Study on effect of scutellarin in resisting liver fibrosis in rats.
- Author:
Yin-hui WANG
;
Ling GENG
;
Hui LI
- Publication Type:Journal Article
- MeSH:
Alanine Transaminase;
genetics;
metabolism;
Animals;
Apigenin;
administration & dosage;
Bilirubin;
genetics;
metabolism;
Collagen Type IV;
genetics;
metabolism;
Drugs, Chinese Herbal;
administration & dosage;
Glucuronates;
administration & dosage;
Humans;
Liver;
drug effects;
enzymology;
metabolism;
Liver Cirrhosis;
drug therapy;
genetics;
metabolism;
Male;
Rats;
Rats, Sprague-Dawley
- From:
China Journal of Chinese Materia Medica
2015;40(10):1999-2003
- CountryChina
- Language:Chinese
-
Abstract:
Totally 80 rats were randomly divided into the control group, the model group, low, middle and high dose (25, 50, 100 mg x kg(-1)) scutellarin( SC) groups and the colchicine ( Col) group. Apart from the blank group, all of the remaining groups were intraperitoneally injected with 0.5 mL pig serum twice every week for consecutively 13 weeks and orally administered with the corresponding drugs since the 9th week. The blank group and the model group were orally given equal volume of normal saline once every for consecutively four weeks. After the experiment, efforts were made to detect the contents of alanine aminotransferase (ALT), aspertate aminotransferase (AST), albumin (ALB), total protein (TP), total bilirubin (TBIL), hyaluronic acid (HA), laminin (LN) and collagen type IV (CIV), collect liver tissues of fixed positions, observe the pathological changes through hematoxylin-eosin (HE) staining, conduct the pathological grading for liver fibrosis, determine the expressions of hepatic collagen type I and III (C I, C III) and calculate their color rendering index. Compared with the model group, low, middle and high dose (25, 50, 100 mg x kg(-1)) SC groups could decrease the contents of ALT, AST, TBIL, HA, LN, CIV, increase the contents of ALB, TP in serum and reduce the contents of C I, C III in liver tissues. In conclusion, scutellarin has a certain therapeutic effect on immune liver fibrosis in rats induced by pig serum.