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Effect of Astragalus complanatus flavonoid on anti-liver fibrosis in rats

Effect of Astragalus complanatus flavonoid on anti-liver fibrosis in rats

作     者:Chun-Yu Liu Zhen-Lun Gu Wen-Xuan Zhou Ci-Yi Guo 

作者机构:Department of Pharmacology Medical College of Suzhou University Suzhou 215007 Jiangsu Province China Suzhou Institute of Chinese Meteria Medica Suzhou University Suzhou 215007 Jiangsu Province China The Hong Kong Association for Health Care Ltd Hong Kong China 

出 版 物:《World Journal of Gastroenterology》 (世界胃肠病学杂志(英文版))

年 卷 期:2005年第11卷第37期

页      面:5782-5786页

核心收录:

学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学] 

主  题:Astragalus complanatus, Liver fibrosis N-propeptide of typeⅠ procollagen N-propeptide of type Ⅲ procollagen Malondialdehyde Superoxide dismutase Matrix metal protease-1 Tissue inhibitor of metal protease-1 

摘      要:AIM: To observe the anti-liver fibrosis effect of Astragalus complanatus fiavonoids (ACF) in rats. METHODS: The liver fibrosis model in rats was established by injecting interperitoneally 0.2 mL/100 g 0.5% dimethylnitrosamine, thrice a week. Meanwhile, the rats were administered ACF (30, 60, 120 mg/kg) or colchicine (0.1 mg/kg) once a day for 1 mo. Serum N-propeptide of type Ⅰ procollagen (PINP) and type Ⅲ procollagen (PⅢNP) was measured using ELISA. Malondialdehyde (MDA) and superoxide dismutase (SOD) in hepatic tissue were evaluated. Matrix metal protease-1 (MMP-1) mRNA expression was assayed by RT-PCR and the protein expression of tissue inhibitor of metal protease-1 (TIMP-1) was analyzed by immunohistochemistry. RESULTS: In the ACF groups, SOD activity increased and MDA content decreased in comparison to the liver fibrosis model group. The serum PINP and PⅢNP contents in ACF-2 and -3 group decreased compared to those in model group. In ACF-2 and -3 group, the expression of MMP-1 mRNA increased significantly and the protein expression of TIMP-1 decreased compared to that in model group. CONCLUSION: The antifibrotic mechanisms of ACF are associated with its influence on lipid peroxidation and collagen synthesis and degradation.

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