首页> 美国卫生研究院文献>other >Effects of nicotinic acetylcholine receptor agonists on cognition in rhesus monkeys with a chronic cocaine self-administration history
【2h】

Effects of nicotinic acetylcholine receptor agonists on cognition in rhesus monkeys with a chronic cocaine self-administration history

机译:烟碱乙酰胆碱受体激动剂对慢性可卡因自我管理历史恒河猴认知的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cocaine use is associated with impaired cognitive function, which may negatively impact treatment outcomes. One pharmacological strategy to improve cognition involves nicotinic acetylcholine receptor (nAChR) stimulation. However, the effects of chronic cocaine exposure on nAChR distribution and function have not been characterized. Thus, one goal of this study was to examine nAChR availability in rhesus monkeys with an extensive cocaine self-administration history (n = 4; ~6 years, mean intake, 1463 mg/kg) compared to age-matched cocaine-naive control monkeys (n = 5). Using [11C]-nicotine and positron emission tomography (PET) imaging, cocaine-experienced monkeys showed significantly higher receptor availability in the hippocampus compared to cocaine-naive monkeys. A second goal was to examine the effects of nAChR agonists on multiple domains of cognitive performance in these same monkeys. For these studies, working memory was assessed using a delayed match-to-sample (DMS) task, associative learning and behavioral flexibility using stimulus discrimination and reversal learning tasks. When administered acutely, the nonselective high-efficacy agonist nicotine, the low-efficacy α4α2* subtype-selective agonist varenicline and the high-efficacy α7 subtype-selective agonist, PNU-282987 significantly improved DMS performance in both cocaine-naive and cocaine-experienced monkeys. Individual doses of nicotine and varenicline that engendered maximum cognitive enhancing effects on working memory did not affect discrimination or reversal learning, while PNU-282987 disrupted reversal learning in the cocaine-naive monkeys. These findings indicate that a cocaine self-administration history influenced nAChR distribution and the effects of nAChR agonists on cognitive performance, including a reduced sensitivity to the disrupting effects on reversal learning. The cognitive enhancing effects of nAChR agonists may be beneficial in combination with behavioral treatments for cocaine addiction.
机译:可卡因的使用与认知功能受损有关,这可能会对治疗结果产生负面影响。一种改善认知的药理策略涉及烟碱乙酰胆碱受体(nAChR)刺激。但是,慢性可卡因暴露对nAChR分布和功能的影响尚未被表征。因此,这项研究的一个目标是与具有年龄可比性的可卡因天真对照猴子相比,研究具有广泛可卡因自我管理史(n = 4;〜6年,平均摄入量,1463 mg / kg)的恒河猴中的nAChR可用性(n = 5)。使用[ 11 C]-烟碱和正电子发射断层扫描(PET)成像,与可卡因未使用过的猴子相比,可卡因经历过的猴子在海马中显示出明显更高的受体利用率。第二个目标是研究nAChR激动剂对这些相同猴子的多个认知表现域的影响。对于这些研究,工作记忆是使用延迟的样本匹配(DMS)任务,联想学习和行为灵活性(通过刺激识别和逆向学习任务)进行评估的。急性给药时,非选择性高效激动剂尼古丁,低效率α4α2*亚型选择性激动剂伐尼克兰和高效α7亚型选择性激动剂PNU-282987可显着提高可卡因初用和可卡因使用经验中的DMS性能。猴子。对工作记忆产生最大认知增强作用的尼古丁和伐尼克兰的单独剂量不影响歧视或逆向学习,而PNU-282987破坏了可卡因天真猴子的逆向学习。这些发现表明可卡因的自我管理史影响了nAChR的分布以及nAChR激动剂对认知能力的影响,包括对破坏性影响逆向学习的敏感性降低。与可卡因成瘾的行为治疗相结合,nAChR激动剂的认知增强作用可能是有益的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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