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低分子肝素对高脂饮食大鼠非酒精性脂肪性肝炎模型的影响
引用本文:孙林林,石军,郝菁华,任万华. 低分子肝素对高脂饮食大鼠非酒精性脂肪性肝炎模型的影响[J]. 山东大学学报(医学版), 2010, 48(11): 58-62
作者姓名:孙林林  石军  郝菁华  任万华
作者单位:山东大学附属省立医院肝病中心,济南,250021;山东大学附属省立医院肝病中心,济南,250021;山东大学附属省立医院肝病中心,济南,250021;山东大学附属省立医院肝病中心,济南,250021
基金项目:山东省博士基金资助项目(2006BS03027)
摘    要:目的 观察低分子量肝素对长期摄入高脂饮食所致大鼠非酒精性脂肪性肝炎的干预作用,探讨其机制。方法 雄性SD大鼠40只,随机分为正常对照组(n=10)及模型组(n=10),模型组喂以高脂饮食共8周;其余20只在高脂饮食8周后分为低分子肝素低剂量治疗组(n=10),在继续高脂饲料喂养的基础上,加用低分子量肝素治疗[50IU/(kg·d)];低分子肝素高剂量治疗组(n=10),在继续高脂饲料喂养基础上,加用低分子量肝素治疗[200IU/(kg·d)],共治疗2周。结果 低分子肝素高剂量组[200IU/(kg·d)]在抑制肝脏慢性炎症、防止肝脏脂质堆积方面较模型组有统计学差异,而低剂量组[50IU/(kg·d)]作用不如高剂量组作用明显。结论 低分子量肝素能够抑制肝脏慢性炎症的发生,调节脂质在肝脏中的堆积,有治疗非酒精性脂肪性肝炎的作用,且其作用效果与剂量相关。其作用机制可能是调节血脂,降低血清中TNF-α的水平。

关 键 词:非酒精性脂肪性肝炎  低分子量肝素  甘油三酯  胆固醇  肿瘤坏死因子-α  大鼠  sprague-Dawley
收稿时间:2010-07-16

Low molecular weight heparin attenuating non-alcoholic steatohepatitis caused by high-fat diet in the rat
SUN Lin-lin,SHI Jun,HAO Jing-hua,REN Wan-hua. Low molecular weight heparin attenuating non-alcoholic steatohepatitis caused by high-fat diet in the rat[J]. Journal of Shandong University:Health Sciences, 2010, 48(11): 58-62
Authors:SUN Lin-lin  SHI Jun  HAO Jing-hua  REN Wan-hua
Affiliation:Center for Liver Diseases, Provincial Hospital Affiliated to Shandong University, Jinan 250021, China
Abstract:Objective     To investigated interference of low molecular weight heparin(LMWH) on non-alcoholic steatohepatitis caused by high-fat diet in the rat and study its mechanism. Methods     Male Sprague-Dawley rats(n=40) were randomly divided into the control group(n=10)and the model group(n=10): the model group was given a high fat diet for 8 weeks;  the low dosage treatment group(n=10) and high dosage treatment group(n=10): one received low doses of LMWH [50IU/(kg·d)] and the other received 200IU/(kg·d) for 2 weeks, after 8 weeks of high-fat diet.   Results    Compared with the model group, a high dose of LMWH[200IU/(kg.d)] significantly inhibited chronic inflammation and attenuated lipid deposits in the liver, while a low dose of LMWH was not significant.  Conclusion     LMWH has an excellent therapeutic effect on non-alcoholic fatty liver disease (NAFLD) by inhibiting chronic inflammation and attenuating lipid deposits in the liver, which is closely related to the dosage. Its mechanism may be that LMWH regulates the level of blood fat and decreases the level of TNF α in the serum.
Keywords:Non-alcoholic steatohepatitis   Low molecular weight heparin  Triglyceride  Cholesterol  Tumor necrosis factor-α  Rats, Sprague-Dawley
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