Peppe A, Antal A, Tagliati M, Stanzione P, Bodis-Wollner I
Department of Neurology SUNY-HSCB, Brooklyn, New York 11201, USA.
Neurosci Lett. 1998 Feb 27;243(1-3):5-8. doi: 10.1016/s0304-3940(98)00068-8.
We investigated whether or not the D1 agonist, CY 208-243, affects the spatial tuning function of pattern electroretinogram (PERG). Two lightly anaesthetised monkeys were studied before and after CY 208-243 or placebo administration. The results show that the PERG response to 0.5 cycles/degree (c/d; coarse), but not to 2.3 c/d (medium) spatial frequency stimuli disappears following systemic administration of this drug. Since previous results show that D2 blockers attenuate the PERG only above 2.3 c/d, foremost the peak of the normal spatial frequency response function, the current results suggest that dopamine itself, via D1 receptors, may be responsible for the low spatial frequency decline of normal spatial PERG tuning function. We infer that the synergistic activation of D1 and D2 receptors is needed to shape the spatially tuned primate ERG.
我们研究了D1激动剂CY 208-243是否会影响图形视网膜电图(PERG)的空间调谐功能。对两只轻度麻醉的猴子在给予CY 208-243或安慰剂之前和之后进行了研究。结果显示,全身给予该药物后,PERG对0.5周期/度(c/d;粗)空间频率刺激的反应消失,但对2.3 c/d(中等)空间频率刺激的反应未消失。由于先前的结果表明D2阻滞剂仅在高于2.3 c/d时减弱PERG,主要是正常空间频率反应函数的峰值,目前的结果表明多巴胺本身通过D1受体可能是正常空间PERG调谐功能低空间频率下降的原因。我们推断,D1和D2受体的协同激活对于塑造灵长类动物视网膜电图的空间调谐是必需的。