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

被引:4
|
作者
Kim, Jin Cheol [1 ]
Kim, Han Bi [1 ]
Shim, Won-Sik [2 ]
Kwak, In Suk [3 ]
Chung, Bo Young [1 ]
Kang, Seok Young [1 ]
Park, Chun Wook [1 ]
Kim, Hye One [1 ]
机构
[1] Hallym Univ, Kangnam Sacred Heart Hosp, Coll Med, Dept Dermatol, Seoul 07441, South Korea
[2] Gachon Univ, Coll Pharm, Incheon, South Korea
[3] Hallym Univ, Hangang Sacred Heart Hosp, Coll Med, Dept Anesthesiol & Pain Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
itch; pruritus; carvacrol; transient receptor potential vanilloid-3; thymic stromal lymphopoietin; oregano; TRPV3; CHANNEL; BURN SCARS; MUTATION; ITCH;
D O I
10.2340/00015555-3855
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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, beta-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.
引用
收藏
页数:7
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