CHENG Xin-yan. Protective Effect of Total Flavonoids of Bidens on Acute Liver Injury Induced by -GalN in Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(14): 268-271.
CHENG Xin-yan. Protective Effect of Total Flavonoids of Bidens on Acute Liver Injury Induced by -GalN in Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(14): 268-271. DOI: 10.11653/syfj2013140268.
Western blot法检测肝脏中诱导型一氧化氮合酶(iNOS)的表达。HE染色观察肝组织病理学改变。 结果: 与模型组比较
TFB能明显提高D-GalN致急性肝损伤小鼠胸腺、脾脏、肝脏指数(P<0.01)
同时降低血清中ALT
AST
AKP活性(P<0.01)
并增加Alb
T-AOC含量(P<0.01)
降低iNOS的表达(P<0.01)
并减轻肝损伤程度。 结论: 鬼针草总黄酮对D-GalN所致急性肝损伤小鼠有一定保护作用
其机制可能与抗氧化作用和抑制细胞毒作用有关。
Abstract
Objective: To study the protective effect of the total flavonoids of bidens (TFB) on the D-GalN induced acute liver injury in mice. Method: Acute liver injury in mice was established by intraperitoneal injection of D-GalN. The mice were randomly divided into five groups:model group
bifendate group (120 mg·kg-1)
low
medium
high-dosage groups of TFB (60
120
240 mg·kg-1). A normal control group was set up also. The index of thymus
spleen and liver were measured. The serum levels of alanine aminotransferase (ALT)
aspartate aminotransferase (AST) and alkaline phosphatase (AKP)
serum contents of albumin (Alb) and total antioxidant capacity (T-AOC) were examined using colorimetric detection. And the expression of inducibility nitric oxide synthase (iNOS) in liver tissue was determined by western blot analysis. Pathomorphological changes in microscopic slodes were observed by hematoxylin-eosin staining (HE). Result: Compared to model group
TFB markedly increased the index of thymus
spleen
and liver (P<0.01)
and lowered the serum levels of ALT
AST and AKP (P<0.01)
while elevated the contents of Alb
T-AOC (P<0.01)
down-regulated the expression of iNOS (P<0.01)
and alleviated the liver damage condition. Conclusion: The total flavonoids of bidens has protective effect on the D-GalN induced liver injury in mice. The mechanism may be related to antioxidation and inhibition of cytotoxicity.