Zebrafish model reveals xylazine impairs tissue homeostasis and cell interactions, indicating treatment implications for skin wounds.
The veterinary sedative and alpha-2 adrenergic receptor (α2AR) agonist xylazine, found in the illicit opioid supply, is associated with cutaneous wounds in humans. Here, we develop a larval zebrafish model of xylazine-induced tissue damage to investigate the mechanisms by which xylazine affects the skin. Xylazine treatment causes keratinocyte extrusion, tissue-wide skin contraction, and the disruption of basal keratinocyte cell-cell interactions in zebrafish larvae. Notably, other α2AR agonists cannot recapitulate most of these effects. Xylazine was recently described as a kappa opioid receptor (κOR) agonist, and we find that both xylazine and a separate κOR agonist can act directly on epithelial cells to drive cellular contraction and disrupt tissue homeostasis. Our model suggests that xylazine may disrupt skin homeostasis through a direct mechanism involving epithelial cells and κOR, which may be of importance for the treatment of these wounds.
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Robertson et al. (2026) studied this question.
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