中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Ginkgolide A, B, and huperzine A inhibit nitric oxide-induced neurotoxicity

文献类型:期刊论文

作者Zhao, HW; Li, XY
刊名INTERNATIONAL IMMUNOPHARMACOLOGY
出版日期2002-10
卷号2期号:11页码:1551-1556
关键词ginkgolides huperzine a nitric oxide cell growth apoptosis SK-N-SH cells
ISSN号1567-5769
DOI10.1016/S1567-5769(02)00093-0
文献子类Article
英文摘要Nitric oxide (NO) is believed to play important roles in neuronal degeneration. In this study, the effects of NO on cell growth and apoptosis have been examined in human neuroblastoma cell line SK-N-SH. Sodium nitroprusside (SNP), a NO donor, was found to significantly inhibit cell growth and to induce apoptosis. The inhibitory and apoptotic activities of SNP followed a dose- and time-dependent manner. Ginkgolide A, B (GA, 13), and huperzine A (Hup A), the three compounds isolated from Chinese herbs, blocked the inhibition of cell growth and apoptosis induced by SNP. The results suggest that inhibition of NO-induced neurotoxicity may be one mechanism of the above three therapeutic agents in neurodegenerative diseases. (C) 2002 Elsevier Science B.V All rights reserved.
WOS关键词BILOBA EXTRACT EGB-761 ; CELL-DEATH ; IN-VITRO ; MECHANISMS ; CYTOKINES ; APOPTOSIS ; GROWTH ; INVOLVEMENT ; TOXICITY ; RESCUES
WOS研究方向Immunology ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000179095700005
出版者ELSEVIER SCIENCE BV
源URL[http://119.78.100.183/handle/2S10ELR8/274326]  
专题中国科学院上海药物研究所
通讯作者Zhao, HW
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China
推荐引用方式
GB/T 7714
Zhao, HW,Li, XY. Ginkgolide A, B, and huperzine A inhibit nitric oxide-induced neurotoxicity[J]. INTERNATIONAL IMMUNOPHARMACOLOGY,2002,2(11):1551-1556.
APA Zhao, HW,&Li, XY.(2002).Ginkgolide A, B, and huperzine A inhibit nitric oxide-induced neurotoxicity.INTERNATIONAL IMMUNOPHARMACOLOGY,2(11),1551-1556.
MLA Zhao, HW,et al."Ginkgolide A, B, and huperzine A inhibit nitric oxide-induced neurotoxicity".INTERNATIONAL IMMUNOPHARMACOLOGY 2.11(2002):1551-1556.

入库方式: OAI收割

来源:上海药物研究所

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