赛拉嗪是卡巴阿片受体的激动剂,对阿片拮抗剂的反应具有性别特异性

Madigan L. Bedard , Xi-Ping Huang , Jackson G. Murray , Alexandra C. Nowlan , Sara Y. Conley , Sarah E. Mott , Samuel J. Loyack , Calista A. Cline , Caroline G. Clodfelter , Nabarun Dasgupta , Brian Krumm , Bryan L. Roth , Zoe A. McElligott
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引用次数: 0

摘要

在不受管制的毒品供应中,异丙嗪的使用率越来越高,通常与芬太尼混合使用,因此有必要了解其药理学。尽管政界人士和公共卫生官员对其进行了评论,但人们仍不清楚恶嗪对纳洛酮疗效的影响,也很少有研究单独对其进行研究。在这里,我们研究了单独使用和与芬太尼联用对小鼠几种行为的影响。令人惊奇的是,纳洛酮会促使小鼠在服用异丙嗪和芬太尼/异丙嗪联合给药后戒断,而且雌性小鼠对纳洛酮的敏感性更高。此外,异丙嗪是卡巴阿片受体的完全激动剂,这也是纳洛酮敏感性的潜在机制。最后,我们证明了甲氧苄啶对卡巴阿片拮抗剂的惊人效果,这与公共卫生方面的考虑有关。这些数据解决了一个正在发生的健康危机,并将有助于为重要的政策和医疗保健决策提供信息。一句话总结我们提出了关于恶嗪和芬太尼药理学的令人惊讶的新见解,对临床实践和一线公共卫生具有直接影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Xylazine is an agonist at kappa opioid receptors and exhibits sex-specific responses to opioid antagonism

Xylazine is in the unregulated drug supply at increasing rates, usually combined with fentanyl, necessitating understanding of its pharmacology. Despite commentary from politicians, and public health officials, it is unknown how xylazine impacts naloxone efficacy, and. few studies have examined it alone. Here, we examine the impact of xylazine alone and in combination with fentanyl on several behaviors in mice. Surprisingly, naloxone precipitates withdrawal from xylazine and fentanyl/xylazine coadministration, with enhanced sensitivity in females. Further, xylazine is a full agonist at kappa opioid receptors, a potential mechanism for its naloxone sensitivity. Finally, we demonstrate surprising effects of xylazine to kappa opioid antagonism, which are relevant for public health considerations. These data address an ongoing health crisis and will help inform critical policy and healthcare decisions.

One-sentence summary

We present surprising new insights into xylazine and fentanyl pharmacology with immediate implications for clinical practice and frontline public health.

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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
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118 days
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