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Mastoparan activation of dopamine-modulated K+ channels on rat striatal neurons.

作者信息

Greif G J, Lin Y J, Freedman J E

机构信息

Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.

出版信息

Neuroreport. 1995 Jun 19;6(9):1277-80. doi: 10.1097/00001756-199506090-00012.

Abstract

Coupling mechanisms between a D2-like dopamine receptor and an 85 pS K+ channel on freshly dissociated rat caudate-putamen neurons were studied using cell-attached patch-clamp electrophysiology. Channel currents were observed in the absence of dopamine receptor agonists when mastoparan, an activator of certain guanyl nucleotide binding proteins (G-proteins), was applied via the patch pipette. Channel current-voltage relationships and open probabilities observed with mastoparan were indistinguishable from those obtained with dopaminergic agonists. Alamethicin, which mimics the membrane-perturbing but not the G-protein activating properties of mastoparan, did not activate the channel, suggesting that non-specific effects of mastoparan were unlikely to account for this effect. Our results indicate that coupling between the D2 dopamine receptor and this K+ channel may involve a mastoparan-sensitive G-protein.

摘要

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