Title of article :
The antiapoptotic effects of different doses of β-carotene in chronic ethanol-fed rats
Author/Authors :
peng, hsiang-chi taipei medical university - school of nutrition and health sciences, Taipei, Taiwan , chen, ya-ling taipei medical university - school of nutrition and health sciences, Taipei, Taiwan , yang, shin-yi i-shou university - department of nutrition, Kaohsiung, Taiwan , ho, pei-yin national taiwan university - graduate institute of oncology, Taipei, Taiwan , yang, sien-sing cathay general hospital - liver center, Taipei, Taiwan , hu, jui-ting cathay general hospital - liver unit, Taipei, Taiwan , yang, suh- ching taipei medical university - school of nutrition and health sciences, Taipei, Taiwan
From page :
132
To page :
141
Abstract :
Background: Ethanol consumption might induce hepatic apoptosis and cause liver damage. The study wasto investigate the effects of different doses of β-carotene supplementation on the antioxidant capacity andhepatic apoptosis in chronic ethanol-fed rats.Methods: Rats were divided into 6 groups: C (control liquid diet), CLB [control liquid diet with β-carotenesupplementation at 0.52 mg/kg body weight (BW)/day], CHB (control liquid diet with β-carotenesupplementation at 2.6 mg/kg BW/day), E (ethanol liquid diet), ELB (ethanol liquid diet with β-carotenesupplementation at 0.52 mg/kg BW/day), and EHB (ethanol liquid diet with β-carotene supplementationat 2.6 mg/kg BW/day). After 12 weeks, rats were sacrificed and blood and liver samples were collected foranalysis.Results: Lipid peroxidation and hepatic cytochrome P450 2E1 (CYP2E1) expression had increased, andhepatic Fas ligand, caspase-8, cytochrome c, caspase-9, and -3 expressions had significantly increased in theE group. However, lipid peroxidation and CYP2E1, caspase-9, and -3 expressions were significantly lowerand Bcl-xL expression was higher in the ELB group. The hepatic tumor necrosis factor (TNF)-α level, lipidperoxidation, and cytochrome c expression were significantly lower and Bcl-2 expression was significantlyhigher in the EHB group.Conclusions: The results suggest that ethanol treatment causes oxidative stress and hepatic apoptosisleading to liver injury, and β-carotene supplementation (0.52 mg/kg BW/day) can prevent ethanol-inducedliver damage by decreasing ethanol-induced oxidative stress and inhibiting apoptosis in the liver.
Keywords :
Alcoholic liver disease (ALD) , antioxidative stress , apoptosis , β , carotene , rat
Journal title :
Hepatobiliary Surgery an‎d Nutrition
Journal title :
Hepatobiliary Surgery an‎d Nutrition
Record number :
2653822
Link To Document :
بازگشت