中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Acute effects of huperzine A and tacrine on rat liver

文献类型:期刊论文

作者Ma, XC; Xin, J; Wang, HX; Zhang, T; Tu, ZH
刊名ACTA PHARMACOLOGICA SINICA
出版日期2003-03
卷号24期号:3页码:247-250
关键词cholinesterase inhibitors huperzine A tacrine liver acute toxicity test
ISSN号1671-4083
文献子类Article
英文摘要AIM: To observe the acute effects of huperzine A and tacrine on rat liver. METHODS: Changes of liver coefficient, serum biochemistry, and histopathology were detected after single dose. In vitro cytotoxicity was assessed by determining extracellular and intracellular amount of lactate dehydrogenase in cultured hepatocytes. RESULTS: Both huperzine A and tacrine raised liver coefficient and increased serum aspartate aminotransferase and alanine aminotransferase. Tacrine induced liver histopathologic changes. The acute effects of huperzine A on liver could be redressed by atropine, while effects of tacrine on liver could not. Concentration-dependent in vitro cytotoxicity occurred with tacrine, but not with huperzine A. CONCLUSION: The acute effects of huperzine A on rat liver are not related to hepatotoxicity. The acute effects of tacrine on rat liver are related to hepatotoxicity.
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
CSCD记录号CSCD:1271236
WOS记录号WOS:000181439200010
出版者SHANGHAI INST MATERIA MEDICA
源URL[http://119.78.100.183/handle/2S10ELR8/274255]  
专题药物安全性评价中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Tu, ZH
作者单位1.Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 200031, Peoples R China
2.Fudan Univ, Sch Pharm, Dept Pharmacol, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Ma, XC,Xin, J,Wang, HX,et al. Acute effects of huperzine A and tacrine on rat liver[J]. ACTA PHARMACOLOGICA SINICA,2003,24(3):247-250.
APA Ma, XC,Xin, J,Wang, HX,Zhang, T,&Tu, ZH.(2003).Acute effects of huperzine A and tacrine on rat liver.ACTA PHARMACOLOGICA SINICA,24(3),247-250.
MLA Ma, XC,et al."Acute effects of huperzine A and tacrine on rat liver".ACTA PHARMACOLOGICA SINICA 24.3(2003):247-250.

入库方式: OAI收割

来源:上海药物研究所

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