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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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摘要

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 Ca2+-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 ICl(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 GABAA and GABAC 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 Ca2+-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 Ca2+-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 Ca2+. 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:在神经系统中,必须很好地平衡激励和抑制,以确保可靠的信息传输。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,因此需要调整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。使用电生理技术在孤立的金鱼视网膜中,发现在记录的视锥中打开依赖于Ca 2 + 的Cl -通道可以减小在两个视锥中测量到的反馈响应的大小。视锥细胞和HCs。此外,我们表明视锥细胞表达了由HC释放的GABA控制的Cl -通道。与激活ICl(Ca)相似,这些GABA门控的Cl -通道的打开减少了视锥细胞和HCs中光诱导的反馈响应的大小。相反,应用GABAA和GABAC受体阻滞剂微毒素具有相反的效果。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增加。因为独立操纵Ca 2 + 依赖的Cl -电流在单个锥体中产生的结果可与镀浴的GABA相当,所以可以得出结论,激活任一Cl 电流本身足以减小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,在该模型中,圆锥Cl -电流将突触裂隙中的电流分流。 Ca 2 + 依赖的Cl -电流对于设置前馈和锥体HC突触中激活的反馈信号之间的初始平衡可能是必不可少的。这样可以防止HC强烈反馈到视锥,并用Ca 2 + 淹没视锥。 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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