中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Effects of tetrahydroprotoberberines on dopamine release and 3,4-dihydroxyphenylacetic acid level in corpus striatum measured by in vivo voltammetry

文献类型:期刊论文

作者Huang, K X; Sun, B C; Gonon, F G; Jin, G Z
刊名Zhongguo yao li xue bao = Acta pharmacologica Sinica
出版日期1991-01
卷号12期号:1页码:32-6
ISSN号0253-9756
文献子类Article
英文摘要The extracellular (DA) and 3,4-dihydroxyphenylacetic acid (DOPAC) in rat striatum were measured by in vivo voltammetry to elucidate the effects of 3 tetrahydroprotoberberines on DA neurotransmission. l-tetrahydropalmatine (l-THP, 2 mg.kg-1) or l-stepholidine (l-SPD, 0.5 mg.kg-1) iv increased the striatal DA release by 225% and 233%, respectively; and l-SPD increased the DOPAC level by 70%. Moreover, the enantiomer d-THP (2 mg.kg-1) increased the DA release by 97%, and a large dose of d-THP (20 mg.kg-1) dramatically increased the extracellular DA by 1456% while it slightly elevated the DOPAC level by 123%. These results support the previous ideas that l-SPD and l-THP can block DA receptors and d-THP can deplete neuronal DA.
语种中文
源URL[http://119.78.100.183/handle/2S10ELR8/266297]  
专题中国科学院上海药物研究所
作者单位Shanghai Institute of Materia Medica, Chinese Academy of Sciences
推荐引用方式
GB/T 7714
Huang, K X,Sun, B C,Gonon, F G,et al. Effects of tetrahydroprotoberberines on dopamine release and 3,4-dihydroxyphenylacetic acid level in corpus striatum measured by in vivo voltammetry[J]. Zhongguo yao li xue bao = Acta pharmacologica Sinica,1991,12(1):32-6.
APA Huang, K X,Sun, B C,Gonon, F G,&Jin, G Z.(1991).Effects of tetrahydroprotoberberines on dopamine release and 3,4-dihydroxyphenylacetic acid level in corpus striatum measured by in vivo voltammetry.Zhongguo yao li xue bao = Acta pharmacologica Sinica,12(1),32-6.
MLA Huang, K X,et al."Effects of tetrahydroprotoberberines on dopamine release and 3,4-dihydroxyphenylacetic acid level in corpus striatum measured by in vivo voltammetry".Zhongguo yao li xue bao = Acta pharmacologica Sinica 12.1(1991):32-6.

入库方式: OAI收割

来源:上海药物研究所

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