Guevara B H, Talmaciu R K, Hoffmann I S, Cubeddu L X
Department of Pharmacology, School of Pharmacy, Central University of Venezuela, Caracas, Venezuela.
Brain Res. 1996 Sep 9;733(1):105-7. doi: 10.1016/0006-8993(96)00694-4.
The dopamine (DA)-acetylcholine (ACh) interactions were investigated in dorsal (nucleus caudate, NC) and ventral (olfactory tubercle, OT) striatal regions, of rats and rabbits. Both regions receive a dense dopaminergic innervation and have high ACh concentrations. Brain slices of NC and OT from both animal species were prelabeled with [3H]choline and superfused. In rat and rabbit OT and NC, higher ACh release per pulse was elicited by lower than higher stimulation frequencies; in addition, rabbit tissues released a greater fraction of tissue [3H]transmitter than rat tissues. Blockade of D2 DA-receptors with sulpiride (1 microM), did not modify ACh release in OT and NC of rats and rabbits; suggesting that the lower ACh release observed in rat tissues is not due to an inhibitory dopaminergic tone on cholinergic neurons. Apomorphine (APO), a D2 DA-receptor agonist, inhibited in a concentration-dependent manner the evoked release of ACh from rat and rabbit NC (maximal inhibition = 90%). In rabbit OT, maximal inhibition induced by APO was 49 +/- 2% and in the rat OT, it was 23 +/- 1%. Sulpiride antagonized APO-induced inhibition of ACh release from rat and rabbit NC; however, it failed to prevent APO-induced inhibition in rat OT, and in the rabbit OT reduced it from 47% to 20 +/- 5%. These results indicate differences in the wiring of DA and cholinergic neurons and terminals in dorsal and ventral striatal structures, as well as between rat and rabbit tissues. Cholinergic ventral striatal structures may not receive a direct DA input, and afferent cholinergic nerve terminals (rather than interneurons) predominate in the ventral striatum.
在大鼠和家兔的背侧(尾状核,NC)和腹侧(嗅结节,OT)纹状体区域研究了多巴胺(DA)-乙酰胆碱(ACh)的相互作用。这两个区域都接受密集的多巴胺能神经支配,且乙酰胆碱浓度较高。用[3H]胆碱对两种动物的NC和OT脑片进行预标记并进行灌流。在大鼠和家兔的OT和NC中,较低的刺激频率比较高的刺激频率能引发更高的单次脉冲乙酰胆碱释放;此外,家兔组织释放的组织[3H]递质比例比大鼠组织更高。用舒必利(1微摩尔)阻断D2多巴胺受体,并未改变大鼠和家兔OT及NC中的乙酰胆碱释放;这表明在大鼠组织中观察到的较低乙酰胆碱释放并非由于多巴胺能神经对胆碱能神经元的抑制性调节。阿扑吗啡(APO),一种D2多巴胺受体激动剂,以浓度依赖性方式抑制大鼠和家兔NC中诱发的乙酰胆碱释放(最大抑制率 = 90%)。在家兔OT中,APO诱导的最大抑制率为49±2%,在大鼠OT中为23±1%。舒必利拮抗APO诱导的大鼠和家兔NC中乙酰胆碱释放的抑制作用;然而,它未能阻止APO诱导的大鼠OT中乙酰胆碱释放的抑制,在家兔OT中,它将抑制率从47%降至20±5%。这些结果表明背侧和腹侧纹状体结构中多巴胺能和胆碱能神经元及终末的连接方式存在差异,以及大鼠和家兔组织之间也存在差异。胆碱能腹侧纹状体结构可能不接受直接的多巴胺输入,且传入胆碱能神经终末(而非中间神经元)在腹侧纹状体中占主导地位。