Therapeutic effects of compound glycyrrhizin liposome on rats with nonalcoholic steatohepatitis.
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摘要: 目的观察复方甘草甜素脂质体对大鼠非酒精性脂肪性肝炎(NASH)的干预作用。方法SD雄性大鼠35只随机分为4组,模型组、复方甘草甜素对照组和复方甘草甜素脂质体治疗组各10只,给予高脂饲料喂养,另设5只普通饲料喂养大鼠作为正常组。8周后开始腹腔内注射药物干预,16周后处死全部实验大鼠。全自动生化分析仪检测血清ALT、AST及GGT水平,参照2006年2月份的NAFLD诊疗指南中脂肪肝分度和炎症分级(NASH-F(0-4)G(0-3))的组织病理学标准进行量化计分。结果与模型组相比,治疗组血清AST水平明显下降(P<0.05),血清GGT水平与肝组织炎症计分均显著下降(P<0.01);与对照组比较,治疗组肝组织炎症计分及血清GGT水平均显著降低(P>0.01)。结论复方甘草甜素脂质体对高脂饮食诱发的大鼠脂肪性肝炎有一定的防治作用。Abstract: Objective To investigate the therapeutic effects of compound glycyrrhizin liposome on rats with nonalcoholic steatohepatitis.Methods 35 male SD rats were randomly divided into 4 groups: the model group (n=10) 、compound glycyrrhizin control group (n=10) and compound glycyrrhizin liposome treated group (n=10) all were fed with fat-rich diet, and the normal group (n=5) with normal diet.Drug was given to each group after 8th week, all rats were sacrificed at 16 th week.The serum levels of ALT、AST and GGT were measured with auto-biochemistry instrument.The hepatic histologic scores on fat-liver and inflammation of NASH were done according to the guidelines of the diagnosis and treatment of NAFLD in February 2006.Results Compared with model group, the blood-serum levels of AST reduced significantly in treated group (P<0.05) , the blood-serum levels of GGT and hepatic histologic scores on inflammation of NASH both reduced remarkably in treated group (P<0.01) ;Compared with control group, the hepatic histologic scores on inflammation of NASH and the blood-serum levels of GGT both reduced remarkably in treated group (P<0.01) .Conclusion Compound glycyrrhizin liposome is effective in treatment of steatohepatitic rats induced by fat-rich diet.
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Key words:
- Nonalcholic steatohepatitis /
- compound glycyrrhizin /
- liposome /
- fat-rich diet
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[1]方继伟, 范建高.非酒精性脂肪性肝病的治疗现状[J].中华肝脏病杂志, 2003, 11 (2) ∶120-122. [2]Juergen S, Peter R G.Treatment of nonalcoholic fatty liverdisease[J].World J Gastroenterol, 2006, 12 (14) ∶2161-2167. [3]刘协, 顾呈华, 胡启之, 等.甘草甜素脂质体对小鼠急性酒精性肝损伤的保护作用[J].中国临床康复, 2004, 8 (36) ∶8260-8261。 [4]马中春.甘草甜素对四氯化碳诱发大鼠肝脏损伤的作用及其机制[J].毒理学杂志, 2005, 19 (3) ∶250-251. [5]中华医学会肝脏病学分会脂肪肝和酒精性肝病学组.非酒精性脂肪性肝病诊疗指南[J].中华肝脏病杂志, 2006, 14 (3) ∶161-163. [6]李祖惠, 杨辉.脂质体药物研究进展[J].中国药业, 2005, 14 (10) ∶75-76.
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