中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Effects of tetrahydroprotoberberines on dopamine D-2 receptors in ventral tegmental area of rat

文献类型:期刊论文

作者Wang, LM; Zhang, XX; Jin, GZ
刊名ACTA PHARMACOLOGICA SINICA
出版日期1997-03
卷号18期号:2页码:143-146
关键词tetrahydroprotoberberines ventral tegmental area dopamine D-2 receptors action potentials apomorphine Sch-23390 haloperidol
ISSN号0253-9756
文献子类Article
英文摘要AIM: To compare the actions of tetrahydroprotoberberines (THPB) on dopa;nine (DA) D-2 receptors in the ventral tegmental area (VTA) of rat. METHODS: Extracellular single unit recording technique was used in iv gallamine-paralyzed rats. RESULTS: Eleven THPB analogs tested completely attenuated the apomorphine (Apo, 20 mu g . kg(-1))-induced inhibition on VTA DA cell firing activity. The OH group on C-2 at THPB was linked with the reversal of Apo-induced inhibition. Their reversal potencies (ED(50), mu g . L(-1)) for D-2 receptors were: THPB-143 (5.6) > SPD (8.5) > Iso (17.0) > THP (33) > THE (48) > THPB-18 (66) > THPB-1 (179) > THPB-19 (408) > THPI-126 (510) > THPB-104 (1019) > THPB-10 (4815). CONCLUSION: Among these 11 THPB, the 2-hydroxyl-THPB (THPB-143) showed the strongest antagonistic action on D-2 receptors.
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
CSCD记录号CSCD:411910
WOS记录号WOS:A1997WM32200013
出版者ACTA PHARMACOLOGICA SINICA
源URL[http://119.78.100.183/handle/2S10ELR8/274920]  
专题药物制剂研究中心
院士及顾问专家
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
Wang, LM,Zhang, XX,Jin, GZ. Effects of tetrahydroprotoberberines on dopamine D-2 receptors in ventral tegmental area of rat[J]. ACTA PHARMACOLOGICA SINICA,1997,18(2):143-146.
APA Wang, LM,Zhang, XX,&Jin, GZ.(1997).Effects of tetrahydroprotoberberines on dopamine D-2 receptors in ventral tegmental area of rat.ACTA PHARMACOLOGICA SINICA,18(2),143-146.
MLA Wang, LM,et al."Effects of tetrahydroprotoberberines on dopamine D-2 receptors in ventral tegmental area of rat".ACTA PHARMACOLOGICA SINICA 18.2(1997):143-146.

入库方式: OAI收割

来源:上海药物研究所

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