首页> 外文期刊>Stress: the international journal on the biology of stress >Effect of cocaine on striatal dopamine clearance in a rat model of developmental stress and attention-deficit/hyperactivity disorder
【24h】

Effect of cocaine on striatal dopamine clearance in a rat model of developmental stress and attention-deficit/hyperactivity disorder

机译:可卡因对发展应力大鼠模型中纹纹多巴胺间隙的影响及关注缺陷/多动障碍

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Attention-deficit/hyperactivity disorder (ADHD) and developmental stress are considered risk factors for the development of drug abuse. Though the physiological mechanisms underlying this risk are not yet clear, ADHD, developmental stress and drug abuse are known to share underlying disturbances in dopaminergic neurotransmission. Thus, we hypothesized that clearance of cocaine-induced elevations in striatal dopamine would be prolonged in a rat model of ADHD and that this would be further increased by exposure to developmental stress. In the current study, male spontaneously hypertensive rats (SHRs), a well-validated model of ADHD, and control Wistar-Kyoto (WKY) rats were exposed to either standard rearing (nMS) or a maternal separation (MS) paradigm involving removal of the pups from the dam for 180 min/day over 13 days. This produced a 2 x 2 factorial design (SHR/WKY x nMS/MS) with 5-6 rats/group. Striatal clearance of exogenously applied dopamine was measured via in vivo chronoamperometry, and the difference in dopamine uptake parameters before and after cocaine administration was compared between experimental groups. Cocaine, a potent dopamine transporter inhibitor, reliably increased the clearance time of dopamine though no difference in this parameter was found between SHR and WKY strains. However, developmental stress elevated the cocaine-induced increase in time to clear 50% of exogenously applied dopamine (T-50) in SHR but had no effect in WKY rats. These findings suggest that a strain x environment interaction prolongs elevated levels of dopamine thereby potentially increasing the rewarding properties of this drug in SHR.
机译:注意力缺陷/多动障碍(ADHD)和发育压力被认为是滥用药物滥用的风险因素。尽管这种风险的生理机制尚不清楚,但已知ADHD,发育压力和药物滥用缺乏多巴胺能神经递质的潜在干扰。因此,我们假设可卡因诱导的纹状体多巴胺升高的清除将在ADHD的大鼠模型中延长,并且通过暴露于发育应力将进一步增加。在目前的研究中,雄性自发性高血压大鼠(SHR),验证的ADHD良好的模型,以及控制Wistar-kyoto(WKY)大鼠暴露于标准饲养(NMS)或涉及去除的母体分离(MS)范式。大坝的幼崽180分钟/天超过13天。这产生了2×2因子设计(SHR / WKY X NMS / MS),具有5-6只大鼠/组。通过体内计量萌相测量测量外源施用多巴胺的纹状物清除,在实验组之间比较了可卡因施用前后的多巴胺摄取参数的差异。可卡因是一种有效的多巴胺转运蛋白抑制剂,可靠地增加了多巴胺的间隙时间,但在SHR和WKY菌株之间发现该参数没有差异。然而,发育应力升高了可卡因诱导的时间,以清除SHR中的50%的外源施用多巴胺(T-50),但在WKY大鼠没有作用。这些发现表明,应变X环境相互作用延长了多巴胺水平升高,从而可能增加了该药物在SHR中的奖励性质。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号