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作 者:高敬国[1]
出 处:《中药药理与临床》2016年第2期27-31,共5页Pharmacology and Clinics of Chinese Materia Medica
摘 要:目的:研究熊果酸(Ursolic Acid,UA)对非酒精性脂肪肝大鼠肝脏的保护作用及其机制。方法:取120只大鼠随机分为正常对照组、模型组,熊果酸(10、20、40mg/kg)组和多烯磷脂酰胆碱(64mg/kg)组;采用高脂饲料喂养8周的方法制备非酒精性脂肪肝大鼠模型;造模过程灌胃给药,每天1次。8周后,计算肝脏指数;测定血清中转氨酶(ALT、AST)、胆碱酯酶(CHE)含量以及血脂(TC、TG、LDL-C、HDL-C)和游离脂肪酸(FFA)水平;测定肝脏组织中TC和TG含量;ELISA法测定血清中炎症细胞因子(TNF-α、IL-6)水平;HE染色法观察肝脏组织结构形态学变化并行肝组织脂肪变性分级。结果:与模型组比较,熊果酸(20、40mg/kg)组大鼠肝脏指数显著降低,血清中ALT、AST、CHE含量和TC、TG、LDL-C、FFA水平显著降低,肝组织中TC和TG含量显著降低,血清中TNF-α、IL-6水平显著降低;熊果酸40mg/kg组HDL-C含量显著升高;熊果酸治疗组大鼠肝脏组织病变以及肝细胞脂肪性病变、炎症病变均明显改善,以熊果酸40mg/kg组效果最为显著,熊果酸(20、40mg/kg)组脂肪性病变和炎症病变程度等级较模型组均显著降低。结论:熊果酸对非酒精性脂肪肝大鼠肝脏组织具有保护作用;作用机制可能与熊果酸能够有效调节血脂,降低炎症因子水平、抑制炎症反应有关。Objective: To investigate the protective effects and mechanism of Ursolic Acid( UA) on nonalcoholic fatty liver in rats. Methods: One hundred and twenty experimental rats were randomly devided into six groups: normal control group,model group,UA( 10,20,40 mg / kg)groups and Polyene phosphatidylcholine 64 mg / kg group. The model rats were made by feeding with high fat dier for eightweeks,and the drugs were given by intragastric administration at the same time,once a day. Eight weeks later,the hepatic index were detected; the content of ALT,AST,CHE,TC,TG,LDL-C,HDL-C and FFA in serum were determined; the level of TNF-α,IL-6 in serum were also determined by ELISA; the content of TC and TG in hepatic tissue were detected; the histopathological changes of hepatic tissue was observed by HE staining,and the fatty lesions rating was evaluated. Results: Compared with the model group,the hepatic index of UA( 20,40 mg / kg) treated groups were significantly decreased; the content of ALT,AST,CHE,TC,TG,LDL-C,FFA in serum and the content of TC,TG in hepatic tissue of UA( 20,40 mg / kg) treated groups were significantly decresed,the content of HDL-C in UA 40 mg / kg treated group was significantly increased; the level of TNF-α,IL-6 were significantly decreased; the hepatic tissue histopathological changes of UA treated groups were significantly improved,especially the UA 40 mg / kg treated group; the fatty lesions rating of UA( 20,40 mg / kg) treated groups were significantly decreased( P 〈 0. 05). Conclusion: UA had protective effects on nonalcoholic fatty liver in rats; which perhaps related to its effects of reducing cholesterol,lowering inflammatory cytokines levels.
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