| Literature DB >> 29684859 |
Xiya Lu1, Tong Liu2, Kan Chen3, Yujing Xia4, Weiqi Dai5, Shizan Xu6, Ling Xu7, Fan Wang8, Liwei Wu9, Jingjing Li10, Sainan Li11, Wenwen Wang12, Qiang Yu13, Jiao Feng14, Xiaoming Fan15, Yingqun Zhou16, Peiqin Niu17, Chuanyong Guo18.
Abstract
Isorhamnetin, a flavonoid compound extracted from plants' fruit or leaves, like sea buckthorn (Hippophae rhamnoides L.), has many biological functions, including anti-tumor, anti-oxidant and anti-inflammatory effect. The present study is in order to explore the hepatoprotective effect of isorhamnetin on concanavalin A (ConA)-induced acute fulminant hepatitis and the underlying mechanism. Mice were injected with ConA (25 mg/kg) to induce acute fulminant hepatitis, three doses of isorhamnetin (10/30/90 mg/kg) was intraperitoneally administrated about 1 h previously. The serum and liver tissues were harvested at 2, 8, and 24 h after ConA injection. The levels of serum liver enzymes and proinflammatory cytokines were significantly reduced in isorhamnetin administration groups. Besides, isorhamnetin improved pathological damage. Furthermore, isorhamnetin affected P38/PPAR-α pathway, and subsequently regulated the expression of apoptosis and autophagy related proteins. The present study investigated that isorhamnetin inhibits apoptosis and autophagy via P38/PPAR-α pathway in mice.Entities:
Keywords: 3-methylquercetin; Apoptosis; Autophagy; Concanavalin A; Hepatitis
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Year: 2018 PMID: 29684859 DOI: 10.1016/j.biopha.2018.04.016
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529