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机构地区:[1]新疆医科大学药学院药剂学教研室,新疆乌鲁木齐830054
出 处:《新疆医科大学学报》2006年第5期421-423,共3页Journal of Xinjiang Medical University
摘 要:目的:研究水飞蓟素脂质体(L-SIL)对四氯化碳(CCl4)所致小鼠急性肝损伤的保护作用.方法:昆明种小鼠80只,随机分为空白组、CCl4急性肝损伤模型组及L-SIL低、中、高剂量组和益肝灵(T-SIL)低、中、高剂量组共8组,测量并比较各组小鼠血清丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)水平及肝组织匀浆中超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)水平和丙二醛(MDA)含量,并观察各组小鼠肝组织病理学改变.结果:与CCl4急性肝损伤模型组相比,L-SIL各剂量组血清ALT、AST水平明显降低(P〈0.05~0.01),L-SIL各剂量肝组织匀浆GSH-PX水平及L-SIL高剂量组SOD水平明显升高(P〈0.05~0.01),并具有剂量依赖性,L-SIL高剂量组肝组织匀浆MDA含量明显降低(P〈0.01).L-SIL对ALT、SOD、GSH-PX水平的作用优于相应剂量T-SIL组(P〈0.05~0.01).组织学观察L-SIL中、大剂量组的肝损伤明显轻于模型组和相应剂量T-SIL组.结论:L-SIL对小鼠CCl4肝损伤有明显的保护作用,且其保护作用明显优于T-SIL.Objective: To investigate the protective effect of silymarin liposomes(L-SIL) on the CCl4 in duced acute liver injury in mice. Methods: Kun ruing mice were randomly divided into normal control group, model control group, high, middle and low dose groups of L-SIL and high, middle and low dose groups of T-SIL. The model of hepatic damage were induced by CCl4. The Alanine aminotransferase (ALT), Aspartate aminotransferase(AST) levels in serum , malondialdehyde(MDA) content, superoxide dismutase(SOD), glutathione peroxidase(GSH-PX) levels in liver homogenate were examined and dimensions of hepatic damage in the histopathology were observed. Results: L-SIL could inhibit the rising of set um ALT, AST levels caused by CCl4 in dose-response manner (P 〈0.05-0.01). Meanwhile, L-SIL also decreased MDA content (P 〈0. 01) and prevented the reduction of SOD, GSH-PX levels in the liver ho mogenate (P 〈0. 05-0.01). The effects of L-SIL on the ALT level in serum and SOD, GSH-PX levels in liver homogenate against experimental liver injury in mice were more powerful than that of T-SIL of the same dose (P 〈0. 05-0.01). The liver pathological observation showed that the liver injury of L-SIL (150,300 mg/kg. d) were significantly less than that of the model group and T- SIL of the same dose. Conclusion: The protective effect of L-SIL on the CCl4 induced acute liver injury in mice was more potent than that of T-SIL in the same dose.
分 类 号:Q949.783.5[生物学—植物学] R-332[医药卫生]
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