Department of Psychiatry, University of California, San Diego, La Jolla, United States.
Department of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, United States.
Elife. 2024 Nov 1;12:RP90422. doi: 10.7554/eLife.90422.
Addiction is commonly characterized by escalation of drug intake, compulsive drug seeking, and continued use despite harmful consequences. However, the factors contributing to the transition from moderate drug use to these problematic patterns remain unclear, particularly regarding the role of sex. Many preclinical studies have been limited by small sample sizes, low genetic diversity, and restricted drug access, making it challenging to model significant levels of intoxication or dependence and translate findings to humans. To address these limitations, we characterized addiction-like behaviors in a large sample of >500 outbred heterogeneous stock (HS) rats using an extended cocaine self-administration paradigm (6 hr/daily). We analyzed individual differences in escalation of intake, progressive ratio (PR) responding, continued use despite adverse consequences (contingent foot shocks), and irritability-like behavior during withdrawal. Principal component analysis showed that escalation of intake, progressive ratio responding, and continued use despite adverse consequences loaded onto a single factor that was distinct from irritability-like behaviors. Categorizing rats into resilient, mild, moderate, and severe addiction-like phenotypes showed that females exhibited higher addiction-like behaviors, with a lower proportion of resilient individuals compared to males. These findings suggest that, in genetically diverse rats with extended drug access, escalation of intake, continued use despite adverse consequences, and PR responding are highly correlated measures of a shared underlying construct. Furthermore, our results highlight sex differences in resilience to addiction-like behaviors.
成瘾通常表现为药物摄入的增加、强迫性觅药以及尽管有不良后果仍继续使用。然而,导致从适度药物使用转变为这些问题模式的因素仍不清楚,特别是关于性别的作用。许多临床前研究受到样本量小、遗传多样性低以及药物获取受限的限制,使得难以模拟显著的中毒或依赖水平,并将研究结果转化为人类。为了解决这些限制,我们使用扩展的可卡因自我给药范式(每天 6 小时)对超过 500 只异交杂合 stock (HS) 大鼠进行了大量研究,以描述类似于成瘾的行为。我们分析了摄入增加、递增比例(PR)反应、尽管有不良后果(伴随足电击)仍继续使用以及戒断期间类似烦躁的行为的个体差异。主成分分析表明,摄入增加、递增比例反应和尽管有不良后果仍继续使用加载到一个单独的因素上,与类似烦躁的行为不同。将大鼠分为具有弹性、轻度、中度和严重类似成瘾表型的大鼠表明,雌性表现出更高的类似成瘾行为,与雄性相比,具有弹性的个体比例较低。这些发现表明,在具有扩展药物获取的遗传多样性大鼠中,摄入增加、尽管有不良后果仍继续使用和 PR 反应是共享潜在结构的高度相关测量指标。此外,我们的结果强调了对类似成瘾行为的弹性的性别差异。