Pickens Charles L, Aurand Lexia, Hunt Joshua, Fisher Hayley
Department of Psychological Sciences, Kansas State University, Manhattan, Kansas, USA.
Behav Pharmacol. 2017 Jun;28(4):294-302. doi: 10.1097/FBP.0000000000000289.
Previous exposure to a variety of drugs of abuse has been shown to cause long-term impairments in reversal learning and reinforcer devaluation tasks. However, there is mixed evidence in the literature for a long-term effect of ketamine exposure on reversal learning and the long-term effect of ketamine exposure on devaluation is not known. We determined whether repeated injections of an anesthetic dose of ketamine would lead to impairments in choice reversal learning after discrimination learning or impairments in reinforcer devaluation. In two experiments, rats received three injections once-daily of ketamine (100 mg/kg, intraperitoneally) or saline and then began behavioral training 19 days later so that the key reversal learning and devaluation tests would occur about 1 month after the final ketamine injection. This ketamine exposure regimen did not impair learning in our discrimination task, but led to an increase in perseverative errors in reversal learning. However, the same ketamine exposure regimen (or injections of a lower 50 mg/kg dose) had no effect on behavior in the devaluation task. The behavioral patterns observed suggest possible neural mechanisms for the effects of ketamine, but future neurobiological investigations will be needed to isolate these mechanisms.
先前接触多种滥用药物已被证明会在逆向学习和强化物贬值任务中导致长期损伤。然而,文献中关于氯胺酮暴露对逆向学习的长期影响存在混杂的证据,且氯胺酮暴露对贬值的长期影响尚不清楚。我们确定了重复注射麻醉剂量的氯胺酮是否会导致辨别学习后选择逆向学习受损或强化物贬值受损。在两项实验中,大鼠每天接受一次氯胺酮(100mg/kg,腹腔注射)或生理盐水的三次注射,然后在19天后开始行为训练,以便关键的逆向学习和贬值测试在最后一次氯胺酮注射后约1个月进行。这种氯胺酮暴露方案并未损害我们辨别任务中的学习,但导致逆向学习中持续性错误增加。然而,相同的氯胺酮暴露方案(或注射较低的50mg/kg剂量)对贬值任务中的行为没有影响。观察到的行为模式提示了氯胺酮作用的可能神经机制,但未来需要进行神经生物学研究来分离这些机制。