Gorell J M, Czarnecki B, Hubbell S
Life Sci. 1986 Jun 16;38(24):2247-54. doi: 10.1016/0024-3205(86)90577-1.
Rat striatal slices prelabelled with [3H]choline were superfused with dopamine D-1 and D-2 agonists and antagonists, separately and in combination, during measurement of [3H]acetylcholine (ACh) release. SKF38393 (D-1 agonist), 10(-7)-10(-4) M, and SCH23390 (D-1 antagonist), 10(-7)-10(-5) M, produced a dose-dependent increase in [3H]ACh release when given separately. The increased [3H]ACh release induced by either drug could not be attenuated by sufficient L-sulpiride to block D-2 receptors. Yet both SKF38393, 10(-6)-10(-5) M, and SCH23390, 10(-6)-10(-5) M, were able to partially or fully overcome the [3H]ACh release-depressant effect of cosuperfused LY171555 (D-2 agonist), 10(-6) M. This suggests that a functional antagonism regarding striatal ACh release exists between D-1 and D-2 dopaminergic receptor-mediated mechanisms, but that D-1 modulation of local ACh release does not occur at the level of the recognition site of the striatal D-2 receptor. Finally, although attenuation of the increased release of striatal [3H]ACh induced by 10(-5) M SCH23390 by SKF38393 was seen, it is possible that such functional antagonism is not mediated by exclusively D-1 dopaminergic means.
在用[3H]胆碱预标记的大鼠纹状体切片中,在测量[3H]乙酰胆碱(ACh)释放期间,分别或联合用多巴胺D-1和D-2激动剂及拮抗剂进行灌流。单独给予10(-7)-10(-4)M的SKF38393(D-1激动剂)和10(-7)-10(-5)M的SCH23390(D-1拮抗剂)时,[3H]ACh释放呈剂量依赖性增加。两种药物所诱导的[3H]ACh释放增加均不能被足以阻断D-2受体的L-舒必利所减弱。然而,10(-6)-10(-5)M的SKF38393和10(-6)-10(-5)M的SCH23390都能够部分或完全克服共灌流的10(-6)M LY171555(D-2激动剂)对[3H]ACh释放的抑制作用。这表明在D-1和D-2多巴胺能受体介导的机制之间存在关于纹状体ACh释放的功能性拮抗作用,但纹状体D-2受体识别位点水平上不存在D-1对局部ACh释放的调节作用。最后,虽然观察到SKF38393可减弱10(-5)M SCH23390所诱导的纹状体[3H]ACh释放增加,但这种功能性拮抗作用可能并非仅由D-1多巴胺能方式介导。