Department of Neuroscience, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Department of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Addict Biol. 2018 Jan;23(1):80-89. doi: 10.1111/adb.12475. Epub 2016 Nov 11.
A major challenge for treating cocaine addiction is the propensity for abstinent users to relapse. Two important triggers for relapse are cues associated with prior drug use and stressful life events. To study their interaction in promoting relapse during abstinence, we used the incubation model of craving and relapse in which cue-induced drug seeking progressively intensifies ('incubates') during withdrawal from extended-access cocaine self-administration. We tested rats for cue-induced cocaine seeking on withdrawal day (WD) 1. Rats were then subjected to repeated restraint stress or control conditions (seven sessions held between WD6 and WD14). All rats were tested again for cue-induced cocaine seeking on WD15, 1 day after the last stress or control session. Although controls showed a time-dependent increase in cue-induced cocaine seeking (incubation), rats exposed to repeated stress in early withdrawal exhibited a more robust increase in seeking behavior between WD1 and WD15. In separate stressed and control rats, equivalent cocaine seeking was observed on WD48. These results indicate that repeated stress in early withdrawal accelerates incubation of cocaine craving, although craving plateaus at the same level were observed in controls. However, 1 month after the WD48 test, rats subjected to repeated stress in early withdrawal showed enhanced cue-induced cocaine seeking following acute (24 hours) food deprivation stress. Together, these data indicate that chronic stress exposure enhances the initial rate of incubation of craving during early withdrawal, resulting in increased vulnerability to cue-induced relapse during this period, and may lead to a persistent increase in vulnerability to the relapse-promoting effects of stress.
治疗可卡因成瘾的一个主要挑战是禁欲使用者复发的倾向。复发的两个重要诱因是与先前药物使用相关的线索和压力生活事件。为了研究它们在禁欲期间促进复发的相互作用,我们使用了渴望和复发的孵化模型,其中线索引起的药物寻求在延长可卡因自我给药戒断期间逐渐加剧(“孵化”)。我们在戒断日(WD)1 对大鼠进行了线索诱导的可卡因寻求测试。然后,大鼠接受了重复的束缚应激或对照条件(在 WD6 和 WD14 之间进行了七次)。所有大鼠在 WD15 再次接受了线索诱导的可卡因寻求测试,即在最后一次应激或对照后 1 天。尽管对照组显示出与时间相关的线索诱导可卡因寻求增加(孵化),但在早期戒断期间暴露于重复应激的大鼠在 WD1 和 WD15 之间表现出更强的寻求行为增加。在单独的应激和对照大鼠中,在 WD48 观察到了相当的可卡因寻求。这些结果表明,早期戒断期间的重复应激加速了可卡因渴望的孵化,尽管对照组观察到渴望达到相同水平。然而,在 WD48 测试后 1 个月,在早期戒断期间暴露于重复应激的大鼠在急性(24 小时)食物剥夺应激后表现出增强的线索诱导可卡因寻求。总之,这些数据表明,慢性应激暴露会增加早期戒断期间渴望孵化的初始速度,导致在此期间对线索诱导的复发更加脆弱,并且可能导致对应激促进复发作用的持久脆弱性增加。