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食品研究与开发:2019,40(8):184-187
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桧木纯露解酒护肝作用的实验研究
(广西中医药大学,广西南宁530001)
Study on the Effect of Guimu Chunlu on Antialcoholism and Liver Protection in Mice
(Guangxi University of Traditional Chinese Medicine,Nanning 530001,Guangxi,China)
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投稿时间:2018-08-26    
中文摘要: 为考察桧木纯露的解酒防醉效果及其对小鼠酒精性肝损伤的保护作用,将100 只雄性小鼠随机分为模型组、阳性药对照组(0.15 mL/10 g)、桧木纯露高、中、低剂量组(0.2、0.15、0.1 mL/10 g)。通过灌胃各组小鼠56 度红星二锅头(0.15 mL/10 g),观察其醉酒潜伏期和醒酒时间研究其防醉与解酒活性。同时各组小鼠灌胃相应药物连续14 d,测定小鼠血清中天门冬氨酸氨基转移酶(aspartate aminotransferase,AST)、丙氨酸氨基转移酶(alanine aminotransferase,ALT)及肝组织中丙二醛(malondialdehyde,MDA)、超氧化物歧化酶(superoxide dismutase,SOD)水平,并计算肝脏脏器系数。结果表明,各给药组小鼠的醉酒潜伏期较模型组小鼠相比延长且醒酒时间缩短(P<0.05 或P<0.01),桧木纯露组小鼠血清AST 及ALT 活性下降,肝组织中SOD 水平升高MDA 水平降低(P<0.05 或P<0.01),肝脏系数降低(P<0.05 或P<0.01)。说明桧木纯露具有防醉解酒作用,可增强酒精中毒小鼠的抗氧化能力,对小鼠酒精性肝损伤具有一定的保护作用。
中文关键词: 桧木纯露  解酒  防醉  护肝  抗氧化
Abstract:In order to investigate the effect of Guimu Chunlu(GMCL)on antialcoholism and liver protection in mice,100 male mice were randomly divided into model group,positive drug control group(0.15 mL/10 g),GMCL high,medium and low dose groups(0.2,0.15,0.1 mL/10 g).The mice were administrated 0.15 mL/10 g ethanol,the latent time of drunkenness and the durative time of drunkenness were calculated in all groups.Mice were administrated the related drugs for 14 d,the activities of serum ALT(aspartate aminotransferase)and AST(alanine aminotransferase),the content of MDA(malondialdehyde)and SOD(superoxide dismutase)in liver were measured.And the liver index was calculated.The results showed that GMCL could significantly(P<0.05 or P<0.01)postpone the tolerance time of mice to the alcohol,and shorten the duration of drunkenness obviously. GMCL could markedly decrease the activities of AST and ALT,the level of MDA and liver index,increase the activities of SOD (P<0.05 or P<0.01). It showed that GMCL had beneficial effects on preventing drunkenness and relieving alcoholism.It could reduce liver injury induced by ethanol in mice.
文章编号:201908032     中图分类号:    文献标志码:
基金项目:广西中医药大学2017年国家级大学生创新创业训练计划(201710600019);广西高校中药药理重点实验室(广西中医药大学)自主研究课题(J1700303);广西壮瑶药重点实验室(桂科基字[2014]32 号);壮瑶药协同创新中心(桂教科研[2013]20 号);广西重点学科(壮药学)(桂教科研[2013]16 号)
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