Traditional Chinese Medicine Can Improve Liver Microcirculation and Reduce Portal Hypertension in Liver Cirrhosis

Xu Lieming1,5, Gu Jie2, Lu Xiong2, Zhou Yang1,5, Tian Tian2, Zhang Jie2 and Xu Hong2 1Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 2Institute of Liver Diseases, Shanghai University of TCM 3Key Laboratory of Liver and Kidney Diseases, Ministry of Education 4Key Laboratory of Traditional Chinese Medicine Clinic, Shanghai 5The Key Unit of Liver Diseases, SATCM. Shanghai, China


Introduction
Liver microcirculation means that the blood circulation is sinusoids as a center, from the end branch of portal vein and hepatic artery through sinusoids to central vein in the liver.Liver microcirculation has two characteristics.One character is there are two import systems from portal vein and hepatic artery.Another is sinusoids with unique structure.All blood vessels which diameters are less 300m are part of microcirculation system.These vessels are able to regulate the blood flow and distribution. 1nusoids are a capillary bed which is major place for regulation of blood and exchange of material in the liver.Sinusoids are constituted by microvasculature, sinusoid endothelial cells SEC , Kupffer cells KC and hepatic stellate cells HSC . 2 SEC and HSC are considered as cellular factors for regulation of sinusoids blood flow.HSC is located in perisinusoids with functions include storing Vitamin A, and controlling the diameter and blood flow of sinusoids by its pseudopods around sinusoids. 3SEC, KC and HSC all have contractility because they contain fiber, microvasculature and contractile protein. 2 The liver complex functions, which are biological synthesis, metabolism, detoxify and host defense, are tightly dependent perfect liver microcirculation. 4It is showed that failure of liver microcirculation is a general pathological alteration in chronic hepatitis and liver cirrhosis because changed construction of microvasculature, capillarization of sinusoid (the collagen is filled in perisinusoids) and compression of fibrous tissue.Generally, stenosis of sinusoid will lead to increase of resistence, decrease of blood flow rate and flow volume, and formation of portal hypertension.It is indicated that after hepatitis B virus infection, platelets were recruited to the liver, and their activation correlated with severely reduced sinusoidal microcirculation, delayed virus elimination and increased immunopathological liver cell damage. 5n normal condition, liver microcirculation is regulated by 3 ways.(1) SEC is a regulator of blood flow in the liver.The liver injury will lead to injury of SEC, reduction of fenestrae in SEC, straitens of sinusoid within accumulation of erythrocytes and formation of microthrombus.Injury and necrosis of SEC are major causes of disorder of liver microcirculation.(2) KC can also regulate the liver blood flow by its pseudopod inner of sinusoid.Actived KC may lead stenosis of sinusoid due to conglutination of leukocytes. 6(3) HSC is able to directly regulate contraction of sinusoids in normal liver.Active HSC has stronger character of contraction with increased concentration of Ca 2+ .HSC is just located in the site of sinusoid contraction.Propotional relationship has been proved between contraction of HSC and activation of HSC both in vivo and in vitro. 7,8Many chemical compounds are as inductors to induce contraction of HSC.They are included Endothelin-1 (ET-1), Angiotensin II and vasopressin.ET-1 is concerned a strongest cytokine to induce contraction of HSC.Perfusion of ET-1 through portal vein leads to contraction of sinusoids.However, the compounds of NO, CO and adrenal medullar hormone have the functions to against ET-1-stimulated contraction of HSC.Contraction of active HSC (myofibroblast cell), which locates in fibrous septum in cirrhotic liver, can change construction of hepatic lobule and lead to increase resistens of microcirculation in the liver.
Once failure of microcirculation in the liver, some symptoms and signs of patient are similar "blood stasis" in Traditional Chinese Medicine.Those are twinge in inside right flank or rib, hepatomegaly or splenomegaly, dim complexion, accompanied with spider nevi and liver palms, deep-red tongue, ecchymosis, taut or thready pulse.Some Chinese herb medicine, which is able to promote blood circulation to remove blood stasis, can prevent esophageal variceal bleeding on cirrhotic patients with portal hypertension, improve liver microcirculation and decrease portal hypertension through treating cirrhotic rats in vivo and inhibit contraction of active HSC in vitro in resent 10 years. 9 Fuzheng Huayu Capsule (FZHYC), a traditional Chinese medicine recipe, has demonstrated the effect of anti-fibrosis and reduced portal vein pressure in patients with chronic hepatitis B. 10 Fuzheng means supporting the healthy energy.Huayu means dispersing blood stasis.The recipe is composed by 6 herbs those are Dan Shen (Radix Salviae Miltiorrhizae), Chong Cao (Paecilomyces hepiali Chen & Dai), Tao Ren (Semen Persicae), Jiao Gu Lan (Gynostemma pentaphyllum), Song Hua Fen (Pinus armandii Franch) and Wu Wei Zi (Fructus Schisandrae Chinensis).FZHYC has been used in numerous studies in China and has been found to have a satisfactory prophylaxis effect on the chronic liver injury and hepatic fibrosis in rats and humans.In addition, it enhances hepatic fibrolysis. 11

The clinical research 2.1 Aims
To elucidate the role of FZHYC in the prevention of esophageal variceal bleeding on cirrhotic patients with portal hypertension.

Methods
In a multi-center randomized and placebo-controlled trial, 146 cirrhotic patients, whose age range was between 18 and 70 years old, with esophageal varices were enrolled.According to the degree of esophageal and gastric varices, patients were stratified as 2 levels: small Traditional Chinese Medicine Can Improve Liver Microcirculation and Reduce Portal Hypertension in Liver Cirrhosis 95 level, and moderate and severe level.The randomization code was generated by SAS software for each subject.For patients with small varices, the trial was double blinded.The patients were randomly assigned to 2 groups: Patients were treated with FZHYC in FZHYC group or received placebo in control group.For patients with moderate and severe varices, the trial was single blind.They were divided into 3 groups: FZHYC group in which patients were treated with FZHYC, propranolol group in which patients were treated with Propranolol and combination group in which patients received both FZHYC and propranolol.The dose of FZHYC was 15 capsules (0.3g per capsule) per day and orally administrated at 3 times.The placebo was composed of stir-fried wheat powder with an identical-appearance in the aspects of dosage, color of the contents and packaging.The clinical intervention period lasts 2 years and the follow up would stop once the end points occur.The primary end point was esophageal or gastric variceal bleeding.

In patients with small varices level
A total of 6 patients reached the primary end point of esophageal variceal bleeding: 1 of 29 patients in the Fuzheng Huayu group and 5 of 27 patients in the control group.The actuarial probability of remaining free of esophageal variceal bleeding was a significant different between 2 groups (96.3% vs. 77.01%,P=0.0422) (Fig. 1).Some patients with small varices were willing to be re-examined by endoscopy after treatment and small varices was dispared in several patients.There was a significant difference of esophageal varices degree in FZHYC group compared to the control group (P=0.014).(Tab. 1 and Fig. 2).Table 1.Difference of developing small varices in FZHYC group and in controls after 24 months Fig. 2. Alteration of small varices by endoscopy examination at pre and post treatment of FZHYC.Arrow shows the small varices in a cirrhotic patient at pre treatmtnt (left).The small varices, however, was disappeared in same patient at post treatmtnt (right).

In patients with moderate and severe varices level
5 patients in FZHYC group (n=30), 8 patients in Propranolol group (n=30) and 3 patients in the combination group (n=30) had esophageal variceal bleeding during their follow-up.
Compared to the Propranolol group (56.99%), there were significant differences in the actuarial probability of remaining free of esophageal variceal bleeding in FZHYC group (76.13%,P＝0.0131) and the combination group (87.55%,P＝0.0086).Remaining free of variceal bleeding has a higher trend in combination group, but there was no significant difference between combination group and FZHYC group (P＝0.3876)(Fig. 3).

Summary
FZHYC could effectively reduce the risk of esophageal variceal bleeding for cirrhotic patients with varices; especially the combination of the capsule and Propranolol delivered a better effect.The capsule could reduce the varices size in patients with small ones.3. Actuarial probability of remaining free of esophageal variceal bleeding in cirrhotic patients with moderate and severe varices level The patients were treated with Fuzheng Huayu Capsule in FZHYC group, Propranolol in Propranolol group, or hoth in combination group for 24 months.Actuarial probability of remaining free of esophageal variceal bleeding was higher in combination group and FZHYC group than in Propranolol group.Compared with Propranolol group, the difference was significant in combination group (P<0.01) and in FZHYC group (P<0.05).Although the probability was higher in combination group than in FZHYC group, but the difference was not significant.

Aims
To investigate effect of Fuzheng Huayu Recipe and SA-B on decreasing portal vein pressure in cirrhotic rats.

Establishment of liver cirrhosis model
The Sprague-Dawley male rats were randomly divided into model group (n=46) and normal group (n=14).The rats in model group were administrated intraperitoneally with 0.5% dimethylnitrosamine (DMN) at a dose of 2ml/kg body weight for 3 consecutive days and interval 4 days per week.The treatment was for 4 weeks.The rats in normal group were administrated intraperitoneally with physiological salin at a dose of 2ml/kg body weight for same duration.

Grouping animals and drug administration
After molding, two rats were randomly sacrificed to observe pathological changes of the liver tissue.The rats in model group were randomly more divided into 3 groups, control Follow-up (months)  n=15) and the SA-B group (n=16), once liver cirrhosis was confirmed.The rats in the FZHY group were gavaged with extractor of Fuzheng Huayu Recipe.The content of extractor equals 36.9gcrude drug per 100ml.The rats in the SA-B group were gavaged with SA-B solution (125mg per 100ml).Simultaneously, the rats in control group and normal group were gavaged with water.All dose of gavage was 1ml/100g body weight, once per day, for 3 weeks.

Measurement of portal vein pressure
The rats were anesthetized with 2% sodium pentobarbital (2ml/kg body weight) in the end of experiment.One PE-10 tube filling with heparin was inserted from superior mesenteric vein into portal vein and then connected with pressotransducer to measure pressure.Enterocoelia was exposed totally after mesurement.If ascites was found, dry cotton ball was used to blot liquid and then it was weighted for measurement of ascites.Serum separated from blood which was taken in the vena cava was used for liver function detection.The sample of liver tissue, which was 1.0cm0.8cm0.3cm,was fixed by formalin, embedded by paraffin, and cutted for 4µm thick for HE and collagen staining.Moreover, 100mg liver tissue was used to detect hydroxyproline (Hyp).

Investigating death and ascites in the rats
During making hepatic cirrhosis model, there were no dead rats in week 4 but the death started in week 5. Until the end of week 7, there was still no death in normal group but there were 4 dead rats in control group, 2 dead rats both in FZHY group and in SA-B group, respectively.The reason that leads to death was liver failure.The number of the rats with ascites was most in control group than in other groups.The difference was significantly.

The concentration of Hyp in the liver tissue of cirrhotic rats was decreased by Chinese herb medicine
Compared with normal group, concentration of Hyp in the liver tissue was significantly increased at the end of experiment in controls (P<0.01).The concentration of Hyp, however, was significantly lower both in FZHY group and SA-B group than in controls (P<0.05).(Fig. 7)

Portal vein pressure of the cirrhotic rats was declined and the tissue concentration of ET-1 was dropped by Chinese herb medicine
The portal vein pressure of control rats was significantly increased in the end of experiment compared with normal rats (P<0.01).The increased range was up to 8mmHg.The portal pressure，however, was significantly lower in the rats treated with FZHY Recipe or SA-B than controls (P<0.05).(Fig. 8) The hepatic tissue concentration of ET-1 was obviously higher in controls than in normal group (P<0.01).But concentration of ET-1 was remarkably declined in FZHY group and SA-B group compared with controls (P<0.05).(Fig. 9

Summary
The elevation of portal vein pressure is positively correlated with the increase of ET-1 concentration in the liver tissue during the process of liver cirrhosis.FZHY Recipe and SA-B 3.2 Experiment 2: Chinese herb medicine can relieve capillarization of sinusoid in cirrhotic rats

Aims
To investigate the effects of FZHY Recipe on capillarization of hepatic sinusoids.

Methods
32 Sprague-Dawley male rats, weighing about 150g, were randomly divided into normal group (n=7) and model group (n=25).The modeling mathod was the same as Experiment 1 for making cirrhosis.The cirrhotic rats were more randomly divided into control group (n=11), and FZHY group (n=14).The drug, dose and method of administration for each group were the same as Experiment 1, too.But the duration of treatment was for 4 weeks.
Rat's blood, under etherization condition, was collected from inferior vena cava, and was separated to serum.The sample of liver (1.0cm×0.8cm×0.3cm)was immediately taken and fixed in neutral formalin, embedded in paraffin, sectioned at 5 m thick.The sections of liver were stained with HE, Masson and immunohistochemistry. Three rats were randomly selected from each group respectively for observation of hepatic microstructure.The each liver sample was cut to a 1 mm 3 cube, fixed with 2.5% glutaraldehyde and 1% osmium tetroxide for 2h, embedded with araldite 618, and cut to ultrathin sections.The sections were observed by the electron microscope (H-600).100mg liver tissue was used to detect Hyp.

Fuzheng Huayu Recipe had the potent effect against hepatic fibrosis of the model rat
It was observed that hemorrhage, necrosis and extensive connective tissue hyperplasia in the liver tissues of model rats.The fiber septa reached out its branches towards the liver lobule.(Fig. 10

Fuzheng Huayu Recipe could effectively inhibit sinusoid capillarization in fibrotic rats
It was observed that the structure of sinusoids is clearly and the phenotype of SEC is thin by microscopy in normal group.There were many fenestrae in SEC cytoplasm and no basement membrane covered on SEC in perisinusoid side.In controls, the sinusoids were twisted and narrow, the fenestrae in SEC were reduced or disappeared, and basement membrane was observed.(Fig. 11)Factor Ⅷ related antigen (Ⅷ R•Ag), -smooth muscle actin (-SMA) and laminin (LM), the important indexes for hepatic sinusoid capillarization, were positive staining in liver tissure.But collagen type Ⅳ (Col Ⅳ), which is a composition of functional membrane but not a composition of basement membrane, expressed majorly in fibrous septa and HSC but less and discontinuously in perisinusoids in controls.Compared with controls, however, the narrow sinusoids were reduced and some sinusoids returned to normal phenotype, basement membrane looked discontinuous thiner, and the positive degree of Ⅷ R•Ag, -SMA and LM were lower and their positive area was significantly smaller by image analysis in the liver of FZHY group than in that of controls (P<0.05).Col Ⅳ expressed still continuously in perisinusoids in FZHY group.It indicated that the normal structure of sinusoids was most kept and it meansed that the alteration of hepatic sinusoid capillarization was reversed.(Fig. 12)

Summary
Fuzheng Huayu Recipe had the potent effect on against liver fibrosis.The one of mechanisms of the recipe perhaps is associated with inhibition of hepatic sinusoid capillarization.

Aims
To establish a rat model of portal hypertension induced by ET-1 and investigate the effect of SA-B on decreasing portal vein pressure in the model.

To establish portal hypertension model of rats induced by ET-1
48 Sprague-Dawley male rats were randomly divided into four groups: the NS solution group, the ET-1 low-dose group (0.3g/kg body weight), the ET-1 medium-dose group www.intechopen.com

109
(1.0g/kg body weight) and the ET-1 high-dose group (3.0g/kg body weight).Rats were injected with 200l NS solution into rat via femoral vein by a pump with a rate of 80μl/min in NS solution group.As the same method, rats were injected with 200ml ET-1 solution with the dose of 0.3g/kg body weight, 1.0g/kg body weight or 3.0g/kg body weight respectively in 3 ET-1 groups.Then, monitored the changes of carotid pressure and portal vein pressure in each group at 2min, 4min, 6min, 8min, 10min, 15min, 20min, 25min and 30min after injection.

To treat rats with drugs in portal hypertension models
20 Sprague-Dawley male rats with about 330g body weight were randomly divided into four groups: normal group, SA-B group, BQ-123 (ET A R antagonist) group and BQ-788 (ET B R antagonist) group (n=5 in each group).In normal group, BQ-123 group and BQ-788 group, rats were gavaged with water at a dose of 1ml/100g body weight and rats in SA-B group were gavaged with SA-B solution (containing 125mg/100ml) at the same dose.The gavage was performed twice per day for 5 days.The experiment started at 1 hour after the final gavage.First, via rat's femoral vein, rats was injected with BQ-123 (12.5µg/kg body weight) in BQ-123 group and with BQ-788 (15µg/kg body weight) in BQ-788 group.30min later, rats were injected with a dose (3µg/kg body weight) of ET-1 solution by a pump with rate of 80μl/min in each group.Then, the portal vein pressure was measured before and after injection of ET-1.

To measure carotid pressure, heart rate and portal vein pressure
A piece of PE-50 tube, which full with heparin solution, was inserted into the left carotid artery of the rat.Following that, connect the tube to a pressure transducer in order to measure carotid pressure and heart rate.Then a piece of PE-10 tube, which full with heparin solution, was inserted from superior mesenteric vein to the middle of portal vein.Connect the tube to a pressure transducer for measurement of portal vein pressure.

A kind of model of rat with portal hypertension was successfully established by injection of ET-1
There was no obvious effect of solution volume on carotid pressure and portal vein pressure after injection of NS solution.ET-1 solution with equal volume of NS solution was injected into the rats in low-and medium-dose groups.The carotid pressure was not noticeable rise or fall, only minor fluctuations within 20 min after injection.The carotid pressure, however, was increased slightly after injection of ET-1 in high-dose group but the alteration was not significant (Fig. 13).Portal vein pressure was increased in short time after injection of ET-1 although the alteration was not same in three different dose groups.The alteration of pressure was most remarkable in high-dose group than in others.After reaching to peak level, portal vein pressure was stable for 4min, 4min and 10min in low-, medium-and highdose groups, respectively (Fig. 14 and Tab. 5).The results indicated that the increase of portal vein pressure was solely caused by the injection of ET-1 and without related with the volume of solution in this kind of animal model.This inducing method would not cause a significant increase of systemic blood pressure.Compared with the existing portal vein perfusion model, this kind of portal hypertension model is more similar to the "living" state.
It was also avoided that increase of portal vein pressure caused by sudden increase of partial www.intechopen.com Portal Hypertension -Causes and Complications 110 blood volume by quickly direct injection of ET-1 in portal vein.This kind of model would better reflect the true effect of ET-1 compared with other kind of model.Therefore, this kind of model could use not only for investigation of efficacy and mechanism of drug, but also provided an ideal experimental subject for screening drugs to treat portal hypertension.
NS group low-dose group medium-dose group high-dose group Fig. 13.Effect of ET-1 with different doses on rat carotid pressures After detecting carotic pressure for 5min, NS solution or ET-1 with same volume but different doses were constantly injected and carotic pressure was detected for 30min.The pressure was not increased during detected time in NS group, and low-and medium-dose groups.But the carotid pressure was increased slightly in high-dose group.which were pretreated with SA-B solution by gavage or with BQ-123 or BQ-788 by injection, was also increased after ET-1 injection, however, the ranget-increased was obviously less than that in controls (P<0.01,P<0.001) (Tab.6).Furthermore, the stable time, when portal vein pressure kept high level after reaching peak level, was short in SA-B group.It was just 6 min in SA-B group but was 10min in controls.(Fig. 15) Fig. 15.SA-B could inhibit portal vein pressure of rats induced by ET-1 Portal vein pressure began increase at 5min when starting injection of ET-1.The peak level of pressure was at 9min in SA-B group.Then the pressure kept high level until to at 15min.In controls, however, the pressure continuously increased until to highest peak level at 15min and began to decrease.The pressure level was still hinger (a little bit higher than a peak level in SA-B group) until to at 25min.

Aims
To establish portal hypertension model of mice induced by ET-1 and investigate the effect of SA-B on decreasing portal vein pressure in this kind of model.

To establish a kind of portal hypertension model mice induced by ET-1
36 male Kunming mices, 30±5g body weight, were randomly divided into three groups: control group (n=12), SA-B group (n=12) and blocker group (n=12).Mice were gavaged with SA-B (1mg/ml) in SA-B group and gavaged with water in control group and blocker group.The volume of gvage was 0.5 ml per mouse once a day for 3days.Mice were injected with BQ-123 2g/kg body weight by tail vein at 0.5h before start of below experiment in blocker group.
Mice were injected with ET-1 1.6g/kg body weight at constant velocity by tail vein.6 mice were randomly taken out from each group to measure blood flow volume in liver microcirculation using a laser-Doppler flow instrument before and after injection of ET-1.Other 6 mice in each group were measured the blood flow rate in liver microcirculation by an inverted fluorescence microscope with microscopic live video technology before and after injection of ET-1.

To measure the average blood flow volume in the perfusion of liver microcirculation
Each mouse was injected with 2% pentobarbital sodium solution at a dose of 2ml/kg body weight for anesthesia.After opening abdomen the liver was put on a detector connected with a laser-Doppler flow instrument to record the blood flow volum in the perfusion of liver microcirculation for 5min.After a pause, ET-1 was injected by a syringe pump at a constant rate of 80l/ min through tail vein.Then, the blood flow volum was recorded again for 5min.The average blood flow volume was calculated from the stable datas during the former 5min record and late 5min record, respectively.

To measure the blood flow rate in liver microcirculation
Each mouse was injected with 2% pentobarbital sodium solution at a dose of 2ml/kg body weight for anesthesia.After opening abdomen the liver was put on a piece of glass plate which was on an inverted fluorescence microscope.After 0.05ml pre-labeled erythrocytes with FITC was injected into the inferior vena cava, a suitable site was focused to observe the liver microcirculation.Some FITC-RBCs were observed to be moving quickly in microvasculature or sinusoids and recorded with digital video.ET-1(1.6g/kg body weight) was injected by a syringe pump at a constant rate of 80l/ min through tail vein of mouse then moving FITC-RBCs were immediately recorded again with digital video.The moving range of FITC-RBCs in record was calculated by the analytic software to compare the differences of blood flow rate in liver microcirculation in 3 groups.

Conclusion
The Chinese medicine, Fuzheng Huayu Recipe, is able to reduce portal hypertension in liver cirrhosis both in clinic and in vivo.The effect of Fuzheng Huayu Recipe is related with reversing hepatic fibrosis and capillarization, and decreasing concentration of ET-1 in the liver tissue.SA-B is an extracted component of Fuzheng Huayu Recipe.Several studies showed that the effect in SA-B was similar to Fuzheng Huayu Recipe on reversing hepatic fibrosis and decreasing concentration of ET-1 in the liver tissue.SA-B inhibited contraction of HSC through suppressing the intracellular concentration of [Ca 2+ ]i.Based on above effects, intrahepatic vessel resistance was reduced which leaded to improve liver microcirculation.It has distinctively character that Chinese herb medicine is used to treat hepatic portal hypertension which is caused by failure of liver microcirculation in chronic liver diseases.

Fig.
Fig.3.Actuarial probability of remaining free of esophageal variceal bleeding in cirrhotic patients with moderate and severe varices level The patients were treated with Fuzheng Huayu Capsule in FZHYC group, Propranolol in Propranolol group, or hoth in combination group for 24 months.Actuarial probability of remaining free of esophageal variceal bleeding was higher in combination group and FZHYC group than in Propranolol group.Compared with Propranolol group, the difference was significant in combination group (P<0.01) and in FZHYC group (P<0.05).Although the probability was higher in combination group than in FZHYC group, but the difference was not significant.

Fig. 4 .
Fig. 4. Fuzheng Huayu Recipe and SA-B could relieve inflammation and structure damage in the liver tissue of DMN model rats A: normal group, B: control group, C: FZHY group and D: SA-B group.The staining was by HE (200).
the cirrhosis-induced elevation of portal vein pressure and concentration of ET-1 in the liver tissue through their effect on anti-fibrosis in the liver.

Fig. 11 .
Fig. 11.Fuzheng Huayu Recipe could inhibit sinusoid capillarization by observation of electron micrographs S: sinusoid; C: collagen.A: Hepatic sinusoid appeare as a typical capillary surrounded by continuous basement membrane.(arrow's heads indicated) in the liver of fibrotic rat.The perisinusoid is stenosis (arrows indicated) and microvilli of hepatocyte are almost absent in the space (15000×).B: Sinusoid capillarization is not formed in the liver of rat treated with Fuzheng Huayu Recipe.The fenestrae are observed (arrow's heads indicated) in cytoplasm of SEC.A mass of microvilli of hepatocyte stretchs into perisinusoid is exist (arrow indicated) but basement membrane is absent (10000×).

Fig. 12 .
Fig. 12. Fuzheng Huayu Recipe could alter the express of indexes for hepatic sinusoid capillarization by immunohistochemistry staining in fibrotic liver of rats Arrows show the positive area.A: Ⅷ R•Ag is around the vessels with strong staining in controls.B: The positive area of Ⅷ R•Ag is decreased in FZHY group.C: Col Ⅳ expresses majorly in fibrous septa and HSC but less and discontinuously in perisinusoids in controls.D: Col Ⅳ expresses almost continuously in perisinusoids in FZHY group.E: The express of LM is observed on the wall of vessels and sinusoids in the liver of controls.F: The express of LM is only observed on the wall of vessels in the liver of FZHY group.G: -SMA expresses strongly in perisinusoids, HSC and fibous septa in controls.H: -SMA expresses dramaticlly less in FZHY group (100×).

Fig. 17
Fig.17.The morphological changes of HSC in each group a: serum-free group; b: ET group; c: low-dose group; d: medium-dose group; e: high-dose group.HSC grew exuberantly on gel and the pseudopodium of HSC was a lot, thin and long in serum-free group.After induced by ET-1 for 12h, however, HSC became obviously small with contraction.The quantity and the pseudopodium of HSC was decreased in ET group.The phenotype of HSC in low-dose group was similar to that in ET group.The phenotype of HSC in high-dose group was similar to that in serum-free group.The phenotype of HSC in medium-dose group was between the low-and high-dose groups (By OLYMPUS I × 50 / I × 70 inverted system microscope, Japan, 200×).
Fig.17.The morphological changes of HSC in each group a: serum-free group; b: ET group; c: low-dose group; d: medium-dose group; e: high-dose group.HSC grew exuberantly on gel and the pseudopodium of HSC was a lot, thin and long in serum-free group.After induced by ET-1 for 12h, however, HSC became obviously small with contraction.The quantity and the pseudopodium of HSC was decreased in ET group.The phenotype of HSC in low-dose group was similar to that in ET group.The phenotype of HSC in high-dose group was similar to that in serum-free group.The phenotype of HSC in medium-dose group was between the low-and high-dose groups (By OLYMPUS I × 50 / I × 70 inverted system microscope, Japan, 200×).

Table 2 .
The situation of death and ascites in cirrhotic rats in each group

2 Observation of Pathology of liver in rats 3.1.3.2.1 Inflammation was reduced by Chinese herb medicine in the liver of cirrhotic rats
The structure of liver lobule was clear, hepatocytes arranged as cords radially from central vein to the periphery and a few connective tissue was observed in the portal area in normal group.At the end of treatment, pathological alteration was observed in the liver that was

Hepatic fibrosis was reversed by Chinese herb medicine A
little collagen fibers located only in portal areas or surrounded central veins in normal rat liver.Increased fibrous tissue formed thick interval that invaded into the hepatic lobules and moved round to form pseudolobules with different size in controls'liver.The fibrous intervals were thinner both in FZHY group and SA-B group than in controls.It means that hepatic fibrosis was reversed by FZHY recipe and SA-B.(Fig.5)

3 The liver function of cirrhotic rats can be improved by Chinese herb medicine
Compared with normal rats, it was significantly increased in controls that are the activity of serum ALT and AST, serum level of TBiL P<0.01 and P<0.05 but meanwhile the concentration of serum Alb were significantly decreased P<0.05 .However, they were obviously lower both in FZHY group and SA-B group than in controls that are the activity of serum ALT and AST P<0.01 , and serum level of TBiL P<0.05 .The concentration of serum Alb were back to normal level with significantly difference compared with controls (P <0.05).(Fig.6) .)

Table 3 .
Hyperplasia degree of collagenous fibers in each group and Tab. 3) The level of hydroxyproline was significantly increased.Compared with controls, liver inflammation, necrosis of hepatocytes and hepatic fibrosis was reduced in FZHY group.The concentration of liver hydroxyproline was significantly lower in FZHY group than in controls (P<0.05).(Tab.4)www.intechopen.comTraditionalChinese Medicine Can Improve Liver Microcirculation and Reduce Portal Hypertension in Liver Cirrhosis 105 Fig. 10.Fuzheng Huayu Recipe inhibited hepatic fibrosis The liver sections were stained with Masson and showed hepatic fibrosis.A: Fibrous septa (arrows indicated) and pseudolobule (arrow's head indicated) have formed in controls.B: Fibrous septa (arrow indicated) is less and pseudolobule is absent in FZHY group (100×).Note: compared with normal, *: P<0.05; compared with controls, #: P<0.05Table 4. Liver Hydroxyproline level in liver tissues ( x ±s) Effect of ET-1 with different doses on rat portal vein pressure After detecting portal vein pressure for 5min, NS solution and ET-1 with same volume but different doses were constantly injected and portal vein pressure was detected for 30min.There was no obvious effect of NS solution on portal vein pressure.The pressure was increased at 5min when starting injection of ET-1 and kept high level for 4min, 4min and 10min in low-, mediumand high-dose groups after the pressure reaching to a peak level at 9 min, respectively.

Table 5 .
Effect of ET-1 with different doses on portal vein pressure of rats (X±S)

Table 7 .
Compare of the carotid artery pressure and heart rate in SA-B group and controls

did not affect on carotid pressure and heart rate in normal rat
Rats were pretreated with SA-B solution by gavage for 5d, but the carotid pressure and heart rate were no significant different between in SA-B group and controls.(Tab.7)