首页> 美国卫生研究院文献>Acta Pharmacologica Sinica >A pivotal role for the activation of TRPV3 channel in itch sensations induced by the natural skin sensitizer carvacrol
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A pivotal role for the activation of TRPV3 channel in itch sensations induced by the natural skin sensitizer carvacrol

机译:TRPV3通道在由天然皮肤敏化剂香芹酚引起的瘙痒感中激活的关键作用

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摘要

Itching is an intricate, common symptom of dermatologic and systemic diseases, and both TRPV3 and TRPA1 channels have been suggested to function as downstream effector targets. But the relative contributions of TRPV3 and TRPA1 to itch sensation in vivo remain unclear. To dissect the role of TRPA1 or TRPV3 in the cutaneous sensation of itching, we took the advantage of a natural compound carvacrol from oregano, and examined its effect on the induction of scratching behavior in mice. We showed that the intradermal injection of carvacrol (0.01%, 0.1% and 1%, 50 μL) induced scratching in a concentration-dependent manner. But in TRPV3-knockout mice, the scratching induced by carvacrol (1%, 50 μL) was markedly decreased by approximately 64% (from 275 scratching bouts down to 90) within 60 min. Further analysis revealed that TRPV3-knockout caused a reduction of scratching bouts for approximately 40% in the first 20 min (the initial phase), whereas the scratching bouts were reduced by approximately 90% in the last 40 min (the sustained phase). These results were in consistence with those in our whole-cell recordings in HEK-293T cells expressing either TRPA1 or TRPV3: carvacrol exhibited similar potencies in activating either TRPA1 or TRPV3, but carvacrol-activated TRPA1 current showed a rapid desensitization, which was reduced by approximately 90% within 5 min before a complete washout, whereas carvacrol-induced TRPV3 current showed a slow desensitization that caused less than 30% of current reduction in 10 min and left a significant residual TRPV3 current after washout. Our results demonstrate that carvacrol from plant oregano is a skin sensitizer or allergen; TRPV3 is involved in the initial phase and the sustained phase of pruritus, whereas TRPA1 likely contributes to the initial phase.
机译:瘙痒是皮肤病和全身性疾病的复杂,常见症状,并且TRPV3和TRPA1通道均被建议充当下游效应物靶标。但是,TRPV3和TRPA1对体内痒感的相对贡献尚不清楚。为了剖析TRPA1或TRPV3在皮肤瘙痒感中的作用,我们利用牛至的天然化合物香芹酚的优势,并研究了其对小鼠抓挠行为的诱导作用。我们发现皮内注射香芹酚(0.01%,0.1%和1%,50μL)以浓度依赖的方式引起抓挠。但是在TRPV3基因敲除小鼠中,香芹酚(1%,50μL)引起的刮擦在60分钟内显着减少了约64%(从275次刮擦回落到90次)。进一步的分析表明,TRPV3敲除导致前20分钟(初始阶段)的抓挠减少约40%,而最后40分钟(持续阶段)的抓挠减少约90%。这些结果与我们在表达TRPA1或TRPV3的HEK-293T细胞中的全细胞记录一致:香芹酚在激活TRPA1或TRPV3方面显示出相似的效力,但是香芹酚激活的TRPA1电流显示出快速的脱敏作用,其降低了在完全冲洗之前的5分钟内约90%,而香芹酚诱导的TRPV3电流表现出缓慢的脱敏作用,在10分钟内引起的电流减少量不到30%,并且在冲洗后留下了大量的残余TRPV3电流。我们的结果表明,植物牛至中的香芹酚是一种皮肤致敏剂或过敏原。 TRPV3参与瘙痒的初始阶段和持续阶段,而TRPA1可能参与了瘙痒的初始阶段。

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