Popova E, Kupenova P
Department of Physiology, Medical Faculty, Medical University of Sofia, 1431 Sofia, Bulgaria.
Vision Res. 2013 Aug 9;88:22-9. doi: 10.1016/j.visres.2013.06.004. Epub 2013 Jun 25.
The effects of dopamine receptor blockade by sulpiride (D2-class antagonist) and sulpiride plus SCH 23390 (D1-class antagonist) on the V - log I function of the ERG b- and d-waves were investigated in dark adapted frog eyes. We observed that sulpiride enhanced the amplitude of the suprathreshold b- and d-waves in the lower intensity range, where the responses were mediated by rods, but diminished it in the higher intensity range, where the responses were mediated by cones. A similar effect on the b-, but not d-wave amplitude was seen during the perfusion with sulpiride plus SCH 23390. The d-wave amplitude was enhanced over the whole intensity range with the exception of the highest intensities during the combined D1 and D2 receptor blockade. The results obtained indicate that the endogenous dopamine has an overall inhibitory action on the suprathreshold rod-mediated ON and OFF responses, while its action on the cone-mediated responses shows clear ON-OFF asymmetry. It is excitatory upon the ON responses, but inhibitory upon the OFF responses except for those in the highest intensity range. Participation of different types of dopamine receptors (predominantly D2 for the ON versus D1 for the OFF response) is probably responsible for this difference.
在暗适应的蛙眼中,研究了舒必利(D2类拮抗剂)和舒必利加SCH 23390(D1类拮抗剂)对视网膜电图b波和d波的V - log I函数的影响。我们观察到,舒必利在较低强度范围内增强了阈上b波和d波的振幅,此范围内反应由视杆介导,而在较高强度范围内则降低了其振幅,此范围内反应由视锥介导。在灌注舒必利加SCH 23390期间,对b波振幅有类似影响,但对d波振幅无影响。在联合阻断D1和D2受体期间,除最高强度外,d波振幅在整个强度范围内均增强。所得结果表明,内源性多巴胺对阈上视杆介导的开反应和关反应具有总体抑制作用,而其对视锥介导反应的作用表现出明显的开 - 关不对称性。它对开反应具有兴奋性,但对关反应具有抑制性,除了在最高强度范围内的反应。不同类型多巴胺受体(开反应主要为D2,关反应主要为D1)的参与可能是造成这种差异的原因。