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多巴胺及其激动剂和拮抗剂对兔视网膜神经节细胞感受野特性的影响。

Effects of dopamine and its agonists and antagonists on the receptive field properties of ganglion cells in the rabbit retina.

作者信息

Jensen R J, Daw N W

出版信息

Neuroscience. 1986 Mar;17(3):837-55. doi: 10.1016/0306-4522(86)90049-7.

Abstract

We investigated the effects of dopamine and its agonists and antagonists on the receptive field properties of ganglion cells in the isolated eyecup preparation of the rabbit. In general, dopamine (20-250 microM) reduced the overall sensitivity of ganglion cells to light stimuli while increasing the spontaneous activity of off-center cells and decreasing the spontaneous activity of on-center cells and on-off directionally selective cells. Neither(-)-apomorphine (8-82 microM) nor the selective D-2 agonist LY 141865 (7-85 microM) mimicked the effects of exogenous dopamine. Instead, both drugs altered the responses of ganglion cells in a manner similar to that of the selective D-1 antagonist SCH 23390. The latter at 4-41 microM: (1) selectively reduced the antagonistic surround responses of off-center cells; (2) changed the sustained excitatory responses of on-center sustained cells to spots of light into sustained inhibitory responses; (3) selectively reduced the leading edge responses of on-off directionally selective cells to moving light stimuli, and (4) decreased the spontaneous activity of off-center cells while increasing the spontaneous activity of on-center cells. The effects of the selective D-2 antagonist S-sulpiride (37-116 microM) on the responses of on-center cells resembled those of exogenous dopamine, while for off-center cells the effects of S-sulpiride were similar to those of (-)-apomorphine and LY 141865. Results were compared with those obtained previously with dopamine antagonists haloperidol, fluphenazine and cis-flupenthixol on ganglion cell responses in the intact rabbit eye. These three drugs were clearly acting at D-1 receptors. The present findings support a physiological role for D-2 receptors in visual processing in the rabbit retina, in particular the hypothesis that endogenous dopamine release is modulated by inhibitory D-2 autoreceptors. They also suggest that one function of dopaminergic neurons may be to modulate the sensitivity of ganglion cells to light stimuli.

摘要

我们研究了多巴胺及其激动剂和拮抗剂对兔离体眼杯标本中神经节细胞感受野特性的影响。一般来说,多巴胺(20 - 250微摩尔)降低了神经节细胞对光刺激的总体敏感性,同时增加了离中心细胞的自发活动,降低了on - center细胞和on - off方向选择性细胞的自发活动。(-)-阿扑吗啡(8 - 82微摩尔)和选择性D - 2激动剂LY 141865(7 - 85微摩尔)均未模拟外源性多巴胺的作用。相反,这两种药物改变神经节细胞反应的方式类似于选择性D - 1拮抗剂SCH 23390。后者在4 - 41微摩尔时:(1)选择性降低离中心细胞的拮抗周边反应;(2)将on - center持续细胞对光点的持续兴奋性反应转变为持续抑制性反应;(3)选择性降低on - off方向选择性细胞对移动光刺激的前沿反应,以及(4)降低离中心细胞的自发活动,同时增加on - center细胞的自发活动。选择性D - 2拮抗剂S - 舒必利(37 - 116微摩尔)对on - center细胞反应的影响类似于外源性多巴胺,而对于离中心细胞,S - 舒必利的作用类似于(-)-阿扑吗啡和LY 141865。将结果与先前在完整兔眼中用多巴胺拮抗剂氟哌啶醇、氟奋乃静和顺式氟哌噻吨对神经节细胞反应所获得的结果进行了比较。这三种药物明显作用于D - 1受体。目前的研究结果支持D - 2受体在兔视网膜视觉处理中的生理作用,特别是内源性多巴胺释放受抑制性D - 2自身受体调节的假说。它们还表明多巴胺能神经元的一个功能可能是调节神经节细胞对光刺激的敏感性。

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