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γ-氨基丁酸增强鲤鱼L型水平细胞对短波长敏感视锥细胞的输入,并减少对红色视锥细胞的输入。

GABA enhances short wavelength-sensitive cone input and reduces red cone input to carp L-type horizontal cells.

作者信息

Xu H, Yang X

机构信息

Shanghai Institute of Physiology and Key Laboratory of Neurobiology, Chinese Academy of Sciences, China.

出版信息

Brain Res Bull. 2000 Apr;51(6):493-7. doi: 10.1016/s0361-9230(99)00272-5.

Abstract

Light responses of cone-driven horizontal cells were recorded intracellularly in the isolated superfused carp retina and the effects of gamma-aminobutyric acid (GABA) on signals from red-sensitive (R-) and short-wavelength-sensitive (S-) cones (green cones and/or blue cones) were studied. In the presence of a bright red (694 nm) background light, which substantially suppressed signal from R-cones, the responses of L-type horizontal cells (L-HCs) to 532-nm flashes, predominantly driven by the S-cone input, were potentiated by application of GABA. In contrast, the responses of these cells to 694-nm flashes driven by the R-cone input, were suppressed, when signal from S-cones was suppressed by a bright 532-nm background light. Both the effects could be reversed by co-application of bicuculline, suggesting the involvement of GABA(A) receptors. It was unlikely that the potentiation by GABA of the S-cone driven responses of the L-HCs was mediated by actions of GABA on the cone photoreceptors. The dual action of GABA persisted in the dopamine-depleted retina, indicating no involvement of the dopaminergic interplexiform cells. We speculate that this dual action may be partially due to differential modulation by GABA of different postsynaptic mechanisms respectively mediating signal transfer from R-cones and S-cones to L-HCs.

摘要

在分离的灌注鲤鱼视网膜中,细胞内记录了视锥驱动的水平细胞的光反应,并研究了γ-氨基丁酸(GABA)对来自红色敏感(R-)和短波长敏感(S-)视锥(绿色视锥和/或蓝色视锥)信号的影响。在明亮的红色(694nm)背景光存在下,该背景光显著抑制了R-视锥的信号,L型水平细胞(L-HCs)对主要由S-视锥输入驱动的532nm闪光的反应,在应用GABA后增强。相反,当532nm明亮背景光抑制S-视锥信号时,这些细胞对由R-视锥输入驱动的694nm闪光的反应被抑制。这两种效应均可通过共同应用荷包牡丹碱而逆转,提示涉及GABA(A)受体。GABA对L-HCs的S-视锥驱动反应的增强不太可能是由GABA对视锥光感受器的作用介导的。GABA的双重作用在多巴胺耗尽的视网膜中持续存在,表明多巴胺能网间细胞不参与其中。我们推测,这种双重作用可能部分是由于GABA对分别介导从R-视锥和S-视锥到L-HCs信号传递的不同突触后机制的差异调节。

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