the treatment or prevention of neuronal damage that
follows a traumatic or ischemic injury to the CNS and hence,
elicits a neuroprotective effect. The therapeutically effective
amount will depend on many factors including, for example, the
specific activity of the progestin or progestin metabolite, the
severity, pattern, and type of injury (e.g., traumatic or
ischemic), the resulting neuronal damage, the responsiveness of the
patient, the weight of the patient along with other intraperson
variability, the method of administration, and the progestin or
progestin metabolite formulation used. Various methods for
administering a therapeutically effective amount of the progestin
or progestin metabolite treat CNS injury, including determination
of efficacy, dosage, and route of administration, are known in the
art (see, e.g., U.S. Patent Application No. 60/664,728 filed Mar.
24, 2005, and U.S. patent application Ser. No. 09/973,375, filed
Oct. 9, 2001, both of which are herein incorporated by reference).
Any therapeutic protocol or regimen for the administration of a
therapeutically effective amount of progestin or progestin
metabolite to treat a traumatic or ischemic CNS injury may be used
in combination with the tapered administration method of the
present invention.
[0039] In one embodiment of the invention, the tapered
administration methods of the present invention are used in
combination with administration of progestin or progestin
metabolite at least once a day, including administration once or
several times a day. The duration of the treatment may be once per
day for a period of from two to three weeks and may continue for a
period of months or even years. The daily dose can be administered
either by a single dose in the form of an individual dosage unit or
several smaller dosage units or by multiple administration of
subdivided dosages at certain intervals.
[0040] For instance, a dosage unit can be administered from about 0
hours to about 1 hr, about 1 hr to about 24 hours, about 1 to about
72 hours, about 1 to about 120 hours, or about 24 hours to at least
about 120 hours post injury. Alternatively, the dosage unit can be
administered from about 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12,
13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 30, 40, 48, 72, 96,
120 hours or longer post injury. Subsequent dosage units can be
administered any time following the initial administration such
that a therapeutic effect is achieved. For instance, additional
dosage units can be administered to protect the patient from the
secondary wave of edema that may occur over the first several days
post-injury.
[0041] In another embodiment of the invention, the tapered
administration methods of the present invention are used in
combination with a constant progesterone or synthetic progestin
dosing regimen. By "constant progesterone or synthetic progestin
dosing regimen" is intended the patient undergoing therapy with the
progesterone or synthetic progestin is administered a constant
total hourly dose of the progesterone or synthetic progestin over
the course of treatment. This hourly dose of the progesterone or
synthetic progestin is partitioned into a series of equivalent
doses that are administered according to an appropriate dosing
schedule depending on the method of administration. The duration of
the constant progesterone or synthetic progestin dosing regimen is
about 12, 24, 36, 60, 72, 84, or 120 hours or about 1 to 24 hours,
about 12 to 36 hours, about 24 to 48 hours, about 36 to 60 hours,
about 48 to 72 hours, about 60 to 96 hours, about 72 to 108 hours,
about 96 to 120 hours, or about 108 to 136 hours.
[0042] In other embodiments of the invention, the tapered
administration methods of the present invention are used in
combination with a "two-level progesterone or synthetic progestin
dosing regimen" By "two-level progesterone or synthetic progestin
dosing regimen" is intended the patient undergoing the therapy with
the progesterone or synthetic progestin is administered the
progesterone or synthetic progestin during two time periods of
progesterone or synthetic progestin dosing. The two-time periods
can have a combined duration of about 12 hours to about 7 days,
including, 1, 2, 3, 4, or 5 days or about 15, 15, 30, 35, 40, 45,
50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120,
125, 130, 135, 140, or 144 hours or about 1 to 24 hours, about 12
to 36 hours, about 24 to 48 hours, about 36 to 60 hours, about 48
to 72 hours, about 60 to 96 hours, about 72 to 108 hours, about 96
to 120 hours, or about 108 to 136 hours. In one embodiment, the
two-level progesterone or synthetic progestin dosing regimen has a
combined duration of about 1 day to about 5 days; in other
embodiments, the two-level progesterone or synthetic progestin
dosing regimen has a combined duration of about 1 day to about 3
days.
[0043] In one embodiment, the total hourly dose of the progesterone
or synthetic progestin that is to be administered during the first
and second time periods of the two-level progesterone or synthetic
progestin dosing regimen is chosen such that a higher total hourly
dose of the progesterone or synthetic progestin is given during the
first time period and a lower hourly dose of the progesterone or
synthetic progestin is given during the second time period. The
duration of the individual first and second time periods of the
two-level progesterone or synthetic progestin dosing regimen can
vary, depending upon the health of the individual and history of
the traumatic or ischemic injury. Generally, the patient is
administered higher total hourly dose of progesterone or synthetic
progestin for at least 1, 2, 3, 4, 5, 6, 12 or 24 hours out of the
1 day to 5 day two-level progesterone or synthetic progestin dosing
regimen. The length of the second time period can be adjusted
accordingly, and range for example, from about 12 hrs, 24 hrs, 36
hrs, 48 hrs, 60 hrs, 72 hrs, 84 hrs, 96 his, 108 hrs, 120 his or
about 12 to about 36 his, about 24 to about 36 hrs, about 24 to
about 48 hrs, about 36 hrs to about 60 hours, about 48 his to about
72 hrs, about 60 hrs to about 84 hours, about 72 hrs to about 96
hrs, or about 108 hrs to about 120 hrs. Thus, for example, where
the two-level progesterone or synthetic progestin dosing regimen
has a combined duration of 3 days, the higher total doses of the
progesterone or synthetic progestin could be administered for the
first hour, and the lower total hourly dose of the progesterone or
synthetic progestin could be administered for hours 2 to 72.
[0044] In still further embodiments, the total hourly dose of
progesterone that is to be administered during the first and second
time periods of the two-level progesterone or synthetic progestin
dosing regimen is chosen such that a lower total hourly dose of the
progesterone or synthetic progestin is given during the first time
period and a higher hourly dose of the progesterone or synthetic
progestin is given during the second time period.
[0045] Area under the curve (AUC) refers to the area under the
curve that tracks the serum concentration (nmol/L) of the
progesterone or synthetic progestin over a given time following the
IV administration of the reference progesterone or synthetic
progestin standard. By "reference progesterone or synthetic
progestin standard" is intended the formulation of the progesterone
or synthetic progestin that serves as the basis for determination
of the total hourly progesterone or synthetic progestin dose to be
administered to a human patient with a traumatic or ischemic
central nervous system injury in accordance with the desired
constant or two-level progesterone or synthetic dosing regimen to
achieve the desired positive effect, i.e., a positive therapeutic
response that is improved with respect to that observed without
administration of the progesterone or synthetic progestin.
Accordingly, the total hourly dose of progesterone or synthetic
progestin to be administered during the constant or two-level
progesterone or synthetic progestin dosing regimen can therefore
allow for a final serum level of the progesterone or synthetic
progestin of about of about 100 ng/ml to about 1000 ng/ml, about
1100 ng/ml to about 1450 ng/ml, 100 ng/ml to about 250 ng/ml, about
200 ng/ml to about 350 ng/ml, about 300 ng/ml to about 450 ng/ml,
about 400 ng/ml to about 550 ng/ml, about 500 ng/ml to about 650
ng/ml, about 600 ng/ml to about 750 ng/ml, about 700 ng/ml to about
850 ng/ml, about 800 ng/ml to about 950 ng/ml, about 900 ng/ml to
about 1050 ng/ml, about 1000 ng/ml to about 1150 ng/ml, about 1100
ng/ml to about 1250 ng/ml, about 1200 ng/ml to about 1350 ng/ml,
about 1300 ng/ml to about 1500 ng/m. In specific embodiments, the
serum level of the progesterone or synthetic progestin comprises
about 100 ng/ml, 250 ng/ml, 500 ng/ml, 750 ng/ml, 900 ng/ml, 1200
ng/ml, 1400 ng/ml, 1600 ng/ml.
[0046] The tapered administration methods of the present invention
also contemplate embodiments where a patient undergoing a constant
progesterone or synthetic progestin therapy or a two-level
progesterone or synthetic dosing regimen is given a time period off
from progesterone or synthetic dosing. For example, when a
progesterone or synthetic progestin dosing regimen is performed,
the time period off from the progesterone or synthetic progestin
can occur between the conclusion of the first time period of the
two-level progesterone or synthetic progestin dosing regimen and
the initiation of the second time period of the two-level
progesterone or synthetic progestin dosing regimen. For example,
one could contemplate the first time period being administered in a
pre-hospital setting, for instance at the site of the trauma. The
second time period could then begin upon arrival at a hospital. In
these embodiments, the two-level progesterone or synthetic
progestin dosing regimen is interrupted such that progesterone or
synthetic progestin dosing is withheld for a period of about 15
minutes, 30 minutes, 1 hr, 2 his, 3 hrs, 4 hrs, 5 hrs, 6 hrs or
more.
[0047] Where a patient undergoing therapy in accordance with the
previously mentioned dosing regimens exhibits a partial response,
or a relapse following completion of therapy, subsequent courses of
progesterone or synthetic progestin therapy may be needed to
achieve a partial or complete therapeutic response. Thus,
subsequent to a period of time off from treatment, which may have
comprised a constant progesterone or synthetic progestin dosing
regimen or a two-level progesterone or synthetic progestin dosing
regimen, a patient may receive one or more additional treatment
periods comprising either constant or two-level progesterone or
synthetic progestin dosing regimens. Such a period of time off
between treatment periods is referred to herein as a time period of
discontinuance. It is recognized that the length of the time period
of discontinuance is dependent upon the degree of patient response
(i.e., complete versus partial) achieved with any prior treatment
periods of the progesterone or synthetic progestin therapy. It is
further recognized that prior to a period of time off or
discontinuance, administration of the progesterone or synthetic
progestin therapy may be tapered.
[0048] For use with the tapered administration methods of the
present invention, multiple treatment sessions are referred to
herein as maintenance cycles, where each maintenance cycle
comprises a completed dosing regimen. By "completed two-level
dosing regimen" is intended the patient has been administered both
the first period and the second period of progesterone or synthetic
progestin dosing. The necessity for multiple maintenance cycles can
be assessed by monitoring the physiological and behavioral
improvement of the patient. The duration between maintenance cycles
can be about 1 hr, 15 hrs, 1 day, 2 day, 3 day, 4 day, 5 day, 6 day
or other such time periods falling within the range of about 1 day
to about 14 days.
[0049] For use in the tapered administration methods of the present
invention, progestin or progestin metabolite may further comprise
an inorganic or organic, solid or liquid, pharmaceutically
acceptable carrier. The carrier may also contain preservatives,
wetting agents, emulsifiers, solubilizing agents, stabilizing
agents, buffers, solvents and salts. Compositions may be sterilized
and exist as solids, particulants or powders, solutions,
suspensions or emulsions. In addition to the aforementioned
ingredients, the compositions of the invention may further include
one or more accessory ingredient(s) selected from the group
consisting of diluents, buffers, flavoring agents, binders,
disintegrants, surface active agents, thickeners, lubricants,
preservatives (including antioxidants) and the like.
[0050] The progestin or progestin metabolite can be formulated
according to known methods to prepare pharmaceutically useful
compositions, such as by admixture with a pharmaceutically
acceptable carrier vehicle. Suitable vehicles and their formulation
are described, for example, in Remington's Pharmaceutical Sciences
(16th ed., Osol, A. (ed.), Mack, Easton Pa. (1980)). In order to
form a pharmaceutically acceptable composition suitable for
effective administration, such compositions will contain an
effective amount of the progestin or progestin metabolite, either
alone, or with a suitable amount of carrier vehicle.
[0051] The pharmaceutically acceptable carrier will vary depending
on the method of drug administration and may be, for example,
either a solid, liquid, or time release. Representative solid
carriers are lactose, terra alba, sucorse, talc, geletin, agar,
pectin, acacia, magnesium stearate, stearic acid, microcrystalin
cellulose, polymer hydrogels, and the like. Typical liquid carriers
include syrup, peanut oil, olive oil, cyclodextrin, and the like
emulsions. Those skilled in the art are familiar with appropriate
carriers for each of the commonly utilized methods of
administration. Furthermore, it is recognized that the total amount
of progestin or progestin metabolite administered as a therapeutic
effective dose will depend on both the pharmaceutical composition
being administered (i.e., the carrier being used) and the mode of
administration.
[0052] Compositions for use in the methods of the present invention
include those suitable for oral, rectal, topical, nasal,
ophthalmic, or parenteral (including intraperitoneal, intravenous,
subcutaneous, or intramuscular injection) administration. The
compositions may conveniently be presented in unit dosage form and
may be prepared by any of the methods well known in the art of
pharmacy. All methods include the step of bringing the active agent
into association with a carrier that constitutes one or more
accessory ingredients. In general, the compositions are prepared by
uniformly and intimately bringing the active compound into
association with a liquid carrier, a finely divided solid carrier
or both, and then, if necessary, shaping the product into desired
formulations.
[0053] Compositions for oral administration may be presented as
discrete units such as capsules, cachets, tablets, lozenges, and
the like, each containing a predetermined amount of the active
agent as a powder or granules; or a suspension in an aqueous liquor
or non-aqueous liquid such as a syrup, an elixir, an emulsion, a
draught, and the like.
[0054] A tablet may be made by compression or molding, optionally
with one or more accessory ingredients. Compressed tablets may be
prepared by compressing in a suitable machine, with the active
compound being in a free-flowing form such as a powder or granules
which is optionally mixed with a binder, disintegrant, lubricant,
inert diluent, surface active agent or dispersing agent. Molded
tablets comprised with a suitable carrier may be made by molding in
a suitable machine.
[0055] A syrup may be made by adding the active compound to a
concentrated aqueous solution of a sugar, for example sucrose, to
which may also be added any accessory ingredient(s). Such accessory
ingredients may include flavorings, suitable preservatives, an
agent to retard crystallization of the sugar, and an agent to
increase the solubility of any other ingredient, such as polyhydric
alcohol, for example, glycerol or sorbitol.
[0056] Formulations suitable for parental administration
conveniently comprise a sterile aqueous preparation of the active
compound, which can be isotonic with the blood of the
recipient.
[0057] Nasal spray formulations comprise purified aqueous solutions
of the active agent with preservative agents and isotonic agents.
Such formulations are preferably adjusted to a pH and isotonic
state compatible with the nasal mucous membranes.
[0058] Formulations for rectal administration may be presented as a
suppository with a suitable carrier such as cocoa butter, or
hydrogenated fats or hydrogenated fatty carboxylic acids.
[0059] Ophthalmic formulations are prepared by a similar method to
the nasal spray, except that the pH and isotonic factors are
preferably adjusted to match that of the eye.
[0060] Topical formulations comprise the active compound dissolved
or suspended in one or more media such as mineral oil, petroleum,
polyhydroxy alcohols or other bases used for topical formulations.
The addition of other accessory ingredients as noted above may be
desirable.
[0061] Further, compositions for use in the methods of the present
invention include liposomal formulations. The technology for
forming liposomal suspensions is well known in the art. When the
progestin or progestin metabolite salt thereof is an
aqueous-soluble salt, using conventional liposome technology, the
same may be incorporated into lipid vesicles. In such an instance,
due to the water solubility of the compound or salt, the compound
or salt will be substantially entrained within the hydrophilic
center or core of the liposomes. The lipid layer employed may be of
any conventional composition and may either contain cholesterol or
may be cholesterol-free. When the compound or salt of interest is
water-insoluble, again employing conventional liposome formation
technology, the salt may be substantially entrained within the
hydrophobic lipid bilayer that forms the structure of the liposome.
In either instance, the liposomes that are produced may be reduced
in size, as through the use of standard sonication and
homogenization techniques. The liposomal formulations containing
the progestin or progestin metabolite or salts thereof, may be
lyophilized to produce a lyophilizate which may be reconstituted
with a pharmaceutically acceptable carrier, such as water, to
regenerate a liposomal suspension.
[0062] Pharmaceutical formulations for use in the methods of the
present invention also include those which are suitable for
administration as an aerosol, by inhalation. These formulations
comprise a solution or suspension of the desired progestin or
progestin metabolite or a salt thereof or a plurality of solid
particles of the compound or salt. The desired formulation may be
placed in a small chamber and nebulized. Nebulization may be
accomplished by compressed air or by ultrasonic energy to form a
plurality of liquid droplets or solid particles comprising the
compounds or salts.
[0063] Further pharmaceutical formulations for use in the methods
of the present invention include controlled release preparations.
Such controlled release preparations may be achieved by the use of
polymers to complex or absorb the progestin or progestin
metabolite. The controlled delivery may be exercised by selecting
appropriate macromolecules (for example, polyesters, polyamino
acids, polyvinyl pyrrolidone, ethylene-vinylacetate,
methylcellulose, carboxymethylcellulose, or protamine sulfate). The
rate of drug release may also be controlled by altering the
concentration of such macromolecules.
[0064] Another possible method for controlling the duration of
action comprises incorporating the therapeutic agents into
particles of a polymeric substance such as polyesters, polyamino
acids, hydrogels, poly(lactic acid) or ethylene vinylacetate
copolymers. Alternatively, it is possible to entrap the therapeutic
agents in microcapsules prepared, for example, by coacervation
techniques or by interfacial polymerization, for example, by the
use of hydroxymethyl cellulose or gelatin-microcapsules or
poly(methylmethacrylate) microcapsules, respectively, or in a
colloid drug delivery system, for example, liposomes, albumin,
microspheres, microemulsions, nanoparticles, nanocapsules, or in
macroemulsions. Such teachings are disclosed in Remington's
Pharmaceutical Sciences (1980).
[0065] For use in the methods of the present invention,
compositions comprising a therapeutically effective concentration
of progestin or progestin metabolite may be administered using any
acceptable method known in the art. Thus, for example, the
pharmaceutical composition comprising progestin or progestin
metabolite can be administered methods that include intravenous
(IV), intramuscular (IM), subcutaneous (SC), intraperitoneal,
transdermal, buccal, vaginal, or intracerebroventricular
administration. When administered intravenously, the pharmaceutical
composition comprising progesterone or synthetic progestin can be
administered by infusion over a period of about 1 to about 120
hours. In some embodiments, infusion of progesterone or synthetic
progestin occurs over a period of about 24 to about 72 hours, over
a period of about 48 to about 96 hours, or over a period of about
24 to about 120 hours.
[0066] An embodiment of the present invention provides for the
administration of a progesterone or synthetic progestin or analogue
thereof via IV administration in a dose of about 0.1 ng to about
100 g per kg of body weight, about 10 ng to about 50 g per kg of
body weight, from about 100 ng to about 1 g per kg of body weight,
from about 1 .mu.g to about 100 mg per kg of body weight, from
about 1 fig to about 50 mg per kg of body weight, from about 1 mg
to about 500 mg per kg of body weight; and from about 1 mg to about
50 mg per kg of body weight. Alternatively, the amount of
progesterone or synthetic progestin administered to achieve a
therapeutic effective dose is about 0.1 ng, 1 ng, 10 ng, 100 ng, 1
.mu.g, 10 .mu.g, 100 .mu.g, 1 mg, 2 mg, 3 mg, 4 mg, 5 mg, 6 mg, 7
mg, 8 mg, 9 mg, 10 mg, 11 mg, 12 mg, 13 mg, 14 mg, 15 mg, 16 mg, 17
mg, 18 mg, 19 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg,
90 mg, 100 mg, 500 mg per kg of body weight or greater.
[0067] In another embodiment of the present invention provides for
the administration of a progestin or progestin metabolite or
analogue thereof via parenteral administration in a dose of about
0.1 ng to about 100 g per kg of body weight, about 10 ng to about
50 g per kg of body weight, from about 100 ng to about 1 g per kg
of body weight, from about 1 .mu.g to about 100 mg per kg of body
weight, from about 1 .mu.g to about 50 mg per kg of body weight,
from about 1 mg to about 500 mg per kg of body weight; and from
about 1 mg to about 50 mg per kg of body weight. Alternatively, the
amount of progestin or progestin metabolite administered to achieve
a therapeutic effective dose is about 0.1 ng, 1 ng, 10 ng, 100 ng,
1 .mu.g, 10 .mu.g, 100 .mu.g, 1 mg, 2 mg, 3 mg, 4 mg, 5 mg, 6 mg, 7
mg, 8 mg, 9 mg, 10 mg, 11 mg, 12 mg, 13 mg, 14 mg, 15 mg, 16 mg, 17
mg, 18 mg, 19 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg,
90 mg, 100 mg, 500 mg per kg of body weight or greater. In one
aspect of the invention, the progestin or progestin metabolite for
parenteral administration is progesterone or allopregnanolone.
[0068] In further embodiments of the present invention, the tapered
administration methods of the invention are used in combination
with the use of a progestin or progestin metabolite and at least
one additional neuroprotective agent to enhance neuroprotection
following a traumatic or ischemic CNS injury. Such agents include,
for example, any combination of progestin or progestin metabolite.
Other neuroprotective agents of interest include, for example,
compounds that reduce glutamate excitotoxicity and enhance neuronal
regeneration. Such agents may be selected from, but not limited to,
the group comprising growth factors. By "growth factor" is meant an
extracellular polypeptide-signaling molecule that stimulates a cell
to grow or proliferate. Preferred growth factors are those to which
a broad range of cell types respond. Examples of neurotrophic
growth factors include, but are no limited to, fibroblast growth
factor family members such as basic fibroblast growth factor (bFGF)
(Abraham et al. (1986) Science 233:545-48), acidic fibroblast
growth factor (aFGF) (Jaye et al. (1986) Science 233:541-45), the
hst/Kfgf gene product, FGF-3 (Dickson et al. (1987) Nature
326-833), FGF-4 (Zhan et al. (1988) Mol. Cell. Biol. 8:3487-3495),
FGF-6 (deLapeyriere et al. (1990) Oncogene 5:823-831), keratinocyte
growth factor (KGF) (Finch et al. (1989) Science 245:752-755), and
androgen-induced growth factor (AIGF) (Tanaka et al. (1992) Proc.
Natl. Acad. Sci. USA 89:8928-8923).
[0069] Additional neuroprotective agents include, ciliary
neurotrophic factor (CNTF), nerve growth factor (NGF) (Seiler, M.
(1984) Brain Research 300:33-39; Hagg T. et al. (1988) Exp Neurol
101:303-312; Kromer L. F. (1987) Science 235:214-216; and Hagg T.
et al. (1990) J. Neurosci 10(9):3087-3092), brain derived
neurotrophic factor (BDNF) (Kiprianova, I. et al. (1999) J.
Neurosci. Res. 56:21-27), Neurotrophin 3 (NT3), Neurotrophin 4
(NT4), transforming growth factor-.beta.1 (TGF-.beta.1)
(Henrick-Noack, P. et al. (1996) Stroke 27:1609-14), bone
morphogenic protein (BMP-2) (Hattori, A. et al. (1999) J.
Neurochem. 72:2264-71), glial-cell line derived neurotrophic factor
(GDNF) (Miyazaki, H. et al. (1999) Neuroscience 89:643-7),
activity-dependant neurotrophic factor (ADNF) (Zamostiano, R. et
al. (1999) Neurosci Letter 264:9-12), cytokine leukemia inhibiting
factor (LIF) (Blesch, A. et al. (1999) J. Neurosci. 19:3356-66),
oncostatin M, interleukin, and the insulin-like growth factors 1
and 2.
[0070] Other forms of neuroprotective therapeutic agents include,
for example, Clomethiazole (Zendra) (Marshal, J. W. et al. (1999)
Exp. Neurol. 156:121-9); kylnurenic acid (KYNA) (Salvati, P. et al.
(1999) Prog Neruopsychopharmacol Biol Psychiatry 23:741-52), Semax
(Miasoedova, N. F. et al. (1999) Zh Neurol Psikhiatr Imss Korsakova
99:15-19), FK506 (tacrolimus) (Gold, B. G. et al. (1999) J.
Pharmacol. Exp. Ther. 289:1202-10),
L-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (Inokuchi,
J. et al. (1998) Act Biochim Pol 45:479-92),
andrenocorticotropin-(4-9) analoge (ORG 2766) and dizolcipine
(MK-801) (Herz, R. C. et al. (1998) Eur J. Pharmacol 346:159-65),
cerebral interleukin-6) (Loddick, S. A. et al. (1998) J. Cereb
Blood Flow Metab 18:176-9), selegiline (Semkova, I. et al. (1996)
Eur J. Pharmacol 315:19-30), MK-801 (Barth, A. et al. (1996) Neuro
Report 7:1461-4; glutamate antagonist such as, NPS1506, GV1505260,
MK801 (Baumgartner, W. A. et al.(1999) Ann Thorac Surg 67:1871-3),
GV150526 (Dyker, A. G. et al. (1999) Stroke 30:986-92); AMPA
antagonist such as NBQX (Baumgartner, W. A. (1999) et al. Ann
Thorac Surg 67:1871-3, PD152247 (PNQX) (Schielke, G. P. et al.
(1999) Stroke 30:1472-7), SPD 502 (Nielsen, E. O. et al. (1999) J.
Pharmacol Exp Ther 289:1492-501), LY303070 and LY300164 (May, P. C.
et al. (1999) Neuroscience Lett 262:219-221).
[0071] Where the tapered administration methods of the invention
are used in combination with the use of a progestin or progestin
metabolite and at least one additional neuroprotective agent to
enhance neuroprotection following a traumatic or ischemic CNS
injury, it is recognized that even less of the progestin or
progestin metabolite may be required to be therapeutically
effective.
[0072] The methods of the present invention find use in treating a
traumatic or ischemic injury of the central nervous system. Methods
to quantify the extent of central nervous system damage (i.e.,
neurodegeneration) and to determine if neuronal damage was treated
or prevented following the administration of a progestin or
progestin metabolite are well known in the art. Such
neuroprotective effects can be assayed at various levels,
including, for example, by promoting behavioral and morphological
(i.e., enhancing tissue viability) recovery after traumatic or
ischemic brain injury. A variety of anatomical, immunocytochemical
and immunological assays to determine the effect of the progestin
or progestin metabolite on necrosis, apoptosis, and neuronal glial
repair are known in the art. As such, the neuroprotection resulting
from the methods of the present invention will result in at least
about a 10% to 20%, 20% to 30%, 30% to 40%, 40% to 60%, 60% to 80%
or greater increase in neuronal survival and/or behavioral recovery
as compared to the control groups.
[0073] Histological and molecular marker assays for an increase in
neuronal survival are known. For example, Growth Associated Protein
43 (GAP-43) can be used as a marker for new axonal growth following
a CNS insult. See, for example, Stroemer et al. (1995) Stroke
26:2135-2144, Vaudano et al. (1995) J. of Neurosci. 15:3594-3611.
Other histological markers can include a decrease in astrogliosis
and microgliosis. Alternatively, a delay in cellular death can be
assayed using TUNEL labeling in injured tissue. Further anatomical
measures that can be used to determine an increase in
neuroprotection include counting specific neuronal cell types to
determine if the progestin or progestin metabolite is
preferentially preserving a particular cell type (e.g., cholinergic
cells) or neurons in general.
[0074] In addition, behavioral assays can be used to determine the
rate and extent of behavior recovery in response to the treatment.
Improved patient motor skills, spatial learning performance,
cognitive function, sensory perception, speech and/or a decrease in
the propensity to seizure may also be used to measure the
neuroprotective effect. Such functional/behavioral tests used to
assess sensorimotor and reflex function are described in, for
example, Bederson et al. (1986) Stroke 17:472-476, DeRyck et al.
(1992) Brain Res. 573:44-60, Markgraf et al. (1992) Brain Res.
575:238-246, Alexis et al. (1995) Stroke 26:2336-2346; all of which
are herein incorporated by reference. Enhancement of neuronal
survival may also be measured using the Scandinavian Stroke Scale
(SSS) or the Barthl Index. Behavioral recovery can be further
assessed using the recommendations of the Subcommittee of the NODS
Head Injury Centers in Humans (Hannay et al. (1996) J. Head Trauma
Rehabil. 11:41-50), herein incorporated by reference. Behavioral
recovery can be further assessed using the methods described in,
for example, Beaumont et al. (1999) Neurol. Res. 21:742-754; Becker
et al. (1980) Brain Res. 200:07-320; Buresov et al. (1983)
Techniques and Basic Experiments for the Study of Brain and
Behavior; Kline et al. (1994) Pharmacol. Biochem. Behav.
48:773-779; Lindner et al. (1998) J. Neurotrauma 15:199-216; Morris
(1984)J. Neurosci. Methods 11:47-60; Schallert et al. (1983)
Pharmacol. Biochem. Behav. 18:753-759.
[0075] It is recognized that a traumatic injury to the CNS results
in multiple physiological events that impact the extent and rate of
neurodegeneration, and thus the final clinical outcome of the
injury. The treatment of a traumatic injury to the CNS, as defined
by the present invention, encompasses any reduction and/or
prevention in one or more of the various physiological events that
follow the initial impact. Hence, the methods of the invention find
use in the reduction and/or prevention of physiological events
leading to neurodegeneration following a traumatic injury to the
central nervous system.
[0076] For instance, cerebral edema frequently develops following a
traumatic injury to the CNS and is a leading cause of death and
disability. Cortical contusions, for example, produce massive
increases in brain tissue water content which, in turn, can cause
increased intracranial pressure leading to reduced cerebral blood
flow and additional neuronal loss. Hence, the methods of the
invention find use in reducing and/or eliminating cerebral edema
and/or reducing the duration of the edemic event following a
traumatic injury to the CNS. Assays to determine a reduction in
edema are known in the art and include, but are not limited to, a
decrease in tissue water content following the administration of
the progestin or progestin metabolite (Betz et al. (1990) Stroke
21:1199-204, which is herein incorporated by reference).
Furthermore, an overall improvement in behavioral recovery can also
be used as a measure for a decrease in edema. A decrease in edema
in the effected tissue by at least about 15% to 30%, about 30% to
45%, about 45% to 60%, about 60% to 80%, or about 80% to 95% or
greater will be therapeutically beneficial, as will any reduction
in the duration of the edemic event.
[0077] Vasogenic edema following a traumatic brain injury has been
associated with damage to the vasculature and disruption of the
blood-brain barrier (BBB) (Duvdevani et al. (1995) J. Neurotrauma
12:65-75, herein incorporated by reference). Progesterone has been
shown to reduce the permeability of the BBB to macromolecules, but
not ions, such as sodium in vitro (Betz et al. (1990) Stroke
21:1199-204; Beta et al. (1990) Acta. Neurochir. Suppl. 51:256-8;
both of which are herein incorporated by reference). Hence, the
methods of the invention find use in reducing or eliminating
vasogenic edema following a traumatic brain injury. Assays to
determine a decrease in vasogenic edema are known in the art and
include, for instance, a reduction in Evans' blue extravasation
after cortical contusion (Roof et al. (1994) Society for
Neuroscience 20:91, herein incorporated by reference).
[0078] Further physiological effects of a traumatic brain injury
include an immune response. See, for example, Soares et al. (1995)
J. Neurosci. 15:8223-33; Holmin et al. (1995) Acta Neurochir.
132:110-9; Arvin et al. (1996) Neurosci. Biobehav. Rev. 20:445-52.
Following a cortical impact, severe inflammatory reactions and
gliosis at the impact site and at brain areas distal to the primary
site of injury occurs. The inflammatory response is characterized
by the expression of adhesion molecules on the vascular surfaces,
resulting in the adherence of immune cells and subsequent
extravasation into the brain parenchyma. By releasing cytokines,
the invading macrophages and neutrophils stimulate reactive
astrocytosis. Release of different chemokines by other cell types
induces these immune cells to become phagocytic, with the
simultaneous release of free radicals and pro-inflammatory
compounds, e.g., cytokines, prostaglandins, and excitotoxins (Arvin
et al. (1996) Neurosci. Biobehav. Ref. 20:445-52; Raivich et al.
(1996) Kelo J. Med. 45:239-47; Mattson et al. (1997) Brain Res.
Rev. 23:47-61; all of which are herein incorporated by
reference).
[0079] The methods of the invention provide a means to reduce or
eliminate the inflammatory immune reactions that follow a traumatic
CNS injury. Furthermore, by reducing the inflammatory response
following an injury, the progestin or progestin metabolite of the
present invention can substantially reduce brain swelling and
intracranial pressure and reduce the amount of neurotoxic
substances (e.g., free radicals and excitotoxins) that are
released. Therefore, by reducing the immune/inflammatory response
following a traumatic injury to the CNS, neuronal survival and/or
behavioral recovery will be enhanced.
[0080] Assays that can be used to determine if the progestin or
progestin metabolite of the invention is imparting an
anti-inflammatory and a nonspecific suppressive effect on the
immune system following a traumatic CNS injury include, for
example, a reduction in cytokine induced microglial proliferation
in vitro (Hoffman et al. (1994) J. Neurtotrauma 11:417-31;
Garcia-Estrada et al. (1993) Brain Res. 628:271-8; both of which
are herein incorporated by reference); a reduction in the
generation of cytotoxic free radicals by activated macrophages
(Chao et al. (1994) Am. J. Reprod. Immunol. 32:43-52; Robert et al.
(1997) Nitric Oxide 1:453-62; Kelly et al. (1997) Biochem. Biophys.
Res. Commun. 239:557-61; Ganter et al. (1992) J. Neurosci. Res.
33:218-30; all of which are herein incorporated by reference); a
reduction in the expression of inducible nitric oxide synthetase
and the amount of nitric oxide release by macrophages (Robert et
al. (1997) Nitric Oxide 1:453-62; Miller et al. (1996) J. Leukoc.
Biol. 59:442-50; both of which are herein incorporated by
reference); the release of a "progesterone-induced blocking factor"
that inhibits natural killer cell activity Cheek et al. (1997) Am.
J. Reprod. Immunol. 37:17-20; Szekeres-Bartho et al. (1997) Cell
Immunol. 177:194-9; Szekeres-Bartho et al. (1996) Am. J. Reprod.
Immunol. 35:348-51; all of which are herein incorporated by
reference); a decrease in the number of GFAP-positive astrocytes
after brain injury which is suggestive of less secondary damage
(Garcia-Estrada et al. (1993) Brain Res. 628:271-8; Garcie-Estrada
et al (1999) Int. J. Dev. Neurosci. 17:145-51; Cheek et al. (1997)
Am. J. Reprod. Immunol. 37:17-20; Szekeres-Bartho et al. (1997)
Cell Immunol. 177:194-9; Szekeres-Bartho et al. (1996) Am. J.
Reprod. Immunol. 35:348-51; all of which are herein incorporated by
reference); a reduction in the number of inflammatory immune cells
(OX42-positive cells); a reduction in the loss of ChAT-positive and
COX-positive neurons; a reduction in the number of TUNEL-positive
and MnSOD-positive neurons; and an increase in the intensity of
succinate dehydrogenase and cytochrome oxidase activity.
[0081] Furthermore, a reduction in the inflammatory immune
reactions following a traumatic brain injury can be assayed by
measuring cytokine level following the injury in the sham controls
versus the progestin OT progestin metabolite treated subjects.
Cytokines are mediators of inflammation and are released in high
concentrations after brain injury. The level of pro-inflammatory
cytokines (e.g., interleukin 1-beta, tumor necrosis factor, and
interleukin 6) and the level of anti-inflammatory cytokines (e.g.,
interleukin 10 and transforming growth factor-beta) can be
measured. For instance, "real-time" polymerase chain reactions
(PCR) can be used to measure the strength of the mRNA signal and
ELISA can be used to determine protein levels. In addition,
histological analysis for different inflammatory cell types (e.g.,
reactive astrocytes, macrophages and microglia) can be used to
measure a reduction in the inflammatory response.
[0082] Another physiological consequence of a traumatic CNS injury
is an increase in lipid peroxidation. The methods of the invention
find use in reducing free radical damage and thus decreasing or
eliminating lipid peroxidation. This effect may occur through an
enhancement of endogenous free radical scavenging systems. Assays
to measure a reduction in lipid peroxidation in both brain
homogenate and in mitochondria are known in the art and include,
for example, the thiobarbituric acid method (Roof et al. (1997)
Mol. Chem. Neuropathol. 31: 1-11; Subramanian et al. (1993)
Neurosci. Lett. 155:151-4; Goodman et al. (1996) J. Neurochem.
66:1836-44; Vedder et al. (1999) J. Neurochem. 72:2531-8; all of
which are herein incorporated by reference) and various in vitro
free radical generating systems Furthermore, alterations in the
levels of critical free radical scavenger enzymes, such as
mitochondrial glutathione can be assayed. See, for example,
Subramanian et al. (1993) Neurosci. Lett. 155:151-4; and Vedder et
al. (1999) J. Neurochem. 72:2531-8; both of which are herein
incorporated by reference.
[0083] Furthermore, cultured, cytokine-stimulated macrophages
generate nitrite, superoxide, and hydrogen peroxide. Since
macrophages are known to be very active between 48 hours and seven
days after a traumatic brain injury, a reduction in these reactive
cells would reduce, secondary-damage to neurons. See, for example,
Fulop et al. (1992) 22.sup.nd Annual Meeting of the Society for
Neuroscience 18:178; Soares et al. (1995) J. Neurosci. 15: 8223-33;
Holmin et al. (1995) Acta Neurochir. 132:110-9; all of which are
herein incorporated by reference.
[0084] It is recognized that an ischemic injury to the CNS results
in its own set of physiological events that impact the extent and
rate of neurodegeneration, and thus the final clinical outcome of
the injury. The treatment of an ischemic injury to the CNS, as
defined by the present invention, encompasses any reduction and/or
prevention in one or more of the various physiological events that
follow the initial interruption in blood supply. Hence, the methods
of the invention find use in the reduction and/or prevention of
physiological events leading to or associated with
neurodegeneration following an ischemic injury to the central
nervous system.
[0085] As described elsewhere herein, ischemic CNS injury is
associated with certain physiological events leading to
neurodegeneration, including, for example, release or
overexpression of proteins such as NSE, myelin basic protein, GFAP,
the S-100 protein, and PKCg, stimulation of membrane phospholipid
degradation and subsequent free-fatty-acid accumulation, energy
failure due to ATP depletion, cellular acidosis, glutamate release
and excitotoxicity, calcium ion influx, and free radical
generation. Assays to determine a reduction and/or prevention of
physiological events leading to or associated with
neurodegeneration following an ischemic CNS injury may be directed
toward measuring any of these physiological events. For example,
assays for measuring levels of NSE, myelin basic protein, GFAP, the
S-100 protein, and PKCg are well known in the art (see, e.g.,
Missler et al. (1997) Stroke, 28:1956-1960; Shashoua et al. (1984)
J. Neurochem., 42:1536-1541; and U.S. Pat. No. 6,268,223; all of
which are incorporated herein by reference). Assays for measuring a
decrease in serum levels of fatty acids may be determined by
methods well known in the art such as taught in U.S. Pat. Nos.
4,071,413; 5,512,429; 5,449,607; and 4,369,250, all of which are
incorporated herein by reference.
[0086] Other assays for determining a reduction and/or prevention
of physiological events leading to or associated with
neurodegeneration following an ischemic CNS injury may be directed
toward clinical assessments of, for example, a decrease in infarct
area, improved body weight, and improved neurological outcome. Such
clinical assays are well known to those of skill in the art.
[0087] Having now generally described this invention, the same will
be better understood by reference to certain specific examples
which are included herein for purposes of illustration only, and
are not intended to be limiting of the invention, unless
specified.
EXPERIMENTAL
Example 1
Effects of Progesterone on Necrotic-Damage and Behavioral
Abnormalities Caused by TBI
Methods:
[0088] Male Sprague-Dawley rats (300 g) were housed individually in
wire cages and kept on a reverse light-dark cycle (0800-2000 h).
Animals were assigned to one of four groups: (1) lesion (n=7); (2)
lesion+3 days progesterone (LP3; n=7); (3) lesion+5 days
progesterone (LP5; n=7); and (4) Sham (n=8). All procedures
involving animals conformed to guidelines set forth in the Guide
for the Care and Use of Laboratory Animals (U.S. Department of
Health and Human Services, Pub no. 85-23, 1985) and were approved
by the Emory University Institutional Animal Care and Use
Committee.
[0089] Bilateral contusions of the medial prefrontal cortex were
created by a pneumatic impactor device as previously described
[40]. Briefly, rats were given anesthetized with ketamine/xylazine
(90 mg/kg; 10 mg/kg) and placed in a stereotaxic apparatus. A
craniectomy (diameter 6 nm u) was made over the midline of the
prefrontal cortex with its center 1.5 mm AP to bregma. After
removal of the bone, the tip of the impactor (diameter 5 mm) was
moved to +3.0 mm AP; 1.0 mm ML (from bregma), and checked for
adequate clearance. Trauma was produced by pneumatically activating
the piston to impact -2.0 mm DV (from dura) at a velocity of 3 m/s
with a brain contact time of 0.5 seconds.
[0090] Progesterone was dissolved in peanut oil (Sigma; 4 mg/kg)
and injections were given at 1 and 6 hours post-injury and then
once per day for either 3 or 5 consecutive days. Control animals
received injections of vehicle at similar time-points. Animals were
coded with regard to surgery and treatment to prevent experimenter
bias during behavioral testing and histological examination.
[0091] Twenty-one days after surgery, animals were perfused with
100 ml 0.1 M phosphate-buffered saline (PBS; pH 7.4) followed by
400 ml 4% paraformaldehyde in 0.1 M phosphate buffer (PB; pH 7.4).
Following cryoprotection in 30% sucrose, coronal 40-.mu.m-thick
sections were cut on a freezing microtome, immediately mounted on
gel-coated slides and stained for Nissl with thionine to determine
placement and extent of the injury.
[0092] Mean area measurements of lesion size were quantified from
sections at 15 rostral-caudal levels spaced 300 .mu.n apart. The
perimeter of the necrotic cavity (including injured penumbra) was
traced on digitized images using the Jandel Scientific SigmaScan
software calibrated to calculate the area in mm.sup.2 for each
level traced. Perimeters of the striatum and the lateral ventricles
were also traced and mean areas were quantified from 7
rostral-caudat levels (300 .mu.m apart).
[0093] Cell counts were done on an Olympus BH-2 microscope equipped
with an eyepiece micrometer grid (sample area=40 .mu.m.sup.2 at
.times.400 magnification). Bilateral cell counts of Nissl-stained
neurons were made on 3 separate sections in each of the following
areas: (1) STR (+1.8 to +1.2 mm AP), (2) GP (-0.3 to -1.2 mm AP),
(3) DMN (-2.3 to -2.9 mm AP), and (4) VMN (-2.3 to -2.9 mm AP).
Only cells with neuronal nuclei and intact membranes were counted
as neurons.
[0094] Experienced individuals who were blind to treatment
conditions of the study conducted all histological and behavioral
analyses. All data were tested for normality and homoschedasticity
before being analyzed by parametric analysis of variance (ANOVA).
MWM results were analyzed using separate mixed-factorial (4
groups.times.5 days) analysis of variance (ANOVA) on each of the
two 5-day testing periods (acquisition and retention respectively).
Results of the BSN task were analyzed using the mixed-factorial
ANOVA (4 groups.times.2 post-injury trials). Histological
comparisons on mean densitometry recordings, area measurements, and
cell counts were made using a one-way ANOVA. All between-group
comparisons were made using multiple Tukey post-hoc tests
(p<0.05) when the overall ANOVA was significant p<05) between
groups. Pearson r coefficients were calculated to determine whether
significant correlations could be detected between histological
(e.g., lesion size and cellular density) and behavioral parameters
(e.g., acquisition and retention of the MWM task and measures of
sensory neglect).
[0095] Beginning one week after surgery, spatial learning ability
was assessed in the Morris water maze (MWM) task described
previously. Each animal was tested for a total of 10 days in two
5-day trial blocks (acquisition and retention respectively).
Animals were placed in the pool (nose facing the pool-wall) at one
of four randomly determined starting positions (e.g.: N, S, E, W).
Each rat was allowed to swim freely in the pool until it found the
hidden platform or until 90 seconds had elapsed. If an animal did
not find the platform in 90 seconds, be was manually guided to it.
Once on the platform, animals were allowed to rest for 10 seconds
and then removed from the pool and placed near a heat lamp for
warmth. Each rat was given two trials per day with a 20-second
intertrial interval (ITI). The dependent measures for this task
were latency to find the hidden platform and swim strategy (e.g.,
percent of time spent in the inner vs. outer annuli). Swim speed
measures were recorded daily in order to delineate motor
dysfunction from learning impairment.
[0096] Measures of attentional abilities, using a bilateral sensory
neglect (BSN) task, were recorded one day prior to surgery
(baseline) and on postsurgical days 6 and 20. Pairs of circular
adhesive papers (2 cm dia) were attached to the distal-radial areas
of each forepaw and the rats' latencies to remove the stimuli were
recorded. Each rat was given four trials (2-min ITI) per testing
period with a maximum trial length of 2 minutes. If the rats did
not remove the adhesive disks within the standard time, a total
latency of 2 minutes was recorded for that trial.
Results:
[0097] Histology. In most animals, necrotic tissue was primarily
restricted to the medial prefrontal and cingulate cortex. However,
in some cases, more severe tissue damage extended into the corpus
callosum and the most dorsal aspects of the medial septum and
striatum (Data not shown). A significant main effect on necrotic
cavity formation was observed between the three injured groups,
(F.sub.2,19=3.57, P<0.05). Tukey post hoc analysis revealed a
dose-dependent reduction in necrotic cavity formation. Data not
shown. Notably, all animals that were given progesterone tended to
have smaller lesions compared to injured animals that were given
vehicle injections. However, only 5 days of progesterone resulted
in significant reductions in overall necrotic cavity formation
(P<0.05). We also observed enlargement of the lateral ventricles
in all injured groups as compared to control animals
(F.sub.3,25=5.28, P<0.01) but progesterone did not have any
effect on this measure. Data not shown. No between-group
differences were shown on measures of mean striatal area.
[0098] One-way ANOVA revealed a main effect of mean cellular
density between groups on counts taken in the STR
(F.sub.3,25=15.58, P<0.01), GP (F.sub.3,25=4.47, P<0.01), DMN
(F.sub.3,25=5.37, P<0.01), and VMN (F.sub.3,25=8.68, P<0.01).
Results of Tukey post hoc tests showed that both LP3 and LP5
treatments resulted in a significant reduction of injury-induced
neuronal loss in all brain regions examined. However, 5 days of
progesterone was more effective than 3 days at attenuating neuronal
loss in the VMN, the area most distal to injured penumbra. Data not
shown.
[0099] Behavioral Testing. In the MWM task, all of the injured
groups displayed deficits in spatial learning performance as
compared to control animals during the initial 5-day acquisition
phase (F.sub.3,25=19.45, P<0.01). However, Tukey post hoc tests
detected improved spatial learning performance in LP5, but not LP3,
animals during the second 5-day trial block (F.sub.3,25=6.76,
P<0.01). Data not shown.
[0100] ANOVA revealed a significant main effect on swim patterns
during acquisition (F.sub.3,25=28.23, P<0.01) and retention
(F.sub.3,25=12.25, P<0.01) of the MWM task. Data not shown. All
the injured animals displayed sustained thigmotaxic (wall-hugging)
swim patterns during the first 5-day MWM trial block. But a
reduction of thigmotaxic behavior was observed in the LP5-treated
animals in the last 2 days of the second phase of MWM testing
(P>0.05 compared to controls) corresponding with the reduction
in latency to find the platform observed in this group. There were
no between-group differences on swim speed measurements on any day
of testing.
[0101] There were no between-group differences on baseline measures
of sensory neglect recorded one day prior to surgery. A significant
main effect between groups (F.sub.3,25=6.17, P<0.01) was
observed in results of the BSN task following controlled cortical
contusion to the medial prefrontal cortex. Tukey post hoc analysis
showed that only the LP3-treated animals were impaired on this task
compared to control animals at both 6 and 20 days post injury (Data
not shown).
[0102] We also detected significant correlations between
histological measures and performance in the MWM task.
Specifically, there was a positive correlation between necrotic
cavity formation and improved MWM performance during the second
5-day trial block, suggesting that smaller lesions resulted in
improved retention of this task (r.sub.21=+0.44, P<0.05).
Similarly, we observed a negative correlation between cellular
density and spatial learning performance during the second phase of
MWM testing (r.sub.21=-0.50, P<0.05) which indicates that
progesterone-mediated neuronal sparing allowed for greater
functional recovery (data not shown). Finally, we did not observe
any significant correlations between either lesion size or cellular
density and measures of sensory neglect.
SUMMARY
[0103] The reduction of the injury-induced necrotic cavity
formation provides evidence that a post-injury neurosteriod
intervention might reduce lesion volume following TBI in this
animal model. In the present study, we observed a dose-dependent
reduction in necrotic cavity formation in progesterone treated
animals. Specifically, while the necrotic cavities in the brains of
animals treated with only 3 days of progesterone (LP3) tended to be
smaller than in the brains of injured animals, only the 5-day
treatment regimen (LP5) resulted in significantly smaller lesions.
Our study now provides the first evidence that progesterone may
also attenuate TBI-induced tissue loss.
[0104] In our study, progesterone also protected against secondary
cell loss in brain regions both proximal (e.g., STR) and distal
(e.g., GP, DMN, and VMN) to the zone of injury. Interestingly, in
the present study, both 3 and 5 days of progesterone treatment
reduced neuronal loss in the STR, GP, and DMN, but only
LP5-treatments produced significant reductions in cell loss of the
VMN compared to untreated controls.
[0105] And finally, in the present study, all injured groups were
impaired on the acquisition phase of MWM testing. The LP5 animals
showed clear improvement, albeit not to control levels, in spatial
performance during the retention phase of this task. Significant
correlations were found between neuropathological parameters (e.g.,
necrotic cavity formation and neuronal sparing) and MWM performance
demonstrating that progesterone-mediated reductions in lesion size
cell death resulted in concomitant reductions in latency to find
the platform.
Example 2
Dosage Response Curves for Behavioral Recovery Following TBI Upon
Administration of Progesterone in a Cylcodextrin Vehicle
Methods:
[0106] Surgery to induce a traumatic brain injury was performed as
outlined in Example 1. Behavior testing using the Morris Water
Maize was performed as outlined in Example 1 and the methods for
the tactical adhesive removal were performed.
Results:
[0107] FIGS. 1A and 1B demonstrate that low and moderate doses of
progesterone (8 mg/kg & 16 mg/kg in a cyclodextrin-containing
vehicle) produced consistent improvement in Morris water maze
performance, whereas the high dose of progesterone (32 mg/kg in a
cyclodextrin-containing vehicle) did not show any beneficial
effect.
[0108] The sticker removal task is a test for sensory neglect which
is a primary deficit for frontal injury. In this task all doses
initially produce behavioral recovery, however, the group receiving
the high dose of progesterone degraded to lesion control levels and
the moderate dose, which was initially at lesion control levels
improved to sham levels by day 21 post-injury. See FIG. 2.
Example 3
Tapered Progesterone Withdrawal Enhances Recovery after Traumatic
Brain Injury
Methods:
[0109] Male Sprague-Dawley rats received either medial frontal
cortex injury or sham surgery. Injections were given 1 and 6 hours
post-injury, and every 24 hours for 7 days. Treatment groups (n=8)
encompassed injured (1) and sham (S) acute withdrawal (AW), tapered
withdrawal (TW) and vehicle (V) treatments. TW injections were
progressively halved over the final two treatments. Behavioral
testing was conducted post-surgery, mid- and post-withdrawal.
Activity boxes were used to investigate vertical movements and
exploration. Sensory neglect and anxiety behaviors were also
analyzed. Brain harvesting was performed at 8 days or 3 weeks
post-injury. Perfused tissue sections were analyzed for lesion
volume and immunohistochemical response. Fresh brain tissue was
flash frozen in chilled 2-methyl butane, and then homogenized for
Western blot analysis.
Results:
[0110] Acute withdrawal and injury (AWI) interacted to increase
anxiety, locomotor and sensory deficits compared to tapered
progesterone withdrawal (TWI). Additionally, acute withdrawal-shams
(AWS) had increased motor impairments compared to all other shams,
and increased anxiety compared to tapered progesterone rats. The
neuroprotective factors BDNF and HSP70 increased for TWI over AWI
over VI at 3 weeks post-injury. This beneficial effect of tapered
hormone treatment correlated with lesion reconstruction and GFAP
staining; TWI animals had the smallest lesion volume and fewest
reactive astrocytes, followed by AWI, while VI had the largest
lesion volume and most reactive astrocytes. Apoptosis and
inflammation were decreased with TW, as demonstrated by p53, active
Caspase 3, TNF.alpha. and NF.kappa.B.
CONCLUSION
[0111] Acute PW has a compelling effect on both behavior and tissue
recovery after traumatic brain injury. At the peak of withdrawal,
animals undergoing progesterone withdrawal syndrome exhibit
increased anxiety, sensory deficits, and locomotor deficits; all of
these are further exacerbated by injury. One week later, increased
behavioral impairments are still evident in AWI animals. Western
blotting revealed decreased expression of apoptotic and
inflammatory proteins with tapered withdrawal, although all
progesterone treatments led to better outcomes compared to
vehicle-only controls. At 3 weeks post-injury, the compound effect
of lesions and acute progesterone withdrawal continued to cause
behavioral deficits over those animals with a gradual decrease in
progesterone treatment. These findings can be taken to suggest that
in clinical testing, tapered withdrawal of progesterone will be
more beneficial to CNS repair than an abrupt termination of the
treatment at the end of the dosage regime.
Example 4
Tapered Progesterone Withdrawal Promotes Long-term Recovery after
Traumatic Brain Injury
[0112] Having demonstrated that after TBI, AW causes an increase in
anxiety behaviors and cerebro-cellular inflammation compared to TW
(see Example 3), this study investigated the behavioral and
cellular effects of AW two weeks after termination of treatments to
determine the longer-term influence of withdrawal after injury.
[0113] As described above, progesterone treatment following
traumatic brain injury and stroke reduces the effects of secondary
injury and necrosis (Asbury et al. (1998) Behav. Brain Res.,
97:99-106; Attella et al. (1987) Behav. Neural. Biol., 48:352-367;
Chen et al. (1999) J. Neurol. Sci., 171:24-30; Galani et al. (2001)
Restor. Neurol. Neurosci., 18:161-166; Gibson et al. (2005) Exp.
Neurol., 193:522-530; Gibson and Murphy (2004) J. Cereb. Blood Flow
Metab., 24:805-813; Grossman et al. (2004) Brain Res., 1008:29-39;
Kumon et al. (2000) J. Neurosurg., 92:848-852; Roof et al. (1994)
Exp. Neurol., 129:64-69; Roof et al. (1994) "Progesterone Reduces
BBB Damage Following Bilateral, Medial Frontal Contusion," in
Twenty-first Annual Meeting of the Society for Neuroscience, Miami
Beach, Fla., p. 191; Roof et al. (1997) Mol. Chem. Neuropathol.,
31:1-11; Shear et al. (2002) Exp. Neurol., 178:59-67; Vink and Van
Den Heuvel (2004) Expert Opin. Investig. Drugs, 13:1263-1274). AW,
however, results in an increase in apoptosis, inflammation and
anxiety behaviors during the acute recovery phase after TBI
compared to TW (Cutler et al. (2005) Exp. Neurol., 195(2):423-429).
All animals given progesterone, regardless of their treatment
regime, showed improvement over vehicle-treated animals, but those
animals with TW had better recovery as evidenced by less
inflammation, apoptosis and functional anxiety. AW causes anxiety,
depression, and increased seizure susceptibility due to a sudden
decrease in GABA-A interactions with allopregnanolone, a
progesterone metabolite (Foldvary-Schaefer et al. (2004) Cleve.
Clin. J. Med., 71:S11-18; Gulinello et al. (2003) Eur. J.
Neurosci., 17:641-648; Kulkarni and Reddy (1995) Drugs Today,
31:433-455; Rupprecht (2003) Psychoneuroendocrinology, 28:139-168;
Smith (2002) Steroids, 67:519-528). The resulting increase in NMDA
activation leads to an excitatory neural environment (Lukasiuk and
Pitkanen (2000) J. Neurochem., 74:2445-2454; Van Den Pol et al.
(1996) Neuroscience, 74:653-674). Under the added stress of trauma,
this effect is amplified to an increased excitotoxicity. With
gradual withdrawal, this excitotoxicity, secondary injury and
inflammation are not exacerbated.
[0114] In this study, the effects of AW on functional recovery
measured three weeks post-TBI were studied. To follow up on the
finding that Caspase-3, a keystone protein in apoptosis (Budihardjo
et al. (1999) Annu. Rev. Cell Dev. Biol. 15:269-290), is increased
at the time of withdrawal, up- or downregulation of a long-term
marker of apoptosis, p53, was measured (Harris and Levine (2005)
Oncogene 24:2899-2908). The p53 protein alters the permeability of
mitochondrial membranes, allowing for the release of cytochrome C,
which induces the activation of apoptotic proteases, including
caspase-3 (Mattson (2003) Neuromolecular Med. 3:65-94). Also, to
determine if neuroprotection is enhanced by TW, HSP70 and BDNF were
measured, as well as necrotic lesion cavity size and reactive
gliosis. Both BDNF and HSP70 act to promote synaptic plasticity and
the release of trophic factors (Binder and Scharfman (2004) Growth
Factors 22:123-131; Feinstein et al. (1996) J. Biol. Chem.
271:17724-17732), while a reduction in necrotic lesion size
indicates protection and sparing of neuronal cells. Furthermore,
past studies have shown that progesterone plays a part in the
reduction of reactive astrocytes associated with cerebral edema and
inflammation (Djebaili et al. (2005) J. Neurotrauma 22:106-118);
this benefit may also be enhanced with tapered withdrawal.
[0115] Given the widespread effects of acute withdrawal previously
noted at the peak of withdrawal, it was predicted that these
effects would manifest themselves in long-term behavioral testing
after the initial cascade of secondary injury has subsided.
Accordingly, locomotor activity and somatosensory neglect were
assayed for subject groups undergoing TW versus AW, from one to
three weeks after injury.
Materials and Methods
[0116] Subjects. 60 male Sprague-Dawley rats weighing 290-310 g at
the time of injury were used in this experiment. Food and water
were provided ad libidum before and after surgery. Animals were
handled and weighed daily from their arrival, seven days
pre-surgery, to brain extraction three weeks post-surgery. Animals
were handled in squads of 12, with n=10 per experimental condition.
All animal procedures were approved by the Emory University Animal
Care and Use Committee, Protocol #131-2002.
[0117] Surgery. Isofluorane anesthesia was induced for four minutes
and 45 seconds at 5% and maintained at 2.5%. Normal body
temperature was maintained with a surgical heating pad placed
beneath the sterile dressings. The scalp incision area was shaved
and sterilized with iodine and isopropanol. A midline incision was
made along the scalp and the fascia cleared to expose the surface
of the skull. Medial, lateral, and dorsal stereotaxic coordinates
were determined at bregma, and a 5-7 mm diameter bilateral
craniotomy was performed mid-sagitally, 3 mm anterior to bregma.
Medial frontal cortex MFC) injury was created with a pneumatic
cortical contusion device (5 mm diameter) at a pressure of 1.7 psi,
over 50 ms with a velocity of 2.25 m/s and to a depth of 2.5 mm.
Sutures were used to close the incision after bleeding ceased.
Animals were placed in individual heated, clean recovery cages
until they awakened, and were returned to clean individual home
cages with accessible moistened food pellets. Sham animals were
anesthetized, and an incision was made at the top of the head. The
fascia was cleared to expose bregma, then the incision was sutured
closed. Sham surgeries were matched to lesion surgeries for all
experimental conditions.
[0118] Progesterone Treatment. Sham (S) and lesion (L) animals were
randomly assigned to one of three treatment groups: vehicle (VS,
VL), acute withdrawal (AWS, AWL), and tapered withdrawal (TWS,
TWL). Sixteen mg/kg progesterone treatments were dissolved in 22.5%
2-hydroxypropyl-.beta.-cyclodextrin (HBC) and administered as shown
in Table 2. Tapering was induced as halved dosages over the last
two days of treatment. Dilutions for TW treatments were made with
HBC stock. All injections were administered intraperitoneally at
one hour post-injury, and subcutaneously at six hours post-injury
and every 24 hours through the end of the treatment cycle. Five
sets of 12 animals each were used, for a total n=10 for each
experimental group over the entire experiment. Of these animals,
all were used to acquire behavioral data, four samples were used
for protein analysis, and six samples were used for histological
analysis for each test condition.
TABLE-US-00002 TABLE 2 Post-Surgery Progesterone Treatment Schedule
Progesterone Administration Days 1-5 Day 6 Day 7 AW 16 mg/kg P 16
mg/kg P 16 mg/kg P TW 16 mg/kg P 8 mg/kg P 4 mg/kg P V 22.5% HBC
22.5% HBC 22.5% HBC
[0119] Digiscan Locomoter Activity Boxes. Random order, blinded
testing occurred under red light in a quiet environment one day
before injury, and one and seven days post-withdrawal. Up to four
animals were tested using the Digiscan Activity Monitoring System
(AccuScan Instruments, Inc. Columbus, Ohio) in each trial, with a
total of three trials per test day. Rats were placed in the
furthest left corner of the Digiscan Activity Box. At that time,
the toggle switch was flipped to `on`. At exactly five minutes the
computer ceased testing, assuring that all tests were the same
length regardless of start time. Files were saved according to date
and trial number, and the number of fecal boli recorded. Activity
boxes were cleaned with 70% ethanol and dried between trials.
Center time was defined by the computer as the amount of time the
animal spent exploring the activity box away from the corners.
[0120] Somatosensory Neglect of the Forepaws. Random order, blinded
testing occurred under red light in a quiet environment at one and
seven days post-withdrawal, one hour after locomoter activity
testing. 1.3 cm diameter circular labels were placed on the left
forepaw and the rat placed in the clear plexiglass testing box. The
latency required for each rat to remove the sticker with its mouth
was recorded, with maximum test duration of two minutes. Each
animal was tested three times, with a rest period of two minutes
between trials. The testing box was cleaned with 70% ethanol and
dried between trials.
[0121] Tissue Preparation. All animals were decapitated following a
lethal 1 mL injection of Nembutal at three weeks post-injury.
Brains for histological analysis were extracted after transcardial
perfusion with 4% paraformaldehyde. After 24 hours of post-fixation
in 4% paraformaldehyde, followed by 10% sucrose and then 20%
sucrose solution in DI water, brains were mounted and frozen under
dry ice. The forebrain was cut into 25 um sections on a cryostat
and stored at -80.degree. C. on 1% gelatin-coated slides. Evenly
spaced sections 75 .mu.n apart were washed in a graded alcohol
series, 100% and 95% alcohol (2.times.5 min each) and 70% alcohol
(1.times.5 min) and stained with thionin (1 g thionin, 1.2 g sodium
acetate, 0.4 mL glacial acetic acid in 300 mL DI H20) for lesion
reconstruction. Thionin-stained sections from 4.2-2.2 mm anterior
to bregma were identified and analyzed for lesion area using Kodak
ID software. Total brain area was determined by determined by
normalizing to the volume of sham brain sections.
[0122] Brains for protein analysis were sectioned into the
immediate area of the lesion and snap frozen in 2-methyl-butane
chilled on dry ice. Samples were stored at -80.degree. C. Brain
sections were weighed to assure consistency and homogenized via a
glass Dounce in 800 mL Tper homogenization buffer (78510, Pierce,
Rockford, Ill.) with 10 .mu.l/ml of protease inhibitor cocktail
(P8340, Sigma, St. Louis, Mo.). Homogenized tissue samples were
stored at -20.degree. C. BCA and Coomassie protein assays (23235,
Pierce) were performed in triplicate at three dilutions on each
sample to determine protein concentration. The amount of brain
homogenate needed to standardize samples to 2 .mu.g/.mu.L for
Western blotting was calculated from the results of these
assays.
[0123] Immunohistochemistry. Sections used for GFAP
immunofluorescence staining were rinsed in PBS, then incubated in
0.2% TritonX in PBS for 5-10 minutes and rinsed again. Sections
were then incubated in 1.0% Bovine Serum Albumin (BSA) in PBS for
30 minutes, and left overnight at 4.degree. C. under 1:2000 GFAP
(MAB3402, Chemricon) in 1% BSA. After a rinse in PBS and a ten
minute incubation in 1% BSA, sections were incubated in 1:1000
mouse-conjugated AlexaFluor 594 (A21125, Invitrogen, Carlsbad,
Calif.) secondary antibody solution in 1% BSA overnight at
4.degree. C. Slides were cover slipped using Vectashield Mounting
Medium (H-1000, Vector Laboratories, Burlingame, Calif.). Slides
were processed at 40.times. magnification with a Nikon Olympus
microscope equipped with epifluorescence. Prior to acquiring and
analyzing images, the microscope was calibrated to 1 .mu.m. Four
separate areas directly adjacent to the injury area were analyzed
per section. Luminosity was quantified for n--6 per treatment group
with Adobe Photoshop v. 6.0. For each 144k+pixel image, the rating
is determined and averaged per pixel over the whole.
[0124] Western Blotting. Reducing sample buffer was prepared as
0.625 M Tris, 10% Glycerol, 2% SDS, 5% .beta.-mercaptoethanol and
0.001% Bromophenol Blue. Samples were set to 2 .mu.g/.mu.l protein
concentration. Prepared samples were applied to 4-20% gradient
TrisHCL gels (345-0033, Biorad, Hercules, Calif.), and run at 200
mV for approximately one hour. Proteins were then transferred onto
PVDF membranes in the Criterion Western transfer module (165-6001,
BioRad), blocked for several hours in milk protein diluent
(50-82-00, KPL, Gaithersburg, Md.) and then incubated in primary
antibody overnight at 4.degree. C., including p53 (SC-1312, Santa
Cruz Biotechnology, Santa Cruz, Calif.) BDNF (AB 1534, Chemicon,
Temecula, Calif.) and HSP70 (33-3800, Zymed, Carlsbad, Calif.).
HRP-conjugated secondary antibodies (4-18-18, 14-13-06, KPL) were
applied the following day for 2 hours and shaken at room
temperature. Blots were developed with SuperSignal West Dura
substrate (34076, Pierce) using a Kodak scanner and Kodak ID
software for densitometry analysis. Loading controls were performed
with .beta.-actin housekeepers.
[0125] Statistics. All results were expressed as the mean plus or
minus the standard error of the mean. Statistical significance was
set at p<0.05 for two-tailed tests, and data were analyzed using
one-way analysis of variance (ANOVA) followed by LSD post hoc
tests. F-values are presented as a preface to post-hoc analysis
with all 5 degrees of freedom for Western blotting at (5,18) and
for behavior at (5,26). LSD results were used to demonstrate
significance.
Results
[0126] Behavioral Assays. Somatosensory neglect data is shown at
one day (FIG. 3A) and one week (FIG. 3B) post-withdrawal. At both
time points, TWS and VS showed no differences. At one day post
withdrawal, AWS demonstrated elevated sensory deficiencies compared
to the TWS and VS groups (*, p<0.05, F=8.97), however, at one
week post withdrawal these differences were no longer evident. At
both time points, AWL and VL did not display differences, however,
both decrease from one to seven days. TWL, however, remained the
same over the course of the experiment, and deficiencies were
decreased compared to VL and AWL (#, p<0.05, F 10.71, 8.85) at
both times.
[0127] Center time, as determined from Digiscan Locomoter Activity
Boxes, followed a similar pattern to that seen in the progression
of sensory neglect between one (FIG. 4A) and seven (FIG. 4B) days
post-withdrawal. At one day, AWS animals demonstrated significantly
less center time compared to other shams (*, p<0.05, F=6.79); at
seven days all sham animals spent equivalent center time. TWS
animals did have increased center time at one day compared to VS
animals (#, p<0.05, F=10.13). This indicated an anxiogenic
effect of progesterone withdrawal beyond the peak of withdrawal. At
both time points, TWL animals demonstrated increased center time
over AWL animals (**, p<0.05, F=7.74, 5.33), which in turn had
increased center time compared to VL animals (##, p<0.05,
F=8.91, 10.77).
[0128] Protein Analysis. FIG. 5 shows p53, a long-term marker of
apoptosis. At two weeks post-withdrawal, all progesterone-treated
animals had p53 levels indistinguishable from vehicle shams. VL
animals, however, had significantly higher p53 levels than all
other groups (*, p<0.05, F=8.67). HSP70, a neuroprotective
protein, was increased in TWL animals (*, p<0.05, F=26.94) over
both VL and AWL (FIG. 6). Sham animals did not display any
differences between treatment groups.
[0129] FIG. 7 demonstrates an increase in BDNF levels for TWL over
AWL (*, p<0.05, F=6.88) and AWL over VL (#, p<0.05, F=6.57).
Sham animals did not display any differences between treatment
groups. Coupled with HSP70 data, this indicates that the
neuroprotective properties of progesterone are enhanced with a
tapered treatment regime.
[0130] Histology. Lesion reconstruction was performed at +2.2,
+3.2, and +4.2 mm from bregma. The ratio of lesion volume to total
volume was determined for an n=4 for each depth. FIG. 8A shows
representative images of the selected sections anterior to bregma,
and the quantified data for each lesion group is shown in FIG. 8B.
TWL brains had a smaller lesion volume than AWL and VL animals (*,
#, p<0.05, F=7.32), while AWL lesion volume was decreased
compared to VL animals (*, p<0.05, F=4.55).
[0131] FIG. 9 demonstrates relative reactive astrocytes as
determined by immunofluorescent GFAP staining at three weeks
post-injury. FIG. 9A shows representative views from each group at
the lesion site or the corresponding tissue in sham animals while
FIG. 9B shows the quantified luminosity averaged over n=6. GFAP was
upregulated in VL (A) animals over AWL (B) animals, and in AWL
compared to TWL (C) animals (*, p<0.05, F=16.24, 27.96). AWS (E)
animals had an increase in GFAP reactivity over both VS (D) and TWS
(F) groups (#, p<0.05, F=9.71). TWS and VS groups did not
display differences.
Discussion
[0132] This study investigated the effects of acute progesterone
withdrawal three weeks after injury, and found selective long-term
repercussions. Several measures of long-term behavioral,
anatomical, and molecular functions were investigated to indicate
recovery of activity, sensory and cellular response.
[0133] In order to determine long-term behavioral responses to
acute versus tapered progesterone withdrawal, locomotor activity
and somatosensory neglect tests were performed. Animals with
tapered withdrawal from progesterone performed better one day and
one week post-withdrawal for both sensory recovery of function and
locomotor activity. Additionally, at one day post-withdrawal,
sham-operated animals that underwent acute progesterone withdrawal
demonstrated more deficiencies in these assays than tapered or
vehicle sham animals; this effect disappeared one week later. An
interesting observation immediately post-withdrawal was an increase
in the time spent in the center of the activity box for tapered
shams over vehicle shams. This increased exploratory behavior may
be due to a mild excitatory effect from the gradual withdrawal, in
contrast to the more severe excitotoxic, and limiting effect of the
acute withdrawal. In addition, mild excitation may further enhance
long term recovery of function, as delayed exercise after TBI
improves function recovery (Griesbach et al. (2004) Neuroscience,
125:129-139; Kleim et al. (2003) Neurochem. Res., 28:1757-1769;
Will et al. (2004) Prog. Neurobiol., 72:167-182).
[0134] Selective effects of acute versus tapered PW were also seen
in terms of molecular analyses three weeks after injury. While
apoptosis was increased for acute compared to tapered PW at the
time of withdrawal (Cutler et al. (2005) Exp. Neurol.,
195:423-429), this effect was no longer evident two weeks later as
determined by p53 protein levels. Vehicle-treated animals, however,
did maintain elevated apoptosis compared to progesterone
treatments.
[0135] A greater long-term consequence of acute withdrawal was seen
in terms of neuroprotection. BDNF and HSP 70, both indicators of
neuroprotection, were increased for tapered compared to acute
withdrawal, while all progesterone treatment resulted in increased
HSP70 compared to vehicle-treated animals. Specifically, BDNF acts
to protect tissue from insult and enable post-trauma neuronal
plasticity through various mechanisms (Binder and Scharfman (2004)
Growth Factors, 22:123-131; Chuang (2004) Crit. Rev. Neurobiol.,
16:83-90; Gonzalez et al. (2004) Neuroscience, 125:605-614), while
HSP 70 acts as a neuroprotective agent by suppressing inflammatory
responses and cytotoxicity (Feinstein et al. (1996) J. Biol. Chem.,
271:17724-17732). Taken together, the present molecular findings
and the decreased necrotic lesion volume for tapered over acute
progesterone over vehicle treatment, demonstrated an overall
picture of enhanced neuroprotection and neuroplasticity with
tapered progesterone administration.
[0136] Immunofluorescent staining for GFAP indicated the extent of
astrocyte reactivity adjacent to the injury site. While an increase
in GFAP can be a hallmark of increased trophic factors, it also
indicates glial scarring, inflammation, and cerebral edema (Hatten
et al. (1991) Glia, 4:233-243; Leme and Chadi (2001) Arq.
Neuropsiquiatr., 59:483-492). As predicted, in the present study an
increased response for vehicle-treated lesion animals and a
decreased GFAP reaction for acute progesterone-treated lesion
animals was observed. The GFAP response was further decreased for
tapered progesterone-treated lesion animals.
[0137] It should also be noted that an increase in the luminosity
of GFAP immunofluorescence was found in the acute PW sham group.
Without being bound by theory, the mechanism of sham response may
be based solely on effects stemming from acute PW. After acute
progesterone withdrawal, increased action of the NMDA and sigma
receptors creates an environment of neural excitation. The degree
of this excitation is dependent on several factors, including
dosage and duration of administration (Rupprecht et al. (2001)
Brain Res. Brain Res. Rev., 37:59-67; Rupprecht and Holsboer (2001)
Int. Rev. Neurobiol. 46:461-477), and may also be compounded by
external events such as trauma. Accordingly, an effect of recovery
from an excitotoxic environment could be increased trophic factor
release (Acarin et al. (1999) J. Neuropathol. Exp. Neurol.,
58:389-397; Horvath et al. (2000) Eur. J. Pharmacol. 405:33-42), as
observed in acute PW sham animals.
[0138] These combined molecular and immunohistological data support
the previous findings described above (see Experiment 3; Cutler et
al. (2005) Exp. Neurol., 195(2):423-429), showing that while
progesterone can be a vital therapeutic treatment, its beneficial
effects are further enhanced by reducing the secondary
complications attributable to acute PW. The clinical implications
of these findings hold promise for designing an effective response
to both the immediate and long-term rehabilitative requirements
after TBI. In order to optimize treatment and promote all stages of
functional recovery, the current study could be applied to
encompass post-trauma rehabilitation, including the effects of
exercise and enriched environments (Griesbach et al. (2004)
Neuroscience, 125:129-139; Kempermann et al. (2000) Prog. Brain
Res., 127:35-48; Will et al. (2004) Prog. Neurobiol., 72:167-182).
Also, while young adults are the largest demographic for TBI, both
immature and elderly patients contribute significantly to TBI
statistics through shaken baby syndrome, accidents, and falls (CDC,
2004) and may also benefit from such therapeutic strategies.
[0139] In conclusion, both long and short-term indices of recovery
are enhanced with tapered progesterone treatment. This knowledge
opens the door to more effective design, research, and
implementation of a safe and effective clinical treatment for
TBI.
SUMMARY
[0140] Adult, male Sprague-Dawley rats received either bilateral
frontal cortex contusion (L) or sham (S) surgery. Rats were
injected at one and six hours post injury, then every 24 hours for
six days. Vehicle (V) treated rats were given 9 injections of 22.5%
cyclodextrin, while AW rats received 9 injections of 16 mg/kg
progesterone and TW rats received 7 injections of progesterone at
16 mg/kg, followed by one at 8 mg/kg and one at 4 mg/kg. On day 8,
sensory neglect and locomotor activity tests were initiated.
Animals were dilled 22 days post-TBI and the brains prepared for
either molecular or histological analysis. Western blotting
revealed increased BDNF and HSP 70 in TW vs. AW animals. P53 was
increased in VL animals, while all progesterone-treated groups were
equivalent to shams. TW animals had markedly decreased sensory
neglect compared to AW animals, and increased center time in
locomotor activity assays. In addition, lesion reconstruction
revealed a decreased lesion size for TWL over AWL over VL animals.
GFAP immunofluorescent staining followed this pattern as well. In
conclusion, after TBI, AW affects select behaviors and molecular
markers in the chronic recovery period.
[0141] All publications and patent applications mentioned in the
specification are indicative of the level of those skilled in the
art to which this invention pertains. All publications and patent
applications are herein incorporated by reference to the same
extent as if each individual publication or patent application was
specifically and individually indicated to be incorporated by
reference.
[0142] Although the foregoing invention has been described in some
detail by way of illustration and example for purposes of clarity
of understanding, it will be obvious that certain changes and
modifications may be practiced within the scope of the appended
claims.
* * * * *