ZHANG Ying-li, FAN Ying, ZI Hui, et al. Protective Effects of Baogan Granules on Acute Alcohol-induced Liver Injury in Mice[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(12): 108-111.
DOI:
ZHANG Ying-li, FAN Ying, ZI Hui, et al. Protective Effects of Baogan Granules on Acute Alcohol-induced Liver Injury in Mice[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(12): 108-111. DOI: 10.13422/j.cnki.syfjx.2015120108.
Protective Effects of Baogan Granules on Acute Alcohol-induced Liver Injury in Mice
Objective: To observe the protective effect of Baogan granules on acute alcoholic-induced liver injury in mice. Method: The experimental mice were randomly divided into the normal group
the model group
the Hugan tablet group (0.7 g·kg·d-1)
the Like group (1.18 g·kg-1·d-1)
the high-
medium-
and low-dose Baogan granules groups (12.9
6.45
3.225 g·kg-1·d-1). The mice in the normal and model groups received an equal volume of saline. All mice received 30-day oral administration of the corresponding medicines. The acute liver injury model was induced in mice by feeding 50% alcohol at 0.012 mL·g-1 1 h later after the last administration. The serum levels of alanine aminotransferase (ALT)
aspartic transaminase (AST)
total bilirubin (TBIL)
triglyceride (TG)
high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were detected. Histopathological changes of liver tissue were observed by using the HE staining. Result: Compared with the model control group
the levels of ALT
AST
TBIL
TG and LDL increased
the level of HDL decreased in the model group (P<0.05
P<0.01). Compared with model group
the levels of ALT
AST
TBIL
TG and LDL decreased
the level of HDL increased in the high-
medium-
and low-dose Baogan granules groups (P<0.05
P<0.01). Pathological results showed that the liver cell morphology
structure
edema and inflammatory infiltration had different degrees of improvement in the Baogan granules groups. Conclusion: Baogan granules could obviously inhibit the serum levels of ALT
AST
TG and LDL; promote the HDL generation in mice. However
its effect on TBI is unclear. Moreover
it could protect the alcoholic-induced liver injury by improving liver edema and inflammatory cell infiltration.