Lane R F, Blaha C D, Phillips A G
Brain Res. 1986 Nov 5;397(1):200-4. doi: 10.1016/0006-8993(86)91388-0.
In vivo electrochemical techniques were used to study the effects of the sulfated (CCK8-S) and unsulfated (CCK8-US) forms of the cholecystokinin octapeptide on dopamine (DA) release in the nucleus accumbens. A dose-dependent inhibition of DA release was observed only with CCK8-S. This inhibitory effect was blocked by the CCK receptor antagonist proglumide, and was reversed by systemic injections of apomorphine. Given that apomorphine can hyperpolarize DA neurons, these data indicate that CCK may inhibit the release of DA by a process of depolarization block and suggest a mechanism by which CCK may regulate overactive mesolimbic DA transmission.
采用体内电化学技术研究了胆囊收缩素八肽的硫酸化形式(CCK8-S)和非硫酸化形式(CCK8-US)对伏隔核中多巴胺(DA)释放的影响。仅CCK8-S可观察到DA释放呈剂量依赖性抑制。这种抑制作用被CCK受体拮抗剂丙谷胺阻断,并被阿扑吗啡全身注射所逆转。鉴于阿扑吗啡可使DA神经元超极化,这些数据表明CCK可能通过去极化阻滞过程抑制DA释放,并提示了CCK可能调节过度活跃的中脑边缘DA传递的机制。