Suppr超能文献

瞬时受体电位香草酸亚型 3 通道在角质形成细胞中的激活可诱发人类瘙痒。

Activation of Transient Receptor Potential Vanilloid-3 Channels in Keratinocytes Induces Pruritus in Humans.

机构信息

Department of Dermatology, Kangnam Sacred Heart Hospital, Hallym University, 07441 Seoul, Korea.

出版信息

Acta Derm Venereol. 2021 Aug 18;101(8):adv00517. doi: 10.2340/00015555-3855.

Abstract

Carvacrol, a natural transient receptor potential vanilloid-3 activator, has been reported to cause pruritus in mice. This study aimed to evaluate the effects of carvacrol and various antipruritic agents in humans. A stimulation test with carvacrol, β-alanine, and histamine was performed. After application of the pruritic solutions, the skin was stimulated with pinpricks. In inhibition test A, Forsythia suspensa extract, containing forsythoside B (a transient receptor potential vanilloid-3 inhibitor), was applied by pricking prior to stimulation with pruritogens. In inhibition test B, olopatadine solution, tacrolimus ointment, and Scutellaria baicalensis root extract were applied, and carvacrol was applied to the same region. Carvacrol induces moderate pruritus in humans. The pruritus was relieved by Forsythia suspensa extract and olopatadine solution after 20 min of application and by tacrolimus ointment and Scutellaria baicalenis extract after 24 h of application. These results suggest that carvacrol is a pruritogen in humans, and that carvacrol-induced pruritus is inhibited by various antipruritic agents.

摘要

香芹酚,一种天然瞬时受体电位香草醛 3 激活剂,已被报道在小鼠中引起瘙痒。本研究旨在评估香芹酚和各种止痒剂在人类中的作用。进行了香芹酚、β-丙氨酸和组氨酸的刺激试验。在应用瘙痒溶液后,用针刺刺激皮肤。在抑制试验 A 中,应用连翘提取物(含连翘酯苷 B,瞬时受体电位香草醛 3 抑制剂)进行针刺,然后用致痒原刺激。在抑制试验 B 中,应用奥洛他定溶液、他克莫司软膏和黄芩根提取物,并将香芹酚应用于同一区域。香芹酚在人类中引起中度瘙痒。应用 20 分钟后,连翘提取物和奥洛他定溶液可缓解瘙痒,应用 24 小时后,他克莫司软膏和黄芩根提取物也可缓解瘙痒。这些结果表明香芹酚是人类的致痒原,各种止痒剂可抑制香芹酚诱导的瘙痒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ca/9425626/579a3ce26d55/ActaDV-101-8-96-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验