Dakwar E, Hart C L, Levin F R, Nunes E V, Foltin R W
New York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
Department of Psychology, Columbia University, New York, NY, USA.
Mol Psychiatry. 2017 Jan;22(1):76-81. doi: 10.1038/mp.2016.39. Epub 2016 Apr 19.
Repeated drug consumption may progress to problematic use by triggering neuroplastic adaptations that attenuate sensitivity to natural rewards while increasing reactivity to craving and drug cues. Converging evidence suggests a single sub-anesthetic dose of the N-methyl-D-aspartate receptor antagonist ketamine may work to correct these neuroadaptations and restore motivation for non-drug rewards. Using an established laboratory model aimed at evaluating behavioral shifts in the salience of cocaine now vs money later, we found that ketamine, as compared to the control, significantly decreased cocaine self-administration by 67% relative to baseline at greater than 24 h post-infusion, the most robust reduction observed to date in human cocaine users and the first to involve mechanisms other than stimulant or dopamine agonist effects. These findings signal new directions in medication development for substance use disorders.
反复使用药物可能会引发神经可塑性适应,从而导致问题性使用,这种适应会减弱对自然奖励的敏感性,同时增加对渴望和药物线索的反应性。越来越多的证据表明,单次亚麻醉剂量的N-甲基-D-天冬氨酸受体拮抗剂氯胺酮可能有助于纠正这些神经适应,并恢复对非药物奖励的动机。使用一个既定的实验室模型来评估当前可卡因与日后金钱的显著性行为转变,我们发现,与对照组相比,氯胺酮在输注后超过24小时时,相对于基线显著降低了67%的可卡因自我给药量,这是迄今为止在人类可卡因使用者中观察到的最显著的减少,也是首次涉及兴奋剂或多巴胺激动剂作用以外机制的减少。这些发现为物质使用障碍的药物开发指明了新方向。