前往化源商城

Oxidative Medicine & Cellular Longevity 2015-01-01

Rimonabant Improves Oxidative/Nitrosative Stress in Mice with Nonalcoholic Fatty Liver Disease.

Bojan Jorgačević, Dušan Mladenović, Milica Ninković, Milena Vesković, Vesna Dragutinović, Aleksandar Vatazević, Danijela Vučević, Rada Ješić Vukićević, Tatjana Radosavljević

文献索引:Oxid. Med. Cell. Longev. 2015 , 842108, (2015)

全文:HTML全文

摘要

The present study deals with the effects of rimonabant on oxidative/nitrosative stress in high diet- (HFD-) induced experimental nonalcoholic fatty liver disease (NAFLD). Male mice C57BL/6 were divided into the following groups: control group fed with control diet for 20 weeks (C; n = 6); group fed with HFD for 20 weeks (HF; n = 6); group fed with standard diet and treated with rimonabant after 18 weeks (R; n = 9); group fed with HFD and treated with rimonabant after 18 weeks (HFR; n = 10). Daily dose of rimonabant (10 mg/kg) was administered to HFR and R group by oral gavage for two weeks. Treatment induced a decrease in hepatic malondialdehyde concentration in HFR group compared to HF group (P < 0.01). The concentration of nitrites + nitrates in liver was decreased in HFR group compared to HF group (P < 0.01). Liver content of reduced glutathione was higher in HFR group compared to HF group (P < 0.01). Total liver superoxide dismutase activity in HFR group was decreased in comparison with HF group (P < 0.01). It was found that rimonabant may influence hepatic iron, zinc, copper, and manganese status. Our study indicates potential usefulness of cannabinoid receptor type 1 blockade in the treatment of HFD-induced NAFLD.

相关化合物

结构式 名称/CAS号 全部文献
纯碱 结构式 纯碱
CAS:497-19-8
锰 结构式
CAS:7439-96-5
乙二胺四乙酸 结构式 乙二胺四乙酸
CAS:60-00-4