Pearce R A
Department of Anesthesiology, University of Wisconsin, Madison 53706.
Neuron. 1993 Feb;10(2):189-200. doi: 10.1016/0896-6273(93)90310-n.
The gamma-aminobutyric acid(A) (GABAA) receptor is a ligand-gated ionophore involved in synaptic inhibition. Biochemical and molecular biological studies indicate that considerable receptor heterogeneity exists, but physiological differences between inhibitory GABAA synaptic responses have not been identified in the brain. The present report describes two anatomically segregated GABAA-mediated synaptic currents in the hippocampal CA1 region that have distinct physiological, pharmacological, and functional properties. GABAA,fast enters at or near the cell body, decays rapidly (3-8 ms), is blocked by furosemide, and rapidly curtails the excitatory response. GABAA,slow enters far from the cell body, decays slowly (30-70 ms), is not blocked by furosemide, and underlies the conventionally recognized early inhibitory postsynaptic potential. The receptors producing these responses may represent subtypes of the GABAA receptor.
γ-氨基丁酸A(GABAA)受体是一种参与突触抑制的配体门控离子通道。生化和分子生物学研究表明,该受体存在相当大的异质性,但在大脑中尚未确定抑制性GABAA突触反应之间的生理差异。本报告描述了海马CA1区两种在解剖学上分离的GABAA介导的突触电流,它们具有不同的生理、药理和功能特性。快速型GABAA电流在细胞体处或其附近快速进入,迅速衰减(3 - 8毫秒),被速尿阻断,并迅速抑制兴奋性反应。慢型GABAA电流在远离细胞体的位置进入,衰减缓慢(30 - 70毫秒),不被速尿阻断,是传统上公认的早期抑制性突触后电位的基础。产生这些反应的受体可能代表GABAA受体的亚型。