Yerkes National Primate Research Center, Emory University, 954 Gatewood Road N.E, Atlanta, GA, 30329, USA.
Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Psychopharmacology (Berl). 2017 Sep;234(17):2607-2617. doi: 10.1007/s00213-017-4653-2. Epub 2017 Jun 5.
Accumulating evidence shows that the serotonergic system plays a major role in psychostimulant abuse through its interactions with the dopaminergic system. Studies indicate that serotonin 5-HT receptors are one of the main classes of receptors involved in mediating the influence of serotonin in drug abuse.
The aim of the present study was to evaluate the effects of the selective serotonin 5-HT receptor agonist WAY163909 on the behavioral neuropharmacology of cocaine and methamphetamine in adult rhesus macaques.
Cocaine or methamphetamine self-administration and reinstatement were evaluated under second-order and fixed-ratio schedules of reinforcement, respectively. Cocaine- and methamphetamine-induced increases in dopamine were assessed through in vivo microdialysis targeting the nucleus accumbens.
Pretreatment with WAY163909 dose-dependently attenuated cocaine and methamphetamine self-administration and drug-induced reinstatement of extinguished behavior previously maintained by cocaine or methamphetamine delivery. In an additional experiment, WAY163909 induced a dose-dependent attenuation of cocaine- or methamphetamine-induced dopamine overflow in the nucleus accumbens.
Our data indicate that selective 5-HT receptor activation decreases drug intake and drug-seeking behavior in nonhuman primate models of psychostimulant abuse through neurochemical mechanisms involved in the modulation of mesolimbic dopamine.
越来越多的证据表明,5-羟色胺能系统通过与多巴胺能系统相互作用,在精神兴奋剂滥用中起着重要作用。研究表明,5-羟色胺 5-HT 受体是介导 5-羟色胺在药物滥用中影响的主要受体之一。
本研究旨在评估选择性 5-羟色胺受体激动剂 WAY163909 对成年恒河猴可卡因和甲基苯丙胺行为神经药理学的影响。
通过第二阶和固定比率强化程序分别评估可卡因或甲基苯丙胺的自我给药和复吸。通过针对伏隔核的体内微透析评估可卡因和甲基苯丙胺诱导的多巴胺增加。
WAY163909 预处理剂量依赖性地减弱了可卡因和甲基苯丙胺的自我给药以及先前由可卡因或甲基苯丙胺给药维持的行为消退后的药物复吸。在一项额外的实验中,WAY163909 诱导了伏隔核中可卡因或甲基苯丙胺诱导的多巴胺溢出的剂量依赖性减弱。
我们的数据表明,选择性 5-HT 受体激活通过调节中脑边缘多巴胺,减少了非人类灵长类动物滥用精神兴奋剂模型中的药物摄入和觅药行为。