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机构地区:[1]中国药科大学药学院药理学教研室 [2]中国药科大学新药研究中心
出 处:《中国临床药理学与治疗学》2005年第11期1261-1265,共5页Chinese Journal of Clinical Pharmacology and Therapeutics
摘 要:目的:观察一氧化氮供体型齐墩果酸衍生物ZCⅡ2对早期实验性肝纤维化的保护作用。方法:用CCl4诱导大鼠肝纤维化模型,ZCⅡ2以128mg·kg-1和64mg·kg-1的剂量给大鼠连续灌胃给药30d,测定血清总蛋白(TP)、白蛋白(ALB)、谷丙转氨酶(ALT)、谷草转氨酶(AST)、一氧化氮(NO)以及血清透明质酸(HA)、层粘蛋白(LN)和Ⅲ型前胶原(PCⅢ)的含量,计算白蛋白与球蛋白的比例(白球比例);测定肝组织中丙二醛(MDA)和谷胱甘肽过氧化物酶(GSHPx)及一氧化氮合酶(NOS)的含量,并行肝组织病理组织学检查。结果:与模型组相比,ZCⅡ2高剂量能显著降低谷丙转氨酶、谷草转氨酶含量,增加白蛋白含量,提高白球比例,显著降低血清透明质酸、层粘蛋白和Ⅲ型前胶原含量,明显改善肝组织病理损伤。结论:一氧化氮供体型齐墩果酸衍生物ZCⅡ2对大鼠早期实验性肝纤维化具有一定的保护作用。AIM: To investigate protect effect of the NO donating-oleanlic acid derivatives on hepatic fibrosis in rats. METHODS: The rat model with early hepatic fibrosis was induced by carbon tetrachloride (CC14). ZC Ⅱ 2 at the dose of 128 and 64 mg·kg^-1 had been given orally for 30 days. Serum level of the total protein (TP), albumin (ALB), the albumin/globulin (A/G) and ALT, AST. The hyaluronic acid (HA), laminin (LN), the procollagen type Ⅲ (PCⅢ) and the level of MDA, GSHPx in liver tissues were detemained. Pathological examination to reveal the extent of liver damages was observed. RESULTS : ZC Ⅱ 2 at the dose of 128 mg·kg^- 1 increased the serum TP, ALB, and A/G and decreased HA, LN, PC IH, ALT, and AST more significantly than the model group, and hepatic pathological injury was abated to some degree. CONCLUSIONS: ZCⅡ2 at the dose of 128mg·kg^-1 can attenuate liver damages, protect against lipoperoxidation and attenuate hepatic fibrosis induced by CCl4.
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