阿替帕美唑
病变
敌手
内分泌学
内科学
生物
神经科学
鹅膏酸
中枢神经系统
医学
病理
受体
血压
心率
美托咪定
作者
Markus Björklund,Jouni Sirviö,Minna Riekkinen,Jukka Sallinen,Mika Scheinin,Paavo Riekkinen
出处
期刊:Neuroscience
[Elsevier]
日期:1999-12-01
卷期号:95 (2): 481-487
被引量:48
标识
DOI:10.1016/s0306-4522(99)00428-5
摘要
We investigated the role of overexpression of alpha2C-adrenoceptors in water maze navigation in mice transgenically manipulated to have a threefold overexpression of the alpha2C-adrenoreceptors. Alpha2C-adrenoreceptors overexpressing mice swam more in the peripheral annulus of the pool and did not find the hidden escape platform as well as the wild type control mice. A subtype-nonselective alpha2-adrenoreceptor antagonist, atipamezole (ATI, 1000 μg/kg, s.c.), fully reversed the deficit in platform finding and search strategy in overexpressing mice. Noradrenaline depletion (−95%) induced by N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP-4) did not impair platform finding of wild type or overexpressing mice. The DSP-4 lesion slightly increased swimming in the peripheral annulus in wild type mice, but not in overexpressing mice. The DSP-4 lesion produced a dissociable effect on the action of atipamezole to improve platform finding and search strategy in overexpressing mice: atipamezole did not alleviate the platform finding deficit in DSP-4 lesioned overexpressing mice, but normalized their abnormal search strategy. These results suggest that the abnormal search pattern and deficit in the accuracy of platform finding are mediated by constitutive activity of overexpressed alpha2C-adrenoreceptors.
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