Kuczenski R, Segal D S, Manley L D
Department of Psychiatry, University of California, San Diego, La Jolla 92093.
J Neurochem. 1990 May;54(5):1492-9. doi: 10.1111/j.1471-4159.1990.tb01196.x.
Amphetamine facilitates the release of dopamine from nerve terminals, but the mechanisms underlying this effect have not been fully delineated. The present experiments were designed to test the extent to which amphetamine-induced dopamine release is dependent on impulse flow and autoreceptor function in dopaminergic neurons. Rats were pretreated with a low dose of apomorphine (0.05 mg/kg) to inhibit dopamine neuronal activity, and the striatal dopaminergic response to amphetamine (0.5 mg/kg) was assessed by in vivo dialysis in freely moving animals. Consistent with previous results, apomorphine alone substantially decreased, whereas amphetamine increased, striatal dialysate dopamine concentrations. However, whereas apomorphine pretreatment decreased the locomotor response to amphetamine, the amphetamine-induced increase in dialysate dopamine was unaffected. These results indicate that amphetamine-facilitated dopamine release is independent of neuronal firing and autoreceptor regulation, consistent with the putative accelerative exchange-diffusion mechanism of amphetamine-induced dopamine release. Other possible mechanisms underlying the inhibitory effects of apomorphine on amphetamine locomotor activation are discussed.
安非他命可促进神经末梢释放多巴胺,但其作用机制尚未完全阐明。本实验旨在测试安非他命诱导的多巴胺释放依赖于多巴胺能神经元冲动流和自身受体功能的程度。给大鼠预先注射低剂量阿扑吗啡(0.05mg/kg)以抑制多巴胺神经元活动,并通过在自由活动动物体内进行透析来评估纹状体对安非他命(0.5mg/kg)的多巴胺能反应。与先前结果一致,单独使用阿扑吗啡可显著降低,而安非他命可增加纹状体透析液中的多巴胺浓度。然而,尽管阿扑吗啡预处理降低了对安非他命的运动反应,但安非他命诱导的透析液多巴胺增加并未受到影响。这些结果表明,安非他命促进的多巴胺释放与神经元放电和自身受体调节无关,这与安非他命诱导多巴胺释放的假定加速交换扩散机制一致。还讨论了阿扑吗啡对安非他命运动激活抑制作用的其他可能机制。