|
Wang-Xian
Tang, Zi-Li Dan, Guo Zhang, Mei Liu, Qin Li, Shao-Bai Li, Institute
of Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong
University of Science and Technology, Wuhan 430030, Hubei Province,
China
Hong-Mei Yan, The 7th Hospital of Wuhan, Wuhan 430071, Hubei
Province, China
Cui-Huan Wu, Department of Pathology, Tongji Medical College,
Huazhong University of Science and Technology, Wuhan 430030, Hubei
Province, China
Supported by the Natural Science Foundation of Hubei Province, No.
1999 J151
Correspondence to: Professor Wang-Xian Tang, Institute of
Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong
University of Science and Technology, Wuhan 430030, Hubei Province,
China. tangwx@tjh.tjmu.edu.cn
Telephone: +86-27-83662873
Fax: +86-27-83615970
Received: 2002-11-06
Accepted: 2003-02-11
Abstract
AIM: To observe the effects of Ganyanping on CCl4-induced
hepatic fibrosis in rats.
METHODS:
The rats were separated randomly into five groups. Groups A to group
D, each consisting of 15 rats, were for different tests, while 8
rats were used as normal controls (N). For group D, CCl4
was injected subcutaneously, at a dosage of 3 ml/kg for 9 weeks. For
group A, Ganyanping was administered via gastric tube at a dosage of
10 ml/kg. For group B, the treatment with Ganyanping was started 4
weeks after CCl4 administration. In group C, Ganyanping
was administered 8 weeks after the intoxication, and treatment
lasted for 4 weeks. Liver tissues were fixed in 10 % formalin and
embedded in paraffin. Pathologic changes, particularly fibrosis,
were evaluated on the HE and V-G-stained sections. Ten middle-power
fields were randomly selected for assessment of collagen deposition.
RESULTS:
Loss of normal hepatic architecture, some with pseudo-lobule
formation, was observed in group D, while hepatocytes steatosis and
fibrosis were less pronounced in the animals treated with Ganyanping.
Pseudo-lobule formation was not evident in the latter groups. The
total collagen area and ratio were 840.23±81.65 and 7.0±0.9,
respectively in group D, the ratio being reduced greatly in the
Ganyanping-treated groups (148.73±45.89 and
1.16±0.33,
respectively). The activities of MAO and ACP were elevated and that
of SDH in group D decreased in the hepatic tissue as compared to the
control group. The treatment with Ganyanping abrogated these
enzymatic changes.
CONCLUSION:
Our data approved that Ganyanping could improve the microcirculation
in the liver, reduce oxygen-derived free radicals, and enhance the
cellular metabolism and immune function, all resulting in an anti-fibrotic
effect. Hence, Ganyanping can protect the liver from fibrosis. It
may be a safe and effective preparation for patient with fibrosis.
Tang
WX, Dan ZL, Yan HM, Wu CH, Zhang G, Liu M, Li Q, Li SB. Experimental
study of effect of Ganyanping on fibrosis in rat livers. World J
Gastroenterol 2003;
9(6): 1292-1295
http://www.wjgnet.com/1007-9327/9/1292.asp
INTRODUCTION
Ganyanping, a preparation of Chinese herbs proposed by Li
Shaobai et al[1] has been used in clinical and
experimental fields for many years. It has been shown to be
protective for the animal liver against injury by D-GalN and
cirrhosis caused by CCl4 intoxication[2-6]. In
this study, the effects of Ganyanping on liver fibrosis used a CCl4-
intoxication model. The V-G and enzyme histochemistry techniques
were employed to observe the effects of Ganyanping.
MATERIALS
AND METHODS
Reagents
CCl4 (Beijing Chemical Factory, Lot No. 20000225) was
diluted to 40 % in vegetable oil (Southseas Oils & Fats
Industrial (CHI Wan) Limited, Grade One, Lot No. KO'SOF
Ts88). Ganyanping tablet preparation (Lot No.20001110) was provided
by the Institute of Liver Disease, Tongji Hospital, Tongji Medical
College, consisting of Radix Astragali seu Hedysari, Radix Salviae
Miltiorrhizae, Rhizoma polygoni Cuspidati and other herbs. The
tablets were prepared in the Chinese Medicine Pharmacy of Tongji
Hospital. The powder of Ganyanping was dissolved into water (1.2
g/ml) before use.
Animals
68 Wistar rats (♀ & ♂, 38 for ♀ and 30 for ♂), weighing
between 170 and 250 g, were provided by the Laboratory Animal Center
of Tongji Medical College. The rats were separated randomly into
five groups. Group N, normal control, consisted of 8 rats. For group
A to group D, rats (15 for each) were treated with CCl4
by subcutaneous injection at a dosage of 3 ml/kg for 9 weeks. For
group A, Ganyanping (10 ml/kg) was also administered via gastric
tube along with the CCl4 intoxication. For group B,
Ganyanping treatment was started 4 weeks later and lasted for the
remaining 5 weeks. For group C, Ganyanping was given after 8 weeks
of CCl4 administration, and the treatment lasted for 4
weeks. Ganyanping was administrated in the form of an aqueous
suspension (2 g/ml). After 9 weeks, the overnight fasting animals
were anesthetized with sodium pentobarbital (30 mg/kg, per
injection). Blood was taken from inferior vena cava for the
estimation of biochemical parameters including values of ALT, AST,
and concentrations of protein and albumin.
Pathological
observations
Hepatic tissues were fixed with formalin and embedded with
paraffin. The sections were stained with hematoxylin and eosin.
Samples for electron microscopy were fixed in 25 g/L glutaraldehyde
buffer for two hours, then with osmium acid, dehydrated in acetone,
and embedded with epoxy resin. The sections were observed under an
electron microscope (OPTON EM10C, Carl Zelss Company, Made
in Germany, No.5166, voltage is 60KV).
V-G
staining and enzymatic reactions
Van Gieson's method
was used to demonstrate collagen fibers[7]. HPIAS-1000
auto medical image analyzing system was used for quantitative
assessment of collagen fibers in liver. Ten middle power fields were
selected randomly for the total area occupied by collagen fibers and
its ratio against the total area observed. Activity of monoamine
oxidase (MAO) was demonstrated using 15 mm-thick frozen sections with the chayen method,
that of succinic dehydrogenase (SDH) was visualized using lojda
method, that of ALP with culling method, and that of ACP with
Bancroft method[8]. NOS was shown using NADPH method[9].
Statistics
Statistical analysis with ANOVA: Data were presented as
.
Significant differences were determined by using ANOVA in
statistical software SPSS11.0. Results were considered significant
when P<0.05.
RESULTS
Histologic and ultrastructural findings
Liver sample from group D showed loss of normal lobular
architecture. The parenchyma showed steatosis, cellular swelling,
necrosis, and was divided into rounded nodules, separated by bands
of fibrous tissues, while in groups A, B and C, the steatosis was
not severe and the fibrosis was not so pronounced, without any
pseudo-lobule observed (Figures 1, 2). Hepatocellular degeneration
was frequently seen in the intoxicated animals under electron
microscope, characterized by marked swelling of mitochondria, loss
of rough endoplasmic reticulum structures and distention of them.
Glycogen particles were greatly reduced and more lipid droplets were
found in the cytoplasmic compartment. In some hepatocytes, nuclear
irregularity was noted, lipid droplets and some components
resembling rough endoplasmic reticulum (nuclear or pseudo-nuclear
inclusions) were also found within the nuclei. A few lipid droplets
were found in the cytoplasm in the Ganyanping-treated groups
(Figures 3, 4).
VG
staining
Fibrosis was shown in group D by VG staining, with hepatic
parenchyma separated by the rough, red-stained fibrotic septa. The
change was less pronounced in the Ganyanping-treated groups. The
total collagen-deposited area and ratio in group D, but not in the
Ganyanping-treated groups (P<0.05), were increased
compared to those in the control group (P<0.001)(Table1,
Figures 5, 6).
Table
1 Area occupied by
fibrotic septa and its ratio to the total area examined
| Groups |
n |
Area
covered by fibrotic septa (um2) |
Ratio
(%) |
| N |
8 |
35.30±13.86b |
0.32±0.18b |
| A |
15 |
200.74±33.84a |
1.63±0.45a |
| B |
15 |
148.73±45.89a |
1.16±0.33a |
| C |
15 |
158.73±40.89a |
1.12±0.28a |
| D |
15 |
840.23±81.65 |
7.00±0.90 |
aP<0.05
vs Group D, bP<0.001 vs Group D.
Figure
1 Loss of
normal lobular architecture,some had pseudo lobule formation in the
CCl4 intoxicated groups. HE×100.
Figure 2
Steatosis was not severe and fibrosis was not so pronounced,
without any pseudo -lobule formation in the Ganyanping-treated
groups. HE×100.
Figure 3
The numbers of hepatic stellate cells and collagen fibrils
increased in Disse's space
and hepatocellular degeneration were frequently seen in the CCl4
intoxicated groups.×4 000.
Figure 4
Most of hepatocytes showed basically normal ultrastructure
and a few lipid droplets were found in the cytoplasm in the
Ganyanping-treated groups. ×4 000.
Figure 5
Hepatic parenchyma separated by the rough, red-stained
fibrotic septa in the CCl4 intoxicated groups. VG×200.
Figure 6
Collagen fibrosis was less pronounced in the Ganyanping-treated
groups. VG×200.
Figure 7
Increase in the activities of MAO(+++) in the CCl4
intoxicated groups. ×75.
Figure 8
Decrease in the activities of MAO in the Ganyanping-treated
groups (++). ×75.
Enzymatical
reactions
Activities of MAO, SDH, ALP and NOS were demonstrated in
frozen sections with the procedures described above. Those for MAO
and ACP were found to be elevated and that of SDH was reduced in
group D compared to those in the control group. The changes were not
so marked in any of the Ganyanping-treated groups (Tables 2, 3;
Figures 7, 8).
Table
2 Semiquantitative
assessment of enzymatic activities in different liver samples
| Groups |
n |
MAO |
SDH |
ACP |
LDH |
NOS |
ALP |
| N |
8 |
++ |
+++ |
+ |
++ |
++ |
++ |
| A |
15 |
++ |
+++ |
++ |
+↓ |
++ |
++ |
| B |
15 |
++ |
+++ |
+ |
++ |
++ |
++ |
| C |
15 |
++ |
+++ |
+ |
++ |
++ |
++ |
| D |
15 |
+++↑ |
++↓ |
+++↑ |
+↓ |
++ |
++ |
+:
positive; ++: moderately positive; +++: strongly positive; ↑:
activity enhancement; ↓:
activity weakened.
Table
3 Quantitative
observation of the liver enzymatic activities (mean absorbance)
| Groups |
n |
MAO |
SDH |
ACP |
LDH |
| N |
8 |
0.2042±0.041a |
0.4057±0.030a |
0.1160±0.0338a |
0.1685±0.0103 |
| A |
15 |
0.3201±0.066a |
0.2917±0.045a |
0.1623±0.0246a |
0.1948±0.0319 |
| B |
15 |
0.3308±0.079a |
0.3380±0.103a |
0.2101±0.0342a |
0.1331±0.0071 |
| C |
15 |
0.1835±0.060a |
0.3939±0.0434a |
0.1884±0.0542a |
0.1757±0.0216 |
| D |
15 |
0.5022±0.149 |
0.1819±0.1049 |
0.4235±0.0727 |
0.1656±0.0145 |
aP<0.05
vs group D.
DISCUSSION
It remains a problem to prevent cirrhosis or to control its
progression in patients with a chronic liver disease[10,11].
Great efforts have been made to find safe and effective drugs.
Recent clinical and experimental observations have demonstrated that
Chinese medicines might be of some preventive and therapeutic values
against fibrosis[12-20]. Ganyanping, prepared according
to the regime of Li Shaobai et al[21], has been
used for many years for this purpose. However, its effect and
associated mechanism need further experimental evidence. For this
reason, we used CCl4 to induce liver fibrosis and
investigated herein the effects of Ganyanping on fibrosis.
Liver
fibrosis is a pathologic process associated with over production and
deposition of collagen fibers[22, 23] and other
extracellular matrix (ECM) components[24-27] resulted
from various hepatic diseases. It is considered a necessary
intermediate step between liver parenchyma injury and cirrhosis[28].
Activation of hepatic stellate cells (HSCs) has been shown to be one
of the critical steps during hepatic fibrosis[29-34]. It
is associated to a number of pathological factors, resulting in ECM
deposition and hepatic fibrosis. This was also observed in the
fibrosis caused by CCl4 intoxication, and this process
could be effectively controlled by treatment with Ganyanping. The
preparation was found to be inhibitory in the collagen production.
MAO
is used as a marker for evaluating hepatic function in cirrhosis,
its elevation indicating liver damage[35]. An increase in
MAO activity was observed in the intoxication group. Ganyanping was
found to be able to abrogate this change. Thus, Ganyanping is
considered to have some anti-cirrhotic effect. SDH is a
rate-limiting enzyme in the tricarboxylic acid cycle[36,37].
The elevation of its activities reflects more active metabolism. Our
data indicate the treatment with Ganyanping might be helpful for
liver parenchyma cells to maintain this SDH activity through the
intoxication. The treatment was also shown to be helpful for
stabilizing the lysosome membrane in chronic hepatic injury,
reflected by its interference to ACP values of the animals received
intoxication. In the present study, activity of NOS was shown to be
reduced in the CCl4-intoxicated group, but the effect was
partially abrogated by the treatment with Ganyanping, indicating
that the treatment might help the liver to recover its function
through the stress caused by CCl4 administration.
In
summary, Ganyanping was found to play some anti-fibrotic role.
According to the theory of traditional Chinese medicine, Ganyanping
may possess multiple pharmaceutical effects, such as invigorating "qi"
and activating "blood",
dispersing stagnated hepatic "qi"
and facilitating the discharge of "bile",
delivering "heat"
and "toxins",
and eliminating "dampness"
in view of its composition. Our experimental data have proved that
Ganyanping could reduce oxygen-derived free radicals, and enhance
the cellular metabolism and immune function, all resulting in an
anti-fibrotic effect. Ganyanping may be used as a safe and effective
preparation for patients with fibrosis.
REFERENCES
1
Li XG, Li SB, Wang TC, Tang WX, Du LJ, Zhang WY. Protective
Effect of Gan Yanping on Con A induced liver
injury. Zhonghua Ganzangbing Zazi
1996; 4: 243-244
2
Tang WX, Yu DX, Dan ZL, Zhang WY, Du LJ, Li SB. Study on
protective effect of Traditional Chinese herbs
(Gan Yanping) on acute liver injury
induced by D-GalN in rats. Tongji Yike Daxue Xuebao
1998; 27: 56-58
3
Tang WX, Yu DX, Dan ZL, Du LJ, Zhang WY, Li SB. An
experimental study on the effect of Gan Yanping on Collagen
Fiber in rat Chronic Liver Induced by
CCl4. Weichang Bingxue He Ganbingxue Zazhi 1998; 7: 167-169
4
Du LJ, Tang WX, Dan ZL, Zhang WY, Li SB. Protective effect of
gan yanping on CCl4 induced liver fibrosis in rats.
Shijie Huaren Xiaohua Zazhi 1998; 6:
22-23
5
Du LJ, Tang WX, Dan ZL, Zhang WY, Li SB. Study of protective
effect of GanYanping in acute liver injury model.
Tongji Yike Daxue Xuebao 1997; 26:
149-151
6
Tang WX, Du LJ, Zhang WY, Xiong XK, Zhang Y. Histochemistry
study on the protective effect of Gan Yanping from
liver injury induced by D-GalN in
rats. Zhongguo Zuzhi Huaxue He Xibao Huaxue Zazhi 1996; 5: 397-340
7
Wei HS, Li DG, Lu HM, Zhan YT, Wang ZR, Huang X, Zhang J,
Chang JL, Xu OF. Effects of AT1 receptor
antagonist, losartan, on rat hepatic
induced by CCl4. World J Gastroenterol 2000; 6: 540-545
8
Pen CN, Wang Y, Niu JZ, Weng JG, Shi SS, Shun PW, Piao YJ, Li
SG, She Y, Guo SG, Peng JY, Ge ZH, Xie JY, Xiong
XK. Histochemistry.1.Beijing: People's
Medical Publishing Company 2001:
392-528
9
Punkt K, Zaitsev S, Vwllner M, Schreiter T, Fitzl G,
Buchwalow LB. Myopathy-dependent changes in activity of ATPase
SDH and GPDH and NOS expression in
the different fibre types of hamster muscles. Acta histochem 2002;
104: 15-22
10 Zeng MD. Treatment of
liver fibrosis. Zhonghua Ganzhangbing Zazhi 2001; 9: 68-69
11
Dai WJ, Jiang HC. Advances in gene therapy of liver
cirrhosis: a review. World J Gastroenterol 2001; 7: 1-8
12 Zheng LN, Han T, Wang
BE, Ma XM, Jia JD, Qian SC, Gao YT. Effect of Bupleurum on collagen
content in hepatic
stellate cell media in vitro.
Tianjing YiKe Daxue Xuebao 2001; 7: 502-504
13
Cheng ML, Wu YY, Huang KF, Luo TY, Ding YS, Lu YY, Liu RC, Wu
J. Clinical study on the treatment of liver fibrosis
due to hepatitis B by IFN-a1
and traditional medicine preparation. World J Gastroenterol 1999; 5:
267-269
14
Liu P, Liu C, Xu LM, Xue HM, Liu CH, Zhang ZQ. Effects of
Fuzheng Huayu 319 recipe on liver fibrosis in chronic
hepatitis B. World J Gastroenterol
1998; 4: 348-353
15 Li JM. Recent
condition of traditional chinese herb on treatment of fibrosis.
Tianjing Zhongyi Xueyuan Xuebao
2002; 21: 37-38
16
Cai DY, Zhao G, Chen JC, Ye GM, Bing FH, Fan BW. Therapeutic
effect of Zijin capsule in liver fibrosis in rats.
World J Gastroenterol 1998; 4:
260-263
17
Li JC, Ding SP, Xu J. Regulating effect of Chinese herbal
medicine on the peritoneal lymphatic stomata in enhancing
ascites absorption of experimental
hepatofibrotic mice. World J Gastroenterol 2002; 8: 333-337
18
Liu P, Hu YY, Liu C, Zhu DY, Xue HM, Xu ZQ, Xu LM, Liu CH, Gu
HT, Zhang ZQ. Clinical observation of salvianolic acid
B in treatment of liver fibrosis in
chronic hepatitis B. World J Gastroenterol 2002; 8: 679-685
19
Shen BS, Wong XG, Qiao HC, Lu ZH, Han Q, Wang W, Guan HL.
Preventive effect of Sanjia Yigan granule in
hepatofibrosis in rats. Shijie Huaren
Xiaohua Zazhi 1998; 6: 386-388
20
Liu CH, Hu YY, Wang XL, Liu P, Xu LM. Effects of salvianolic
acid-A on NIH/3T3 fibroblast proliferation, collagen
synthesis and gene expression. World
J Gastroenterol 2000; 6: 361-364
21 Du LJ, Tang WX, Zhang
WY, Li SB. Effect of Gan Yanping on Cytokines in acute liver injury
induced by D-GalN in
rats. Zhongxiyi Jiehe Ganbingxue
Zazhi 1998; 8: 28-30
22 Wang AM, Wang BE, Yang
YW, Zhang B, Jiang LA, Du SC. Interstitial collagenase gene
expression in patients with
liver disease. Linchuang Gandanbing
Zazhi 2000; 16: 90-91
23
Nie QH, Cheng YQ, Xie YM, Zhou YX, Cao YZ. Inhibiting effect
of antisense oligonucleotides phosphorthioate on
gene expression of TIMP-1 in rat
liver fibrosis. World J Gastroenterol 2001; 7: 363-369
24 Wang TL, Wang BE,
Zhang HH, Liu X, Dan ZP, Zhang J, Ma H, Li XM, Li NZ. Pathology
study of the therapeutic
effect on HBV-related liver fibrosis
with herbal compound 861. Zhongguo Weichang Bingxue He Ganbingxue
Zazhi 1998; 7: 148-150
25
Wang TL, Zhang B, Jie J. Effect of anti-fibrosis compound on
collagen expression of hepatic cells in experimental
liver fibrosis of rats. World J
Gastroenterol 2000; 6: 877-880
26 George J, Rao KR, Stem
R, Chandrakasan G. Dimethylnitrosamine-induced liver injuryin rats:
the early deposition
of collagen. Toxicology 2001; 156:
129-138
27 Wang BE. Heptic
stellate cell and Fibrosis. Zhonghua Ganzhangbing Zazhi 2000; 8:
197-199
28 Wang GY, Cai WM, Wang
JQ, Weng HR, Cheng F. An experimental study of histological
quantitative method in
the diagnosis of hepatic fibrosis.
Zhonghua Ganzhangbing Zazhi 1998; 6: 201-202
29
Cheng ML, Wu J, Wang HQ, Xue LM, Tan YZ, Ping L, Li CX, Huang
NH, Yao YM, Ren LZ, Ye L, Li L, Jia ML. Effect of
Maotai liquor in inducing
metallothioneins and on hepatic stellate cells. World J
Gastroenterol 2002; 8: 520-523
30
Wei HS, Lu HM, Li DG, Zhan YT, Wang ZR, Huang X, Cheng JL, Xu
QF. The regulatory role of AT 1 receptor on
activated HSCs in hepatic
fibrogenesis: effects of RAS inhibitors on hepatic fibrosis induced
by CCl4. World J
Gastroenterol 2000; 6: 824-828
31 Zhan YT, Zhan CY, Chen
YW, Li DG. Heptic stellate cell and Fibrosis. Linchuang Gandanbing
Zazhi 2000; 16: 71-73
32 Lou Y, Dai LL, Shen
DM. Research progress of hepatic stellate cell and fibrosis.
Zhonghua Ganzhangbing Zazhi
2000; 8: 251-252
33 Liu J, Zhao FD, Jia SJ,
Han QR. The study of VG staining for liver fibrosis of chrionic
liver diseases. Jilin Yixueyuan
Xuebao 1998; 18: 21-22
34 Ma H, Wang BE, Ma XM,
Jia JD. Effect of compound 861 on rat hepatic cell collagen
synthesis and degradation in
vitro. Zhonghua Ganzhangbing Zazhi
1999; 7: 30-32
35 Wang W, Liu HL.
Significance and change of HA, LN and MAO of hepatitis B patients
serum. Bao Tou Yixue Zazhi
2001; 17: 41-42
36
Shah V, Toruner M, Haddad F, Cadelina G, Papapetropoulos A,
Choo K, Sessa WC, Groszmann RJ. Impaired
endothelial nitric oxide synthase
activity associated with enhanced caveolin binding in experimental
cirrhosis
in the rat. Gastroenterology 1999;
117: 1222-1228
37 Song BC, Yin SY, Tang
WX, Xiong XK. Study on enzyme histochemistry of experimental
cirrhosis liver. Zhongguo
Zuzhi Huaxue he Xibao Huaxue Zazhi
1999; 8: 47-50
Edited
by Su
Q
| |