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
Abstract
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.