Matthews R T, German D C
Eur J Pharmacol. 1986 Jan 14;120(1):87-93. doi: 10.1016/0014-2999(86)90644-8.
The microiontophoretic application of dopamine onto neurons in the substantia nigra of rats increased the spontaneous activity of zona reticulata (ZR) neurons but decreased the activity of zone compacta (ZC) neurons. The systemic administration of the dopamine antagonists, haloperidol and cis-flupentixol, blocked the dopamine effects. However, haloperidol was more potent on ZC neurons that on ZR neurons whereas cis-flupentixol was of comparable potency on ZC and ZR neurons. In addition, microiontophoretic application of a cyclic adenosine monophosphate analog was found to mimic the effects of dopamine on ZR neurons, but not on ZC neurons. Taken together with receptor binding studies on the relative affinities of haloperidol and cis-flupentixol for various dopamine receptor subtypes, these data suggest that the excitatory effect of dopamine on ZR neurons is mediated by a D-1 type receptor whereas its inhibitory effect on the ZC dopaminergic neuron is mediated by a D-2 type receptor.
向大鼠黑质中的神经元微量离子电泳施加多巴胺,可增加网状带(ZR)神经元的自发活动,但会降低致密带(ZC)神经元的活动。多巴胺拮抗剂氟哌啶醇和顺式氟奋乃静的全身给药可阻断多巴胺的作用。然而,氟哌啶醇对ZC神经元的作用比对ZR神经元更强,而顺式氟奋乃静对ZC和ZR神经元的作用效力相当。此外,发现微量离子电泳施加环磷酸腺苷类似物可模拟多巴胺对ZR神经元的作用,但对ZC神经元无此作用。结合关于氟哌啶醇和顺式氟奋乃静对各种多巴胺受体亚型的相对亲和力的受体结合研究,这些数据表明多巴胺对ZR神经元的兴奋作用由D-1型受体介导,而其对ZC多巴胺能神经元的抑制作用由D-2型受体介导。