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The roles of iPLA2 TRPM8 and TRPA1 in chemically induced cold hypersensitivity

机译:iPLA2TRPM8和TRPA1在化学性感冒超敏反应中的作用

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摘要

BackgroundThe cooling agents menthol and icilin act as agonists at TRPM8 and TRPA1. In vitro, activation of TRPM8 by icilin and cold, but not menthol, is dependent on the activity of a sub-type of phospholipase A2, iPLA2. Lysophospholipids (e.g. LPC) produced by PLA2 activity can also activate TRPM8. The role of TRPA1 as a primary cold sensor in vitro is controversial, although there is evidence that TRPA1 plays a role in behavioural responses to noxious cold stimuli. In this study, we have investigated the roles of TRPM8 and TRPA1 and the influence of iPLA2 on noxious cold sensitivities in naïve animals and after local administration of menthol, icilin and LPC. The roles of the channels in cold sensitivity were investigated in mice lacking either TRPM8 (Trpm8-/-) or TRPA1 (Trpa1-/-).
机译:背景凉爽剂薄荷醇和icilin在TRPM8和TRPA1中充当激动剂。在体外,依西林和冷而不是薄荷醇对TRPM8的激活取决于磷脂酶A2亚型iPLA2的活性。 PLA2活性产生的溶血磷脂(例如LPC)也可以激活TRPM8。尽管有证据表明TRPA1在对有害冷刺激的行为反应中起作用,但它在体外作为主要的冷传感器的作用仍存在争议。在这项研究中,我们调查了薄荷,局部服用薄荷醇,艾西林和LPC后,TRPM8和TRPA1的作用以及iPLA2对纯净动物有害冷感的影响。在缺少TRPM8(Trpm8 -/-)或TRPA1(Trpa1 -/-)的小鼠中研究了通道在冷敏感性中的作用。

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