Acetone-Ether-Water Mouse Model of Persistent Itch Fully Resolves Without Latent Pruritic or Cross-Modality Priming.

IF 1.6 Q3 DERMATOLOGY
Zachary K Ford, Adam J Kirry, Steve Davidson
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Abstract

Hyperalgesic priming is a model of the transition from acute to chronic pain. Whether a similar mechanism exists for "pruritic priming" of itch is unknown. Here, we tested the hypothesis that itchy skin in a commonly used mouse model of dry skin pruritus develops latent sensitization after resolution. Acetone-ether-water (AEW) treatment induced a dry and itchy skin condition in the mouse cheek that elicited site-directed scratching behavior. After cessation of treatment and the complete resolution of AEW-induced scratching, histaminergic and non-histaminergic pruritogens were administered to the cheek to test for altered site-directed scratching and wiping behavior. Each pruritogen was also tested following the resolution of carrageenan-induced nociceptor hypersensitivity to test for cross-modality priming. Peak AEW-induced scratching occurred 24 h after the final day of treatment, and 5 days were required for scratching levels to return to baseline. Likewise, epidermal thickening was the greatest on the final treatment day and completely returned to baseline after 5 days. After the resolution of itchy cheek skin, acute histamine- and non-histamine-evoked scratching and wiping behaviors were unchanged, nor were scratching and wiping behaviors to acute pruritogens altered after the resolution of carrageenan-induced hypersensitivity. The results indicate that persistent itch due to dry skin likely resolves completely, without producing a latent primed response to subsequent pruritic stimuli. We conclude that the mechanisms regulating hyperalgesic priming are likely distinct from pruritic signaling in the dry and itchy skin model.

丙酮-醚-水小鼠持续瘙痒模型完全解决,无潜伏性瘙痒或跨模态启动。
痛觉过敏启动是急性疼痛向慢性疼痛过渡的一个模型。对于瘙痒的“瘙痒启动”是否存在类似的机制尚不清楚。在这里,我们测试了一种假设,即在一种常用的干性皮肤瘙痒小鼠模型中,皮肤瘙痒在消退后会产生潜在的致敏性。丙酮醚水(AEW)处理诱导小鼠脸颊皮肤干燥发痒,引发部位定向抓挠行为。在停止治疗和aew引起的抓挠完全消退后,组胺能和非组胺能搔痒剂被施用于脸颊,以测试部位定向抓挠和擦拭行为的改变。在角叉菜胶诱导的痛觉感受器超敏反应解决后,还对每种瘙痒剂进行了测试,以测试跨模态启动。aew诱导的抓痕峰值发生在治疗最后一天24小时后,抓痕水平需要5天才能恢复到基线水平。同样,表皮增厚在最后治疗日最大,5天后完全恢复到基线。在脸颊皮肤瘙痒消退后,急性组胺和非组胺诱发的抓挠和擦拭行为没有改变,卡拉胶诱导的超敏反应消退后,对急性瘙痒剂的抓挠和擦拭行为也没有改变。结果表明,由于皮肤干燥引起的持续瘙痒可能会完全解决,而不会对随后的瘙痒刺激产生潜在的启动反应。我们的结论是,在干燥和发痒的皮肤模型中,调节痛觉过敏启动的机制可能不同于瘙痒信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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