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多巴胺D2受体介导的非洲爪蟾视网膜中视杆-视锥细胞耦联的调节

Dopamine D2 receptor-mediated modulation of rod-cone coupling in the Xenopus retina.

作者信息

Krizaj D, Gábriel R, Owen W G, Witkovsky P

机构信息

Department of Physiology and Neuroscience, New York University Medical Center, New York 10016, USA.

出版信息

J Comp Neurol. 1998 Sep 7;398(4):529-38.

Abstract

We studied the responses of rod photoreceptors that were elicited with light flashes or sinusoidally modulated light by using intracellular recording. Dark-adapted Xenopus rod photoreceptors responded to sinusoidally modulated green lights at temporal frequencies between 1 Hz and 4 Hz. In normal Ringer's solution, 57% of the rods tested could follow red lights that were matched for equal rod absorbance to frequencies >5 Hz, indicating an input from red-sensitive cones. Quinpirole (10 microM), a D2 dopamine agonist, increased rod-cone coupling, whereas spiperone (5 microM), a selective D2 antagonist, completely suppressed it. D1 dopamine ligands were without effect. Neurobiotin that was injected into single rods diffused into neighboring rods and cones in quinpirole-treated retinas but only diffused into rods in spiperone-treated retinas. A subpopulation of rods (ca. 10% total rods) received a very strong cone input, which quickened the kinetics of their responses to red flashes and greatly increased the bandpass of their responses to sinusoidally modulated light. Based on electron microscopic examination, which showed that rod-rod and cone-cone gap junctions are common, whereas rod-cone junctions are relatively rare, we postulate that cone signals enter the rod network through a minority of rods with strong cone connections, from which the cone signal is further distributed in the rod network. A semiquantitative model of coupling, based on measures of gap-junction size and distribution and estimates of their conductance and open times, provides support for this assumption. The same network would permit rod signals to reach cones.

摘要

我们通过细胞内记录研究了闪光或正弦调制光引发的视杆光感受器的反应。暗适应的非洲爪蟾视杆光感受器对1赫兹至4赫兹时间频率的正弦调制绿光有反应。在正常林格氏液中,57% 的受试视杆细胞能够跟随与视杆细胞吸光度匹配的红光,频率 >5赫兹,这表明存在来自红敏视锥细胞的输入。D2多巴胺激动剂喹吡罗(10微摩尔)增加了视杆 - 视锥细胞耦合,而选择性D2拮抗剂螺哌隆(5微摩尔)则完全抑制了这种耦合。D1多巴胺配体没有作用。注入单个视杆细胞的神经生物素在喹吡罗处理的视网膜中扩散到相邻的视杆细胞和视锥细胞中,但在螺哌隆处理的视网膜中仅扩散到视杆细胞中。一小部分视杆细胞(约占视杆细胞总数的10%)接受了非常强的视锥细胞输入,这加快了它们对红色闪光反应的动力学,并大大增加了它们对正弦调制光反应的带通。基于电子显微镜检查,结果显示视杆 - 视杆和视锥 - 视锥间隙连接很常见,而视杆 - 视锥连接相对较少,我们推测视锥细胞信号通过少数与视锥细胞有强连接的视杆细胞进入视杆细胞网络,视锥细胞信号从这些视杆细胞进一步在视杆细胞网络中分布。基于间隙连接大小和分布的测量以及它们的电导和开放时间估计的耦合半定量模型为这一假设提供了支持。相同的网络将允许视杆细胞信号到达视锥细胞。

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