期刊文献+

东宝肝泰片防治大鼠酒精性脂肪肝的作用及机制研究 被引量:7

Action Mechanism of Dongbaogantai Tablet in the Prevention and Treatment of Alcoholic Fatty Liver in Rats
原文传递
导出
摘要 目的:研究东宝肝泰片对酒精性脂肪肝(AFL)模型大鼠的防治作用及机制。方法:取SD大鼠随机分成正常组、模型组和东宝肝泰片组,后2组用白酒灌胃和高脂饲料喂养共8周以复制大鼠AFL模型,同时分别给予生理盐水和东宝肝泰片灌胃8周,测定各组大鼠血清甘油三酯(TG)、胆固醇(CHO)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)水平,天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)活性,肝组织中丙二醛(MDA)、游离脂肪酸(NEFA)含量和超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)活性,光镜下观察大鼠肝脏的病理变化。结果:与模型组比较,东宝肝泰片组TG、CHO、LDL-C、AST、ALT、MDA、NEFA水平显著降低(P<0.05),HDL-C、SOD、GSH-PX水平显著升高(P<0.05),其肝脏病理与正常组相似。结论:东宝肝泰片可通过减轻脂质过氧化反应有效防治AFL。 OBJECTIVE: To investigate the mechanism of the prevention and treatment effects of dongbaogantai tablet (DT) on rats with alcoholic fatty liver (AFL) . METHODS: SD rats were randomly divided into normal control group, model group and DT group. The model group and DT group were administered intragastrically with alcohol and fed with high fat diet for 8 weeks to replicate AFL model, meanwhile the model group were administered intragastrically with normal saline and DT group with DT synchronously for 8 weeks. Levels of TG, CHO, LDL- C, HDL - C, AST and ALT in serum, and MDA, NEFA, SOD and GSH- PX in hepatic tissue were detected and the pathological changes of liver were observed under light microscope. RESULTS: In DT group compared with model group, serum levels of TG, CHO, LDL - C, AST, ALT, MDA and NEFA were significantly down - regulated (P 〈0.05), but levels of HDL - C, SOD and GSH - PX were significantly up - regulated (P〈0.05); however, the pathological changes of liver were similar to those in normal control group. CONCLUSION: DT can effectively prevent and treat AFL by reducing the lipid peroxidation.
出处 《中国药房》 CAS CSCD 北大核心 2009年第28期2179-2181,共3页 China Pharmacy
基金 江西省卫生厅中医药科研计划项目(2003A59)
关键词 东宝肝泰片 酒精性脂肪肝 防治 大鼠 Dongbaogantai tablet Alcoholic fatty liver Prevention and treatment Rat
  • 相关文献

参考文献6

二级参考文献18

  • 1张宇,陈韶华,张幸国,任国平,萨小婴,虞朝辉,厉有名.茶多酚治疗慢性酒精性肝损伤的实验研究[J].中华肝脏病杂志,2005,13(2):125-127. 被引量:15
  • 2Lieber C S,DeCarli L M.The feeding of ethanol inliquid diets:1986[J].Alcohol Clin Exp Res,1986; 10(5):550-553.
  • 3Yokoyama H,Nagata S,Moriya S,et al.Hepatic fibrosis produced in guinea pigs by chronic tehanol administration and immunization with acetadehyde adducts[J].Hepatology,1995;21(5):1438-1442.
  • 4Tsukamoto H,Reidelberger R D,French S W,et al.Long-term cannulation model for blood sampling and intragastric infusion in the rat[J].Am J Physiol,1984; 247(3Pt2):R595-R599.
  • 5Tsukamoto H,Horne W,Kamimura S,et al.Experimental liver cirrhosis induced by alcohol and iron[J].J Clin Invest,1995;96(1):620-630.
  • 6Lindros KO,Stowell L,Vaanaoen H,et al.Uninterrupted prolonged ethanol oxidation as a main pathogenetic factor of alcoholic liver damage evidence from new liquid diet animal[J].Liver,1983; 3(2):79-91.
  • 7Rubin E,Lieber CS.Fatty liver,alcoholic hepatitis and cirrhosis produced by alcohol in primates[J].N Eng J Med,1974;290(3):128-135.
  • 8倪燕君.脂肪肝的发病机理和诊断治疗研究进展[J].国外医学(消化系疾病分册),1997,17(3):158-162. 被引量:138
  • 9范建高,曾民德,钟岚,徐正婕,王国良.牛磺酸、金牡蛎对大鼠酒精性肝损伤的防治作用[J].肝脏,1999,4(3):154-156. 被引量:23
  • 10李东良,王玉玫.大鼠酒精性肝损伤模型的建立及病理学观察[J].实用肝脏病杂志,1998,3(4):207-208. 被引量:15

共引文献47

同被引文献28

引证文献7

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部