Department of Physiology & Pharmacology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157, United States of America.
Department of Biostatistics, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157, United States of America.
Pharmacol Biochem Behav. 2023 Apr;225:173545. doi: 10.1016/j.pbb.2023.173545. Epub 2023 Mar 31.
Cocaine use disorder (CUD) is a significant problem worldwide, with no FDA-approved treatments. Epidemiological data indicate that only about 17 % of people that use cocaine will meet DSM criteria for CUD. Thus, the identification of biomarkers predictive of eventual cocaine use may be of great value. Two potentially useful predictors of CUD are social hierarchies in nonhuman primates and delay discounting. Both social rank and preference for a smaller, immediate reinforcer relative to a larger, delayed reinforcer have been predictive of CUD. Therefore, we wanted to determine if there was also a relationship between these two predictors of CUD. In the present study, monkeys cocaine-naive responded under a concurrent schedule of 1- vs. 3-food pellets and delivery of the 3-pellet option was delayed. The primary dependent variable was the indifference point (IP), which is the delay that results in 50 % choice for both options. In the initial determination of IP, there were no differences based on sex or social rank of the monkeys. When the delays were redetermined after ~25 baseline sessions (range 5-128 sessions), dominant females and subordinate males showed the largest increases in IP scores from the first determination to the second. Because 13 of these monkeys had prior PET scans of the kappa opioid receptor (KOR), we examined the relationship between KOR availability and IP values and found that the change in IP scores from the first to the second determination significantly negatively predicted average KOR availability in most brain regions. Future studies will examine acquisition to cocaine self-administration in these same monkeys, to determine if IP values are predictive of vulnerability to cocaine reinforcement.
可卡因使用障碍(CUD)是一个全球性的重大问题,目前尚无获得 FDA 批准的治疗方法。流行病学数据表明,只有约 17%的可卡因使用者符合 CUD 的 DSM 标准。因此,识别最终可能导致可卡因使用的生物标志物可能具有重要价值。两种可能有用的 CUD 预测因子是非人类灵长类动物中的社会等级和延迟折扣。社会等级和对较小的即时强化物的偏好相对于较大的延迟强化物的偏好都可以预测 CUD。因此,我们想确定这两种 CUD 预测因子之间是否也存在关系。在本研究中,可卡因未使用的猴子在 1-与 3-食物颗粒的同时日程安排下做出反应,并且延迟了 3-颗粒选项的交付。主要的因变量是无差异点(IP),即导致两种选择各有 50%选择的延迟。在 IP 的初始确定中,猴子的性别或社会等级没有差异。当在大约 25 个基线课程(范围 5-128 个课程)后重新确定延迟时,支配型雌性和从属型雄性的 IP 评分从第一次确定到第二次确定时的增加幅度最大。因为这些猴子中有 13 只先前进行过κ阿片受体(KOR)的 PET 扫描,我们检查了 KOR 可用性与 IP 值之间的关系,并发现从第一次到第二次确定时的 IP 评分变化显著负预测了大多数脑区的平均 KOR 可用性。未来的研究将在这些相同的猴子中检查可卡因自我给药的获取情况,以确定 IP 值是否可预测对可卡因强化的易感性。