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Chloride currents in cones modify feedback from horizontal cells to cones in goldfish retina

机译:视锥细胞中的氯离子电流会改变水平细胞对金鱼视网膜视锥细胞的反馈

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In neuronal systems, excitation and inhibition must be well balanced to ensure reliable information transfer. The cone/horizontal cell (HC) interaction in the retina is an example of this. Because natural scenes encompass an enormous intensity range both in temporal and spatial domains, the balance between excitation and inhibition in the outer retina needs to be adaptable. How this is achieved is unknown. Using electrophysiological techniques in the isolated retina of the goldfish, it was found that opening Ca 2+-dependent Cl - channels in recorded cones reduced the size of feedback responses measured in both cones and HCs. Furthermore, we show that cones express Cl - channels that are gated by GABA released from HCs. Similar to activation of I Cl(Ca), opening of these GABA-gated Cl - channels reduced the size of light-induced feedback responses both in cones and HCs. Conversely, application of picrotoxin, a blocker of GABA A and GABA C receptors, had the opposite effect. In addition, reducing GABA release from HCs by blocking GABA transporters also led to an increase in the size of feedback. Because the independent manipulation of Ca 2+-dependent Cl - currents in individual cones yielded results comparable to bath-applied GABA, it was concluded that activation of either Cl - current by itself is sufficient to reduce the size of HC feedback. However, additional effects of GABA on outer retinal processing cannot be excluded. These results can be accounted for by an ephaptic feedback model in which a cone Cl - current shunts the current flow in the synaptic cleft. The Ca 2+-dependent Cl - current might be essential to set the initial balance between the feedforward and the feedback signals active in the cone HC synapse. It prevents that strong feedback from HCs to cones flood the cone with Ca 2+. Modulation of the feedback strength by GABA might play a role during light/dark adaptation, adjusting the amount of negative feedback to the signal to noise ratio of the cone output.
机译:在神经元系统中,必须很好地平衡激发和抑制,以确保可靠的信息传递。视网膜中的锥体/水平细胞(HC)相互作用就是一个例子。由于自然场景在时域和空间域都包含巨大的强度范围,因此需要适应外部视网膜中激发和抑制之间的平衡。如何实现这一点尚不清楚。在孤立的金鱼视网膜中使用电生理技术,发现在记录的视锥中打开Ca 2+依赖性Cl-通道可减少视锥和HCs中测量到的反馈响应的大小。此外,我们表明视锥细胞表达了由HC释放的GABA所控制的Cl-通道。与激活I Cl(Ca)相似,打开这些GABA门控的Cl-通道可减少视锥和HC中光诱导的反馈响应的大小。相反,应用GABA A和GABA C受体阻滞剂pictotoxin具有相反的效果。此外,通过阻止GABA转运蛋白减少HCs中GABA的释放也导致反馈量的增加。由于在单个视锥中独立操纵Ca 2+依赖性Cl-电流可产生与镀浴GABA相当的结果,因此可以得出结论,任一Cl-电流本身的激活都足以减小HC反馈的大小。但是,不能排除GABA对外部视网膜加工的其他影响。这些结果可以由一种神经反馈模型来解释,其中锥体Cl-电流分流了突触间隙中的电流。依赖Ca 2+的Cl-电流对于设置前馈和圆锥HC突触中激活的反馈信号之间的初始平衡可能至关重要。这样可以防止HC强烈反馈到视锥细胞,使Ca 2+淹没视锥细胞。 GABA对反馈强度的调制可能会在明/暗适应过程中发挥作用,从而调整对圆锥输出的信噪比的负反馈量。

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