Kimble Violet M, Nunes Eric J, Rajadhyaksha Anjali M, Addy Nii A
Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA; Interdepartmental Neuroscience Program, Yale University, New Haven, CT, USA.
Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Behav Brain Res. 2025 May 3;490:115613. doi: 10.1016/j.bbr.2025.115613.
Periods of cocaine abstinence are associated with a high risk of relapse, often triggered by exposure to drug-associated cues. Previous research has implicated L-type calcium channels (LTCCs) in drug-seeking behaviors, yet their role in cue-induced relapse, particularly in females, remains underexplored. This study investigated the effects of LTCC inhibition on cue-induced cocaine-seeking behavior during abstinence in female Sprague-Dawley rats. Following a 10-day cocaine self-administration and a 14-day forced abstinence period, the rats were tested for cue-induced cocaine-seeking after receiving systemic administration of isradipine, a non-selective LTCC inhibitor (0.0 mg/kg, 0.1 mg/kg, 0.4 mg/kg, or 1.2 mg/kg, i.p.). Isradipine significantly reduced cue-induced cocaine-seeking in a dose-dependent manner without affecting cocaine-taking or natural reward-taking or seeking behaviors. Notably, these findings in females were comparable to our prior results observed in males, demonstrating that LTCC inhibition selectively attenuates the impact of cocaine-associated cues across sexes. These results highlight the translational potential of LTCCs as a therapeutic agent to reduce relapse risk in cocaine-dependent individuals. This study underscores the importance of considering sex-specific mechanisms in addiction treatment and calls for further research into LTCCs as a target for relapse prevention.
可卡因戒断期与高复发风险相关,通常由接触与药物相关的线索引发。先前的研究表明L型钙通道(LTCCs)与觅药行为有关,但其在线索诱导的复发中的作用,尤其是在雌性动物中的作用,仍未得到充分研究。本研究调查了LTCC抑制对雌性Sprague-Dawley大鼠戒断期间线索诱导的可卡因觅求行为的影响。在进行10天的可卡因自我给药和14天的强制戒断期后,大鼠接受非选择性LTCC抑制剂伊拉地平(0.0mg/kg、0.1mg/kg、0.4mg/kg或1.2mg/kg,腹腔注射)全身给药,然后测试线索诱导的可卡因觅求行为。伊拉地平以剂量依赖性方式显著减少线索诱导的可卡因觅求行为,而不影响可卡因摄取或自然奖赏摄取及觅求行为。值得注意的是,这些在雌性动物中的发现与我们先前在雄性动物中观察到的结果相当,表明LTCC抑制可选择性减弱可卡因相关线索对不同性别的影响。这些结果突出了LTCCs作为一种治疗药物在降低可卡因依赖个体复发风险方面的转化潜力。本研究强调了在成瘾治疗中考虑性别特异性机制的重要性,并呼吁进一步研究将LTCCs作为预防复发的靶点。