Protective effect of Acai berries on chronic alcoholic hepatic injury in rats and their effect on inflammatory cytokines.
- Author:
Sheng-sheng QU
;
Jian-jun ZHANG
;
Yan-xia LI
;
Yuan ZHENG
;
Ying-li ZHU
;
Lin-yuan WANG
- Publication Type:Journal Article
- MeSH: Alanine Transaminase; blood; Animals; Aspartate Aminotransferases; blood; Chronic Disease; Cytokines; blood; Euterpe; chemistry; Hepatocytes; drug effects; Interleukin-6; blood; Lipid Peroxidation; drug effects; Liver; drug effects; Liver Diseases, Alcoholic; metabolism; pathology; prevention & control; Male; Plant Extracts; pharmacology; Rats; Rats, Wistar; Triglycerides; blood; Tumor Necrosis Factor-alpha; blood
- From: China Journal of Chinese Materia Medica 2014;39(24):4869-4872
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the protective effect of Acai berries(Euterpe oleraceae) on chronic alcoholic hepatic injury in rats and their mechanism.
METHODWistar rats were fed for 1 week and randomly divided into blank group, model group, Dongbao Gantai group, Acai 1.6, 0.8, 0.4 g . kg-1 groups. The blank group was given distilled water, and the other groups were orally given 56% white spirit (Erguotou) for eight weeks at the dosages of 8 mL . kg-1 in the 1st week, which increased by 0.1 mL week by week till to 15 mL . kg-1, in order to establish the chronic hepatic injury model, and observe the effect of Acai berry freeze-dried powder on hepatocyte membrane permeability, liver lipid peroxidation, changes in inflammatory cytokines and pathological changes in hepatocytes.
RESULTAcai berries could significantly reduce serum ALT and AST(P<0.05), MDA(P<0.05), TG(P<0.05) and serum TNF-α and IL-6(P <0.05) and increase GSH and SOD(P <0.05). According to liver histopathological observation, livers in the model group were dominated by steatosis, some livers suffered spotty necrosis and inflammatory cell infiltration; The positive drug and Acai groups showed different changes in pathologic changes in rat livers.
CONCLUSIONAcai berries show s specific protective effect on alcoholic hepatic injury. Its mechanism may be correlated with the inhibition of such inflammatory factors as TNF-α and IL-6.