Anti-fibrotic effects of Acremoniumterricola milleretal mycelium on immunological hepatic fibrosis in rats

被引:6
作者
Li, Xia [1 ,2 ]
He, Can [1 ]
Wu, Wang-Yang [1 ]
Huang, Huan [1 ]
Li, Wei-Zu [1 ]
Yin, Yan-Yan [1 ]
机构
[1] Anhui Med Univ, Dept Pharmacol, Hefei 230032, Anhui, Peoples R China
[2] Anhui Prov Feidong Country Peoples Hosp, Dept Pharm, Feidong 231600, Anhui, Peoples R China
关键词
Acremoniumterricola milleretal mycelium; porcine serum; liver fibrosis; transforming growth factor-beta/Smad; LIVER FIBROSIS; STELLATE CELLS; FIBROGENESIS; EXPRESSION; CIRRHOSIS; DISEASE; ALPHA; BETA; SMAD; PATHOGENESIS;
D O I
10.3892/mmr.2014.2604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acremoniumterricola milleretal mycelium (A MM) exerts numerous protective effects on organs, and has been used in Chinese herb prescriptions to treat refractory diseases. The aim of this study was to investigate the effects of AMM on immunological hepatic fibrosis induced by porcine serum (PS) in rats. Male Sprague Dawley rats were administered 0.5 ml sterile PS by intraperitoneal injections twice a week for 18 weeks. AMM (175, 350 or 700 mg/kg) and colchicine (0.1 mg/kg) were administered intragastrically each day until the rats were sacrificed. PS administration resulted in marked hepatic fibrosis, as assessed by increased oxidative stress and hepatic collagen content, as well as a-smooth muscle actin (alpha-SMA) expression. A MM significantly reduced liver damage and fibrosis. In addition, AMM decreased the elevation in hydroxyproline, hyaluronic acid, laminin and procollagen type III; increased the activity of superoxide dismutase and glutathione peroxidase; decreased alpha-SMA expression; and eliminated hepatic collagen deposits. Furthermore, AMM inhibited Smad2/3 phosphorylation and Smad7 expression. These results indicate that AMM is able to reduce oxidative stress, inhibit collagen synthesis and block the transforming growth factor-beta/Smad signaling pathway in a dose-dependent manner.
引用
收藏
页码:3327 / 3333
页数:7
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