U.S. patent application number 11/902599 was filed with the patent office on 2008-12-18 for liver protection compounds of the cyclohexenone type from antrodia camphorata.
This patent application is currently assigned to Golden Biotechnology Corporation. Invention is credited to Mao-Tien Kuo, Sheng-Yun Liu, Wu-Che Wen.
Application Number | 20080312335 11/902599 |
Document ID | / |
Family ID | 39048353 |
Filed Date | 2008-12-18 |
United States Patent
Application |
20080312335 |
Kind Code |
A1 |
Liu; Sheng-Yun ; et
al. |
December 18, 2008 |
LIVER PROTECTION COMPOUNDS OF THE CYCLOHEXENONE TYPE FROM ANTRODIA
CAMPHORATA
Abstract
The present invention relates to a compound of Antrodia
camphorata used for liver protection, in particular to an extract,
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone which is isolated from Antrodia camphorate. The
cyclohexenone compound according to the invention helps to
alleviate liver injury and fibrosis induced by chemicals and
reduces the levels of alanine aminotransferase (ALT) and aspartate
aminotransferase (AST). By increasing the contents of glutathione
peroxidase (GSHPX) and catalase (CAT), cyclohexenone further
decreases the liver damage and the oxidative pressure caused by
free radicals, enhances the antioxidant ability and achieves the
purposed of liver protection.
Inventors: |
Liu; Sheng-Yun; (Taipei
Hsien, TW) ; Wen; Wu-Che; (Taipei Hsien, TW) ;
Kuo; Mao-Tien; (Taipei Hsien, TW) |
Correspondence
Address: |
BIRCH STEWART KOLASCH & BIRCH
PO BOX 747
FALLS CHURCH
VA
22040-0747
US
|
Assignee: |
Golden Biotechnology
Corporation
|
Family ID: |
39048353 |
Appl. No.: |
11/902599 |
Filed: |
September 24, 2007 |
Current U.S.
Class: |
514/690 ;
435/183; 435/184; 568/377 |
Current CPC
Class: |
A61P 1/16 20180101; C07C
403/02 20130101; C07C 2601/16 20170501; A61K 31/12 20130101; A61K
36/07 20130101 |
Class at
Publication: |
514/690 ;
568/377; 435/184; 435/183 |
International
Class: |
A61K 31/122 20060101
A61K031/122; C07C 49/675 20060101 C07C049/675; C12N 9/99 20060101
C12N009/99; C12N 9/00 20060101 C12N009/00; A61P 1/16 20060101
A61P001/16 |
Foreign Application Data
Date |
Code |
Application Number |
Jun 14, 2007 |
TW |
096121548 |
Claims
1. A method for liver protection which comprises administering to a
subject in need thereof an effective amount of a cyclohexenone
compound of Antrodia camphorata having the following formula:
##STR00003## wherein X and Y is oxygen or sulfur, R.sub.1, R.sub.2
and R.sub.3 are each a hydrogen atom, methyl or
(CH.sub.2).sub.m-CH.sub.3, and m=1-12; n=1-12;
2. The method as claimed in claim 1, wherein the compound is
isolated from the organic solvent extracts of Antrodia
camphorata.
3. The method as claimed in claim 2, wherein the organic solvents
are selected from the group consisting of alcohols, esters,
alkanes, and halogenated alkanes.
4. The method as claimed in claim 3, wherein the alcohol is
ethanol.
5. The method as claimed in claim 1, wherein the compound is
isolated from the aqueous extracts of Antrodia camphorata.
6. The method as claimed in claim 1, wherein the compound is
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone.
7. The method according to claim 1, wherein the compound can
prevent and alleviate liver injury and fibrosis in mammals.
8. The method according to claim 6, wherein the compound can
prevent and alleviate liver injury and fibrosis in mammals.
9. The method as claimed in claim 7, wherein the amount of the
compound to be administered is in the range of 300-3000 mg/kg body
weight.
10. The method as claimed in claim 8, wherein the amount of the
compound to be administered is in the range of 300-3000 mg/kg body
weight.
11. The method as claimed in claim 7, wherein the mammal is a
human.
12. The method as claimed in claim 8, wherein the mammal is a
human.
13. The method as claimed in claim 7, wherein the liver injury is
caused by chemical compounds.
14. The method as claimed in claim 8, wherein the liver injury is
caused by chemical compounds.
15. The method as claimed in claim 13, wherein the chemical
compound is carbon tetrachloride (CCl.sub.4).
16. The method as claimed in claim 14, wherein the chemical
compound is carbon tetrachloride (CCl.sub.4).
17. The method as claimed in claim 7, wherein the compound protects
liver by inhibiting the levels of alanine aminotransferase (ALT)
and aspartate aminotransferase (AST).
18. The method as claimed in claim 8, wherein the compound protects
liver by inhibiting the levels of alanine aminotransferase (ALT)
and aspartate aminotransferase (AST).
19. The method as claimed in claim 7, wherein the compound
alleviates the liver injury induced by free radicals through
increasing the levels of glutathione peroxidase (GSHPx) and
catalase (CAT).
20. The method as claimed in claim 8, wherein the compound
alleviates the liver injury induced by free radicals through
increasing the levels of glutathione peroxidase (GSHPx) and
catalase (CAT).
21-22. (canceled)
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a liver protection
compound, in particular to a cyclohexenone compound isolated and
purified from Antrodia camphorata extracts, which can be applied in
liver protection and alleviation of liver injury and fibrosis.
[0003] 2. The Prior Arts
[0004] The liver is the largest and most complicated organ of
metabolism in the body, which is responsible for metabolizing fats,
carbohydrates, proteins, vitamins, hormones, and bile. Besides, it
has abilities of secretion, excretion, biological transformation
and the like. Liver is also an important barrier organ where the
detoxification is important to protect the organism. Damaged liver
function can cause impaired metabolism, which may affect the
function of other organs or can lead to death when serious. The
prevalence of liver diseases is quite high in Taiwan. According to
the Department of Health in Taiwan, chronic liver disease and liver
cirrhosis ranked the sixth among the top ten causes of death for
Taiwan people, and caused more than 3000 death per year. The rate
is still increasing. Therefore, development of liver protection
substances, further to prevent or treat liver related diseases, is
crucial at present.
[0005] Antrodia camphorata is also called Chang-Zhi, Niu Chang-Zhi,
red camphor mushroom and the like, which is a perennial mushroom
belonging to the order Aphyllophorales, the family Polyporaceae. It
is an endemic species in Taiwan growing on the inner rotten heart
wood wall of Cinnamomum kanehirae Hay. Cinnamoum kanehirai Hay is
rarely distributed and being overcut unlawfully, which makes
Antrodia camphorata growing inside the tree in the wild became even
rare. The price of Antrodia camphorata is very expensive due to the
extremely slow growth rate of natural Antrodia camphorata that only
grows between Junes to October.
[0006] The fruiting bodies of Antrodia camphorata are perennial,
sessile, hard and woody, which exhales strong smell of sassafras
(camphor aroma). The appearances are various with plate-like,
bell-like, hoof-like, or tower-like shapes. They are reddish in
color and flat when young, attached to the surface of wood. Then
the brims of the front end become little curled tilted and extend
to the surroundings. The color turns to be faded red-brown or cream
yellow brown, with ostioles all over. This region is of very high
medical value.
[0007] In traditional Taiwanese medicine, Antrodia camphorata is
commonly used as an antidotal, liver protective, anti-cancer drug.
Antrodia camphorata, like general edible and medicinal mushrooms,
is rich in numerous nutrients including polysaccharides (such as
.beta.-glucosan), triterpenoids, superoxide dismutase (SOD),
adenosine, proteins (immunoglobulins), vitamins (such as vitamin B,
nicotinic acid), trace elements (such as calcium, phosphorus and
germanium and so on), nucleic acid, agglutinin, amino acids,
steroids, lignins and stabilizers for blood pressure (such as
antodia acid) and the like. These physiologically active
ingredients are believed to exhibit effects such as: anti-tumor
activities, increasing immuno-modulating activities, anti-allergy,
anti-bacteria, anti-high blood pressure, decreasing blood sugar,
decreasing cholesterol, liver protection, anti-fatigue, and the
like.
[0008] Triterpenoids are the most studied component among the
numerous compositions of Antrodia camphorata. Triterpenoids are the
summary terms for natural compounds, which contain 30 carbon atoms
with the pent acyclic or hex acyclic structures. The bitter taste
of Antrodia camphorata is from the component of triterpenoids.
Three novel ergostane-type triterpenoids (antcin A, antcin B,
antcin C) were isolated by Cherng et al. from the fruiting bodies
of Antrodia camphorata (Cherng, I. H., and Chiang, H. C. 1995.
Three new triterpenoids from Antrodia cinnamomea. J. Nat. Prod.
58:365-371). Three new compounds zhankuic acid A, zhankuic acid B
and zhankuic acid were extracted from the fruiting bodies of
Antrodia camphorata with ethanol by Chen et al. (Chen, C. H., and
Yang, S. W. 1995. New steroid acids from Antrodia cinnamomea,--a
fungus parasitic on Cinnamomum micranthum. J. Nat. Prod.
58:1655-1661). In addition, Cherng et al. also found three other
new triterpenoids from the fruiting bodies of Antrodia camphorata,
which are sesquiterpene lactone and 2 biphenyl derived compounds,
4,7-dimethoxy-5-methy-1,3-benzodioxole and
2,2',5,5'-teramethoxy-3,4,3',4'-bi-methylenedioxy-6,6'-dimethylbiphenyl
(Chiang, H. C., Wu, D. P., Chemg, I. W., and Ueng, C. H. 1995. A
sesquiterpene lactone, phenyl and biphenyl compounds from Antrodia
cinnamomea. Phytochemistry. 39:613-616). In 1996, four novel
ergostane-type triterpenoids (antcins E and F and methyl antcinates
G and H) were isolated by Chemg et al. with the same analytic
methods (Chemg, I. H., Wu, D. P., and Chiang, H. C. 1996.
Triteroenoids from Antrodia cinnamomea. Phytochemistry.
41:263-267). And two ergostane related steroids, zhankuic acids D
and E together with three lanosta related triterpenes, 15
alpha-acetyl-dehydrosulphurenic acid, dehydroeburicoic acid,
dehydrosulphurenic acid were isolated by Yang et al. (Yang, S. W.,
Shen, Y. C., and Chen, C. H. 1996. Steroids and triterpenoids of
Antrodia cinnamomea--a fungus parasitic on Cinnamomum micranthum.
Phytochemistry. 41:1389-1392).
[0009] Although Antrodia camphorata extracts were reported to have
the abovementioned effects from previous experiments, and the
components were analyzed in succession, further experiments are
needed to identify the effective composition for liver protection.
The application in liver diseases treatment and prevention of
components from Antrodia camphorata extracts will be of great
beneficial effects from studies of liver protection if the real
effective composition is found.
SUMMARY OF THE INVENTION
[0010] In order to identify which are the compounds to prevent or
treat liver diseases from the extracts of Antrodia camphorata, the
compound of the formula (1) was isolated and purified in the
present invention,
##STR00001##
wherein X and Y can be oxygen or sulfur, R.sub.1, R.sub.2 and
R.sub.3 are each a hydrogen atom, methyl or
(CH.sub.2).sub.m--CH.sub.3 and m=1-12; n=1-12.
[0011] A preferred compound of the general formula (1) is
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone as shown in formula (2), with molecular formula
of C.sub.24H.sub.38O.sub.4, appearance of pale yellow powder and
molecular weight of 390.
##STR00002##
[0012] Cyclohexenone compounds having the structures of formula (1)
and formula (2) are purified from aqueous extraction or organic
solvent extraction of Antrodia camphorata. The organic solvents
used include, but not limited to, alcohols such as methanol,
ethanol or propanol, esters such as ethyl acetate, alkanes such as
hexane, or halogenated alkanes such as chloromethane, chloroethane.
Among them, alcohol is preferred, and ethanol is particularly
preferred.
[0013] Cyclohexenone compounds of formula (1) and formula (2)
according to the present invention are applied in liver protection
and alleviation of liver injury and fibrosis. Feeding cyclohexenone
to carbon tetrachloride (CCl.sub.4) treated rats helped to
alleviate the progress of rat liver injury and fibrosis. The levels
of alanine aminotransferase (ALT) and aspartate aminotransferase
(AST) were decreased to achieve liver protection ability. In
addition, cyclohexenone from Antrodia camphorata helped to increase
glutathione peroxidase (GSHPx) and antioxidant enzymes catalase
(CAT) in the liver in order to decrease the liver cell injury and
lower the oxidative pressure induced by free radicals, further to
increase antioxidant ability.
[0014] On the other hand, the compounds of formula (1) and/or
formula (2) in the present invention can be incorporated into
pharmaceutical compositions for treating liver injury to improve
the symptoms induced by liver injury in mammals such as human. The
pharmaceutical compositions include not only the compounds of
formula (1) and/or formula (2), but also the pharmaceutically
accepted carries. Examples of such carriers include, but are not
limited to, excipients such as water, fillers such as sucrose or
starch, binders such as cellulose derivatives, diluents,
disintegrants, absorption enhancers or sweeteners. The compositions
can be manufactured through mixing the compounds of formula (1)
and/or formula (2) with at least one of the carriers by means of
conventional methods known in the pharmaceutically technical field,
which can be formulated in the form of, but are not limited to,
powder, tablets, capsules, pellets, granules or other liquid
formulation.
[0015] The present invention is further explained in the following
embodiment illustration and examples. Those examples below should
not, however, be considered to limit the scope of the invention, it
is contemplated that modifications will readily occur to those
skilled in the art, which modifications will be within the spirit
of the invention and the scope of the appended claims.
[0016] The patent or application file contains at least one drawing
executed in color. Copies of this patent or patent application
publication with color drawing(s) will be provided by the office
upon request and payment of the necessary fee.
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] FIG. 1 The body weights of rats from each group. *: normal
control (gp. A); .quadrature.: model control (gp. B, animals
receiving 20% CCl.sub.4); .quadrature.: positive control (gp. C,
animals receiving 20% CCl.sub.4 and silymarin); .box-solid.:
animals receiving 20% CCl.sub.4 and 300 mg/kg cyclohexenone (gp.
D); .tangle-solidup.: animals receiving 20% CCl.sub.4 and 1000
mg/kg cyclohexenone (gp. E), and : animals receiving 20% CCl.sub.4
and 3000 mg/kg cyclohexenone (gp. F).
[0018] FIG. 2 The amounts of food intake in rats from each group. :
normal control (gp. A); .DELTA.: model control (gp. B, animals
receiving 20% CCl.sub.4); .quadrature.: positive control (gp. C,
animals receiving 20% CCl.sub.4 and silymarin); : animals receiving
20% CCl.sub.4 and 300 mg/kg cyclohexenone (gp. D);
.tangle-solidup.: animals receiving 20% CCl.sub.4 and 1000 mg/kg
cyclohexenone (gp. E), and : animals receiving 20% CCl.sub.4 and
3000 mg/kg cyclohexenone (gp. F).
[0019] FIG. 3 The pathological changes of the liver surface
observed with naked eyes in rats from each group. (A) normal
control (gp. A, corn oil only); (B) model control (gp. B, animals
receiving 20% CCl.sub.4); (C) positive control (gp. C, animals
receiving 20% CCl.sub.4 and 200 mg/kg silymarin); (D) animals
receiving 20% CCl.sub.4 and 300 mg/kg cyclohexenone (gp. D); (E)
animals receiving 20% CCl.sub.4 and 1000 mg/kg cyclohexenone (gp.
E), and (F) animals receiving 20% CCl.sub.4 and 3000 mg/kg
cyclohexenone (gp. F).
[0020] FIG. 4 The pathological changes of CCl.sub.4-induced liver
injury in rats of the invention. (A) H&E staining, magnified
200-fold; (B) H&E staining, magnified 400-fold; (C) MT staining
of collagen fibers, magnified 100-fold, showing vacuoles, fibrosis
with nodules, and formation of cirrhosis.
[0021] FIG. 5 The pathological changes of liver fibrosis in rats
before or after CCl.sub.4 induction with MT staining on collagen
fibers. (A) normal liver tissue; (B) various extents of liver
fibrosis and proliferation of collagen after CCl.sub.4 treatment;
(C) incomplete septa between central vein and periportal region
after CCl.sub.4 treatment; (D) intact septal fibrosis and bridging,
many nodules in liver, the septa is thin; (E) complete thick septa,
definite cirrhosis after CCl.sub.4 treatment; (F) liver fibrosis
and green collagen after CCl.sub.4 treatment. (A) to (E): 40-fold
magnification; (F) 100-fold magnification.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
[0022] The mycelia, fruiting bodies or mixture of both from
Antrodia camphorata are first extracted with water or organic
solvents to obtain the aqueous extract or organic solvent extract
of Antrodia camphorata using the methods well known in the arts.
The organic solvents include, but not limited to, alcohols such as
methanol; ethanol or propanol; esters such as ethyl acetate;
alkanes such as hexane; or halogenated alkanes such as
chloromethane, and chloroethane. Among them, alcohol is preferred,
and ethanol is particularly preferred.
[0023] The aqueous or organic solvent extracts of Antrodia
camphorate were subjected to high-performance liquid chromatography
(HPLC) for isolation and purification. Each fraction was recovered
and applied to liver protection assay. The potent fractions with
liver protective ability were analyzed for the composition and
further assayed with related biochemical tests for alleviating
liver injury. The above approach then led to the identification of
compounds of formula (1) and formula (2) in liver protection by
alleviating liver injury.
[0024] The compound
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone of the formula (2) is explained below as an
example for the present invention. Liver protective ability of
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone were assessed by evaluating the extent of liver
injury in liver fibrosis with analysis of the markers of liver
injury such as ALT, AST, glutathione (GSH), glutathione peroxidase
(GSHPx), catalase (CAT), superoxide dismutase (SOD) after feeding
various dosages of cyclohexenone from Antrodia camphorata on
chronic liver injury of rats induced by carbon tetrachloride.
[0025] These assays have proved that
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone from Antrodia camphorata can be used to
alleviate liver injury and fibrosis caused by chemicals. The levels
of inflammatory markers ALT and AST were decreased, the levels of
GSHPx and CAT in the liver were increased in order to decrease the
liver cell injury and lower the oxidative pressure induced by free
radicals, further to increase antioxidant ability of the liver. The
details of the examples are described as follows:
EXAMPLE 1
Isolation of
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone
[0026] One hundred grams of mycelia, fruiting bodies or mixture of
both from Antrodia camphorata were placed into a flask. A proper
amount of water and alcohol (70-100% alcohol solution) was added
into the flask and were stirred at 20-25.degree. C. for at least 1
hour. The solution was filtered through a filter and a 0.45 .mu.m
membrane and the filtrate was collected as the extract.
[0027] The filtrate of Antrodia camphorata was subjected to High
Performance Liquid chromatography (HPLC) analysis. The separation
was performed on a RP18 column, the mobile phase consisted of
methanol (A) and 0.1-0.5% acetic acid (B), with the gradient
conditions of 0-10 min in 95%.about.20% B, 10-20 min in
20%.about.10% B, 20-35 min in 10%.about.10% B, 35-40 min in
10%.about.95% B, at the flow rate of 1 ml/min. The column effluent
was monitored with a UV-visible detector.
[0028] The fractions collected at 25-30 min were collected and
concentrated to yield
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone, a product of pale yellow powder. The analysis
of
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone showed the molecular formula of
C.sub.24H.sub.38O.sub.4, molecular weight of 390, melting point of
48.degree. C..about.52.degree. C. Investigation of NMR spectra
showed that .sup.1H-NMR(CDCl.sub.3) .delta. (ppm)=1.51, 1.67, 1.71,
1.75, 1.94, 2.03, 2.07, 2.22, 2.25, 3.68, 4.05, 5.07, and 5.14;
.sup.13C-NMR(CDCl.sub.3) .delta. (ppm)=12.31, 16.1, 16.12, 17.67,
25.67, 26.44, 26.74, 27.00, 39.71, 39.81, 4.027, 43.34, 59.22,
60.59, 120.97, 123.84, 124.30, 131.32, 135.35, 135.92, 138.05,
160.45, and 197.12.
EXAMPLE 2
[0029] Liver Protection Tests with Cyclohexenone of Antrodia
camphorata
[0030] The main causes for liver disease include virus, alcohol and
chemicals. Chemical induced liver injury in rats exhibits
consistent features in pathological section of human liver injury.
The liver protection assessment in this study is focused on
chemical induced liver injury. The effects of cyclohexenone from
Antrodia camphorata on chronic liver injury of rats were evaluated
through the biochemical assays of liver injury and the liver tissue
section based on the chronic liver injury model of rats induced by
carbon tetrachloride. Carbon tetrachloride (CCl.sub.4) causes
hepatocellular necrosis, further to fibrosis and cirrhosis if not
be withdrawn. The toxicity of carbon tetrachloride is activated in
the liver by the cytochrome P-450 system. The initial metabolite is
the trichloromethyl radical (.CCl.sub.3), which binds with protein
to inhibit the protein synthesis, induces imbalanced lipid
metabolism with the outcome of triglyceride accumulation. The
peroxyl product of .CCl.sub.3 induced a lipid peroxidation and
damages of cell membrane in the liver, which causes liver enzyme
secretion and cell necrosis. As cited above, the animal model of
liver injury induced by carbon tetrachloride has similarity to
human liver cirrhosis. Therefore, the model can be applied in
evaluation of the therapy effects of drugs or food compositions.
The details of the procedures are described below.
(1) Establishment of Liver Injury Animal Model Induced by
CCl.sub.4
[0031] The animal model was performed with five-week-old
Sprague-Dawley (SD) rats purchased from BioLasco Taiwan Co., Ltd.
Healthy rats weighing 220-270 g were chosen for experiment after
observing for 2 weeks in the laboratory animal room. The rats were
randomly divided into 6 groups (12 rats/group): normal (gp. A);
control groups including model control (gp. B) and positive control
(gp. C, animals receiving silymarin); treatment groups including
animals receiving 300 mg/kg of cyclohexenone (gp. D), 1000 mg/kg of
cyclohexenone (gp. E), and 3000 mg/kg of cyclohexenone (gp. F), as
indicated in Table 1. Only normal group was not poisoned with
CCl.sub.4. The body weights were recorded to calculate the dosage.
Silymarin, the flavonoid extracted from milk thistle, has been
shown to help decrease the liver inflammation and promote healing.
It helps to remove toxins from liver cells by either neutralizing
the toxicity of toxic compounds or competing with the binding sites
in liver. It is a potent antioxidant, protects the liver from free
radicals. It has been widely studied for treating various types of
liver injury in animals and clinical trials. The beneficial effects
on liver protection have made silymarin a good medicine for liver
diseases and a drug in positive control group for the animal model
of liver injury.
TABLE-US-00001 TABLE 1 The experimental groups with the substances
fed and the dosages 20%(v/v) Group CCl.sub.4 cyclohexenone
silymarin A (normal) 0 0 0 Control B (model 2 ml/kg BW 0 0 groups
control) C (positive 2 ml/kg BW 0 200 mg/kg control) Treat- D 2
ml/kg BW 300 mg/kg 0 ment E 2 ml/kg BW 1000 mg/kg 0 group F 2 ml/kg
BW 3000 mg/kg 0
[0032] Rats in normal group (group A) were fed with corn oil (Sigma
chemical co.) by means of stomach tubes. Carbon tetrachloride
(Shimakyu, Osaka, Japan) was administered to groups B to F via
stomach tubes twice weekly (every Tuesday and Thursday afternoon)
for 8 weeks, at a dose of 2 ml/kg of body weight, diluted with corn
oil. Silymarin was prepared with saline in an amount of 200 mg/kg
of body weight and was fed to rats of group C via a stomach tube.
Cyclohexenone prepared from example 1 was mixed with saline, and
fed in the amounts of 300 mg/kg, 1000 mg/kg and 3000 mg/kg of body
weight to rats of group D to F via stomach tubes. The total feeding
volume was estimated in the ratio of 10 ml/kg of body weight to
groups C to F five days a week (every morning) for 8 weeks. The
body weights of rats and the amounts of food intake in rats for
each group were shown in FIG. 1 and FIG. 2, respectively.
[0033] FIG. 1 shows the body weight changes of rats during 8 weeks
of experiment in control groups and treatment groups. The weight of
rats decreased in all CCl.sub.4-treated groups except rats in
normal group after one week of experiment though the weights in the
beginning were not significantly different among groups. The body
weights of rats in model group (gp. B, 366.9 g), were remarkably
lower than those in normal group (gp. A, 448.7 g), at the 8.sup.th
week of experiment. The treatment of CCl.sub.4 resulted in
pathological changes in rats, which caused the decrease of body
weight. In addition, rats fed with silymarin (positive control, gp.
C) showed a less decrease in weights as low as 375.8 g than rats in
model control group (gp. B). The body weights did not drop sharply
when silymarin was administered. While rats fed with cyclohexenone
from Antrodia camphorata in the amount of 300 mg/kg, 1000 mg/kg,
and 3000 mg/kg showed weights of 386.6 g, 365.1 g and 355.0 g,
respectively. This represented the feeding of cyclohexenone from
Antrodia camphorata could effectively alleviate the weight decrease
situation when receiving cyclohexenone at the amount of as low as
300 mg/kg of body weight.
[0034] FIG. 2 shows the amounts of food intake during 8 weeks of
experiment in control groups and treatment groups. The food intake
increased during the first to the 5.sup.th week of experiment,
while the intake dropped and showed decreasing trends in each group
after the 5.sup.th week. Treatment of CCl.sub.4 could affect the
food intake.
(2) Effects of CCl.sub.4 to the Weights of Liver, Kidney and
Spleen
[0035] All rats were sacrificed at the end of the 8.sup.th week of
experiment. The weights of liver, kidney and spleen were recovered
and weighted and compared with the body weights to calculate the
ratios and observe the effects of cyclohexenone from Antrodia
camphorata to CCl.sub.4 treatment. All values are expressed as
mean.+-.SD, which were evaluated using One-way Analysis of
Variance. Those with significant differences were further tested
with the Least Signnificant Difference Test (LSD) or Student t-test
to compare cyclohexenone treatment groups and normal groups,
positive control and model groups. P<0.05 was selected as
criterion for statistical significance in all cases. The results
are shown in Table 2.
TABLE-US-00002 TABLE 2 The effect of cyclohexenone from Antrodia
camphorata to the weights of organs in rats after CCl.sub.4-induced
liver injury spleen kidney liver Group (%) (%) (%) A (normal) 0.16
.+-. 0.03 0.62 .+-. 0.06 2.68 .+-. 0.33 B (model control, 0.25 .+-.
0.08* 0.76 .+-. 0.11* 3.30 .+-. 0.54* 20% CCl.sub.4) C (positive
control, 0.22 .+-. 0.05* 0.71 .+-. 0.08* 3.43 .+-. 0.63* silymarin)
Treatment groups Cyclohexenone from Antrodia camphorata (mg/kg) D.
300 mg/kg 0.20 .+-. 0.05* 0.68 .+-. 0.06* 3.29 .+-. 0.35 E. 1000
mg/kg 0.22 .+-. 0.06* 0.69 .+-. 0.13 3.20 .+-. 0.47* F. 3000 mg/kg
0.30 .+-. 0.10* 0.73 .+-. 0.08* 3.65 .+-. 0.53* 1) All values were
expressed as mean .+-. SD using MS-Excels program. *P < 0.05,
showing a significant difference between normal group and other
tested groups after analyzed with Student t-test. a: P < 0.05,
showing a significant difference between model group and other
tested groups after analyzed with Student t-test.
[0036] Each of the liver, spleen, and kidney to body weight ratio
(%) from model group is significantly higher than those from the
normal group. CCl.sub.4 has shown to cause pathological changes in
these organs by increasing the weights. The increases from
silymarin treated group are less than those of model group since
silymarin has liver protective effects. On the other hand,
CCl.sub.4 treated rats fed with different amount of cyclohexenone
from Antrodia camphorata showed increase in organ to body weight
ratio, but the increases are less than those of model group when
the amount of cyclohexenone fed was 300 mg/kg or 1000 mg/kg. These
results show beneficial effect of cyclohexenone from Antrodia
camphorata in CCl.sub.4 treated rats since the organ weights were
not consistently increased.
(3) Pathological Changes of Liver Tissues
[0037] The pathological changes of the liver surface were examined
with naked eyes when the liver was taken out from rats, and then
tissue sections were made. Half of each liver lobe was stored at
-80.degree. C. for antioxidant enzyme assay to follow up. The rest
of liver tissues were fixed in 10% formalin for one week, embedded
in paraffin cut into 2 .mu.m sections, and stained with
Hematoxyline-eosin (H&E) to visualize the lipid deposition,
inflammation, cell necrosis and fibrosis, or stained with Masson's
trichromic solution to visualize extracellular matrix and collagen
fibers for liver fibrosis development. The pathological changes of
liver injury were evaluated under light microscope (Opticphot-2,
Nikon, Tokyo, Japan) after stained with the abovementioned
solution.
[0038] Assessment of pathologic score in the chronic liver damage,
the extent of inflammation, vacuolar degeneration, liver cell
necrosis and bile duct proliferation were graded
semi-quantitatively on a "0" to "4" scale (level 0=-, none, level
1=+, slight, level 2=++, mild, level 3=+++, moderate, and level
4=++++, remarkable, according to Jonker et al. (Jonker, A. M.,
Dijkhuis, F. W., Boes, A., Hardonk, M. J. and Grond J. 1992.
Immunohistochemical study of extracellular matrix in acute
galactosamine hepatitis in rats. Hepatology. 15(3):423-31).
[0039] Liver fibrosis was evaluated semiquantitatively according to
the scoring methods from Gabriele et al. (Gabriele, B. 1997.
Silymarin retards collagen accumulation in early and advanced
biliary fibrosis secondary to complete bile duct obliteration in
rats. Hepatology 26: 643-649) and Wang et al. (Wang, G. S.,
Eriksson, L. C., Xia, L., Olsson, J. and Stal, P. 1999. Dietary
iron overload inhibits carbon tetrachloride-induced promotion in
chemical hepatocarcinogenesis: effects on cell proliferation,
apoptosis, and antioxidation. J. Hepatol. 30(4):689-98.). Fibrosis
was staged on a 0-4 scale: level 0, no fibrosis, normal liver
tissue; level 1, proliferation of collagen, portal fibrosis without
septa (proliferation of radiating fiber in central vein or
periportal region); level 2, incomplete septa between central vein
and periportal region (septa without bridging); level 3, intact
septal fibrosis and bridging, many nodules in liver, the septa is
thin; and level 4, complete thick septa, definite cirrhosis. The
results are shown in FIG. 3 to FIG. 5, and Table 3.
[0040] FIG. 3 shows the pathological changes of the liver surface
observed with naked eyes from each group. In the normal group, the
liver surface was smooth (FIG. 3A); while in the CCl.sub.4-treated
model group, the liver was yellow in color, with rough, uneven and
tough surface and swelling conditions (FIG. 3B). After rats
receiving silymarin or various amounts of cyclohexenone from
Antrodia camphorata, the extents of liver pathological changes were
significantly weaker than that of model group (FIG. 3C-FIG. 3F),
though showing swelling and pathological conditions. Among them,
rats fed with cyclohexenone in the amount of 3000 mg/kg body weight
showed the slightest condition in swelling and pathological
conditions (FIG. 3F). It shows that cyclohexenone from Antrodia
camphorata can effectively improve the surface injury symptoms
induced by CCl.sub.4 in liver surfaces.
TABLE-US-00003 TABLE 3 Histological evaluation of CCl.sub.4 induced
liver injury in rats from different group Liver injury Liver
fibrosis - + ++ +++ ++++ score - + ++ +++ ++++ score Group A
(normal) 12.sup.5) -- -- -- -- 0.0 12 -- -- -- -- 0.0 B (model
control, -- -- 2 3 4 3.2* -- -- 2 3 4 3.2* 20% CCl.sub.4) C
(positive control, -- 2 1 4 3 2.8* -- 2 1 5 3 2.8* silymarin)
Treatment groups Cyclohexenone from Antrodia camphorata (mg/kg) D.
300 mg/kg -- 5 6 -- 1 1.8*.sup.a -- 6 4 1 1 1.8*.sup.a E. 1000
mg/kg -- 3 6 1 1 2.0*.sup.a 2 1 4 3 1 2.0*.sup.a F. 3000 mg/kg -- 2
6 1 2 2.3*.sup.a -- 2 4 3 2 2.5* 1) Assessment of pathologic score
in the chronic liver damage, the extent of inflammation, vacuolar
degeneration, liver cell necrosis and bile duct proliferation were
graded semi-quantitatively according to Jonker et al. 1992 on a "0"
to "4" scale (level 0 = -, none, level 1 = +, slight, level 2 = ++,
mild, level 3 = +++, moderate, and level 4 = ++++, remarkable). 2)
Chronic liver injury score in rats = counts of pathological
rats/total counts of rats. 3) Fibrosis was staged according to
Gabriele et al. (1997) and Wang et al. (1999) on a 0-4 scale: level
0, no fibrosis, normal liver tissue; level 1, proliferation of
collagen, portal fibrosis without septa (proliferation of radiating
fiber in central vein or periportal region); level 2, incomplete
septa between central vein and periportal region (septa without
bridging); level 3, intact septal fibrosis and bridging, many
nodules in liver, the septa is thin; and level 4, complete thick
septa, definite cirrhosis. 4) Liver fibrosis score in rats = counts
of pathological rats/total counts of rats. .sup.5)Counts of
pathological rats. *P < 0.05, showing a significant difference
between normal group and other tested groups after analyzed with
Student t-test. .sup.aP < 0.05, showing a significant difference
between model group and other tested groups after analyzed with
Student t-test.
[0041] Referring to FIG. 4 and Table 3, FIG. 4 shows the
pathological changes of liver injury induced by CCl.sub.4. The
liver was swollen in tissue sections, with abundant mitotic
division and increased numbers of Kuffer cells (FIG. 4A and FIG.
4B). Vacuoles appeared, many nodules were found, and resulted in
liver cirrhosis in serious conditions (FIG. 4C). The liver of the
model group showed obvious and the most serious liver injury
condition, mainly in moderate to remarkable levels with a score of
3.2 according to Jonker et al. (Table 4). Silymarin on CCl.sub.4
induced liver injury had a score of 2.8, while the extents of liver
injury in all treatment groups fed with various amounts of
cyclohexenone from Antrodia camphorata were improved. The
remarkable effects were shown in dosages of 300 mg/kg and 1000
mg/kg, mainly distributed in slight to moderate levels with scores
of 1.8 and 2.0, respectively.
[0042] Referring to FIG. 5 and Table 3, FIG. 5 shows the
pathological changes of CCl.sub.4-induced liver fibrosis in rats.
Normal liver shows no fibrosis, and belongs to level 0 according to
Gabriele et al. (1997) and Wang et al. (1999) (FIG. 5A); while
various fibrosis levels were shown after CCl.sub.4 induction: level
1, proliferation of collagen, portal fibrosis without septa
(proliferation of radiating fiber in central vein or periportal
region) (FIG. 5B); level 2, incomplete septa between central vein
and periportal region (septa without bridging) (FIG. 5C); level 3,
intact septal fibrosis and bridging, many nodules in liver, the
septa is thin (FIG. 5D); and level 4, complete thick septa,
definite cirrhosis (FIG. 5E). The collagen in liver appeared to be
green after Masson's trichromc staining (FIG. 5F). The liver of the
model group showed the most serious liver fibrosis condition,
mainly in level 3 and level 4 with a score of 3.2 (Table 3).
Silymarin on CCl.sub.4 induced liver fibrosis had a score of 2.8,
while the extents of liver fibrosis in all treatment groups fed
with various amounts of cyclohexenone from Antrodia camphorata were
improved. The remarkable effect was shown on the dosage of 300
mg/kg, mainly distributed in level 1 to level 2 with a score of
1.8.
[0043] These results show beneficial effects of cyclohexenone from
Antrodia camphorata in CCl.sub.4 treated rats in liver injury and
liver fibrosis. CCl.sub.4 treated rats fed with different amount of
cyclohexenone from Antrodia camphorata all showed better effects
than silymarin. And the best effect was found on the dosage of 300
mg/kg.
(4) Indicators of Liver Function
[0044] Alanine aminotransferase (ALT) and aspartate
aminotransferase (AST) are important enzymes in amino acid
synthesis for human organs such as liver, heart, muscle and the
like. These enzymes maintain low contents in serum under normal
condition with levels of 40 U/L for ALT and 50 U/L for AST. The
increase in serum ALT and AST release are associated with
inflammation of cells from the abovementioned organs, which are
caused by the change of cell permeability or cell rupture.
Therefore the levels of ALT and AST are good indicators for liver
inflammation and liver injury.
[0045] All rats were sacrificed at the end of the 8th week of
experiment, blood samples were collected from abdominal aorta for
assessing liver biochemical parameters. Five ml of blood were
transferred to a tube and centrifuged at 775.times.g for 15 min.
0.5 ml of serum was analyzed on an Express plus automatic clinical
chemistry analyzer (Chiron diagnostics corporation, OH, USA) with
commercial kits of ALT (Bayer diagnostics, Cat No. E36941), AST
(Bayer diagnostics, Cat No. E37041) and cholesterol (Bayer
diagnostics, Cat No. E33940). All values are expressed as
mean.+-.SD, which were evaluated using One-way Analysis of
Variance. Those with significant differences were further tested
with the Least Signnificant Difference Test (LSD) or Student t-test
to compare cyclohexenone treatment groups and normal groups,
positive control and model groups. P<0.05 was selected as
criterion for statistical significance in all cases. The results
are shown in Table 4.
TABLE-US-00004 TABLE 4 Indicators of liver function of CCl4 induced
liver injury in rats from different group ALT AST Cholesterol Group
(U/L) (U/L) (mg/dL) A (normal) 50.7 .+-. 9.11) 110.9 .+-. 25.1 63.8
.+-. 12.2 B (model control, 453.4 .+-. 201.8* 470.4 .+-. 310.1*
66.7 .+-. 8.7 20% CCl.sub.4) C (positive control, 180.8 .+-. 94.6*
a 249.5 .+-. 105.0* a 69.5 .+-. 14.3 Silymarin) Treatment groups
Cyclohexenone from Antrodia camphorata (mg/kg) D. 300 mg/kg 226.6
.+-. 138.7* a 323.4 .+-. 189.0* 63.7 .+-. 15.1 E. 1000 mg/kg 181.7
.+-. 78.4* a 283.2 .+-. 144.2* 69.6 .+-. 14.8 F. 3000 mg/kg 206.0
.+-. 98.4* a 311.7 .+-. 99.6* 62.1 .+-. 16.2 1)All values were
expressed as mean .+-. SD using MS-Excels program. *P < 0.05,
showing a significant difference between normal group and other
tested groups after analyzed with Student t-test. a: P < 0.05,
showing a significant difference between model group and other
tested groups after analyzed with Student t-test.
[0046] The levels of ALT, AST and cholesterol in the
CCl.sub.4-treated model group were all higher than those in the
normal group. CCl.sub.4 has shown to cause liver injury, which led
to the increase in enzyme activities. The cholesterol level also
increased but not much. The increases in ALT, AST and cholesterol
from silymarin fed positive control group are less than those of
model group since silymarin has liver protective effects. On the
other hand, CCl.sub.4 treated rats fed with different amount of
cyclohexenone from Antrodia camphorata showed higher levels in ALT,
AST and cholesterol than those of normal group, but the increases
are all significantly less than those of model group (p<0.05).
The decreases of ALT and AST in comparison to the model group in
the 1000 mg/kg cyclohexenone treatment group were the most obvious
(ALT:181.7.+-.78.4 U/L, and AST:283.2.+-.144.2 U/L). These results
show that 300 mg/kg, 1000 mg/kg and 3000 mg/kg cyclohexenone from
Antrodia camphorata can effectively decrease the release of ALT and
AST on CCl.sub.4 treated rats.
(5) Antioxidant Enzymes in Liver
[0047] Antioxidant enzyme system including glutathione (GSH),
glutathione peroxidase (GSHPx), catalase (CAT), superoxide
dismutase (SOD) and the like plays a great role in protecting
organisms from oxidative damage and decrease oxidative stress when
free radicals increase. This experiment detected the contents of
antioxidant enzymes after CCl.sub.4 induced liver injury in rats
and evaluated the antioxidant ability of cyclohexenone from
Antrodia camphorata.
[0048] The liver stored at -80.degree. C. as described above was
immersed in PBS buffer (phosphate buffered saline solution, pH 7.4)
containing 0.16 mg/ml heparin. Red blood cells were removed from
the tissue. Liver was prepared as 1.0 g tissue/10 mL buffer
homogenates in fresh, chilled 50 mM phosphate, 1 mM EDTA (pH 6-7)
buffer using a Polytron homogenizer (setting 5, PT 10 probe,
Brinkmann Instruments, Westbury, N.Y.) for one min. The solution
was centrifuged at 10,000.times.g for 15 min at 4.degree. C.
Protein concentration was determined with a BCA protein assay kit
(Pierce, Ill., USA) at 550 nm using an enzyme linked immunosorbent
assay (ELISA) reader (MAX ELISA Reader, Quant, Bio-Tek Instrument,
Vermont, USA). Commercial kits of glutathione (GSH), glutathione
peroxidase (GSHPx), catalase (CAT), superoxide dismutase (SOD)
(Glutathione Assay Kit, Cat No. 703002; Glutathione Peroxidase
Assay Kit, Cat No. 703102; Catalase Assay Kit, Cat No. 707002;
Superoxide Dismutase Assay Kit, Cat No. 706002) were purchased from
Cayman Chemical Company (MI.USA) and assayed by reading at 405 nm,
340 nm, 540 nm and 450 nm using an ELISA reader. Deprotein step was
carried out for all the assays mention above except SOD assay.
Proteins were precipitated by mixing with equal volume of 10%
metaphosphoric acid (w/v), vortex-mixed evenly, centrifuged at
2,000.times.g for 2 min. The supernatant was removed for enzyme
assay. All values are expressed as mean.+-.SD, which were evaluated
using One-way Analysis of Variance. Those with significant
differences were further tested with the Least Signnificant
Difference Test (LSD) or Student t-test to compare cyclohexenone
treatment groups and normal groups, positive control and model
groups. P<0.05 was selected as criterion for statistical
significance in all cases. The results are shown in Table 5.
TABLE-US-00005 TABLE 5 Effects of cyclohexenone from Antrodia
camphorata on antioxidant enzymes to the CCl.sub.4 treated, liver
injury model animals GSH GSHPx Catalase SOD (uM/mg (nmol/ (U/mg
(U/mg Group protein) min/ml) protein) protein) A (normal) 31.5 .+-.
3.8.sup.1 11.4 .+-. 2.8 8.9 .+-. 1.4 0.65 .+-. 0.22 B (model 31.5
.+-. 6.5 9.9 .+-. 2.5 9.6 .+-. 1.6 0.80 .+-. 0.41 control, 20%
CCl.sub.4) C (positive 30.5 .+-. 4.1 9.6 .+-. 3.0 9.2 .+-. 1.4 0.68
.+-. 0.23 control, Silymarin) Treatment groups Cyclohexenone from
Antrodia camphorata (mg/kg) D. 300 mg/kg 30.3 .+-. 3.2 9.6 .+-. 1.7
9.1 .+-. 1.0 0.47 .+-. 0.17*.sup.a E. 1000 mg/kg 25.2 .+-.
1.8*.sup.a 11.2 .+-. 3.4 10.1 .+-. 1.4* 0.52 .+-. 0.28 F. 3000
mg/kg 26.7 .+-. 4.3*.sup.a 10.6 .+-. 3.1 9.8 .+-. 0.9 0.73 .+-.
0.23 GSH: Glutathione activity (uM/mg protein); GSHPx: glutathione
peroxidase activity (nmol/min/ml) one unit is defined as the amount
of enzyme that will cause the oxidation of 1 nmol of NADPH to
NADPH.sup.+ per minute at 25.degree. C.; Catalase and SOD: U/mg
protein .sup.1All values were expressed as mean .+-. SD using
MS-Excels program. *P < 0.05, showing a significant difference
between normal group and other tested groups after analyzed with
Student t-test. .sup.aP < 0.05, showing a significant difference
between model group and other tested groups after analyzed with
Student t-test.
[0049] Referring to Table 5, the levels of antioxidant enzymes in
the CCl.sub.4-treated model group were not significant different
from those in the normal group; the levels in silymarin fed
positive control group were also not significant different from
those either in the normal group or in the model group. Relatively,
the SOD level in group D (the 300 mg/kg cyclohexenone fed group)
were significantly lower than all other groups. The GSHPx and CAT
levels in group E (the 1000 mg/kg cyclohexenone fed group) and F
group (the 3000 mg/kg cyclohexenone fed group) were higher than
other groups. Both the GSHPx and CAT are able to decompose hydrogen
peroxide to non-toxic water to prevent the damage caused by
peroxides. Therefore cyclohexenone from Antrodia camphorata can
decrease the damage of free radicals, reduce the oxidative pressure
further to enhance the antioxidant ability by increasing the
contents of GSHPx and CAT.
[0050] In summary, the compound
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone isolated from Antrodia camphorata according to
the present invention can be used to effectively decrease the
extents of liver injury and liver fibrosis induced by chemicals.
The inflammation indicators of ALT and AST were also reduced. By
increasing the contents of GSHPx and CAT, cyclohexenone further
decreases the liver damage and the oxidative pressure caused by
free radicals, enhances the antioxidant ability and achieves the
purposed of liver protection. On the other hand, cyclohexenone from
Antrodia camphorata is a natural extract, which won't induce
uncomfortable side effects, toxicity or complications when applied
in treating liver injury or liver protection. It also contains
anti-free radical function such as anti-peroxides, which makes it
beneficial to human health by preventing liver injury when prepared
as health supplements, drinks and the like. In addition, it can be
incorporated into pharmaceutical compositions. The pharmaceutical
compositions include not only the active compound
4-hydroxy-2,3-dimethoxy-6-methyl-5(3,7,11-trimethyl-dodeca-2,6,10-trienyl-
)-cyclohex-2-enone, but also the pharmaceutically accepted carries.
Examples of such carriers include, but are not limited to,
excipients such as water, fillers such as sucrose or starch,
binders such as cellulose derivatives, diluents, disintegrants,
absorption enhancers or sweeteners. The pharmaceutical composition
can be manufactured through mixing the compound of cyclohexenone
from Antrodia camphorata with at least one of the carriers by means
of conventional methods known in the pharmaceutically technical
field, which can be formulated in the forms of powder, tablets,
capsules, pellets, granules or other liquid formulation, but are
not limited to. The purpose for prevention and treatment of liver
injury and liver protection can then be accomplished.
* * * * *