Gorell J M, Czarnecki B
Life Sci. 1986 Jun 16;38(24):2239-46. doi: 10.1016/0024-3205(86)90576-x.
This study was done to provide pharmacologic evidence for the location of those striatal dopamine D-1 and D-2 receptors that participate in the regulation of local acetylcholine (ACh) release. Striatal tissue slices from adult male Sprague-Dawley rats were preloaded with [3H]choline and superfused in separate experiments with buffer containing either: a D-2-specific agonist (LY141865 or LY171555), a D-2 specific antagonist (L-sulpiride), a D-1 specific agonist (SKF38393), or a D-1 antagonist (SCH23390), in the presence or absence of tetrodotoxin (TTX), used to block interneuronal activity. With either D-2 agonist there was a dose-dependent decrease in K+-stimulated [3H]ACh release, maximally at 5 X 10(-7)-10(-6) M [agonist] and to the same extent with each drug. Both SKF38393 and SCH23390 increased [3H]ACh release at tested concentrations of these agents. Results were unchanged when any of the drugs used was superfused in the presence of TTX, 5 X 10(-7) M. These data are consistent with the hypothesis that populations of striatal D-1 and D-2 receptors exist on local cholinergic neurons, where they regulate ACh release. Alternative interpretations are discussed.
本研究旨在为参与调节局部乙酰胆碱(ACh)释放的纹状体多巴胺D-1和D-2受体的定位提供药理学证据。取成年雄性Sprague-Dawley大鼠的纹状体组织切片,预先用[3H]胆碱加载,然后在单独的实验中用含有以下物质的缓冲液进行灌流:一种D-2特异性激动剂(LY141865或LY171555)、一种D-2特异性拮抗剂(L-舒必利)、一种D-1特异性激动剂(SKF38393)或一种D-1拮抗剂(SCH23390),同时存在或不存在用于阻断中间神经元活动的河豚毒素(TTX)。使用任何一种D-2激动剂时,K+刺激的[3H]ACh释放均呈剂量依赖性降低,在[激动剂]浓度为5×10(-7)-10(-6)M时达到最大程度,且每种药物降低的程度相同。在这些药物的测试浓度下,SKF38393和SCH23390均增加了[3H]ACh释放。当所用的任何一种药物在5×10(-7)M的TTX存在下进行灌流时,结果不变。这些数据与以下假设一致:纹状体D-1和D-2受体群体存在于局部胆碱能神经元上,在那里它们调节ACh释放。文中还讨论了其他解释。