Institute of Physiology and Pathophysiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 17, Erlangen, 91056, Germany.
Institute of Anatomy I, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Eur J Neurosci. 2018 Feb;47(3):201-210. doi: 10.1111/ejn.13799. Epub 2018 Jan 11.
Spices in food and beverages and compounds in tobacco smoke interact with sensory irritant receptors of the transient receptor potential (TRP) cation channel family. TRPV1 (vanilloid type 1), TRPA1 (ankyrin 1) and TRPM8 (melastatin 8) not only elicit action potential signaling through trigeminal nerves, eventually evoking pungent or cooling sensations, but by their calcium conductance they also stimulate the release of calcitonin gene-related peptide (CGRP). This is measured as an index of neuronal activation to elucidate the chemo- and thermosensory transduction in the isolated mouse buccal mucosa of wild types and pertinent knockouts. We found that the lipophilic capsaicin, mustard oil and menthol effectively get access to the nerve endings below the multilayered squamous epithelium, while cigarette smoke and its gaseous phase were weakly effective releasing CGRP. The hydrophilic nicotine was ineffective unless applied unprotonated in alkaline (pH9) solution, activating TRPA1 and TRPV1. Also, mustard oil activated both these irritant receptors in millimolar but only TRPA1 in micromolar concentrations; in combination (1 mm) with heat (45 °C), it showed supraadditive, that is heat sensitizing, effects in TRPV1 and TRPA1 knockouts, suggesting action on an unknown heat-activated channel and mustard oil receptor. Menthol caused little CGRP release by itself, but in subliminal concentration (2 mm), it enabled a robust cold response that was absent in TRPM8 but retained in TRPA1 and strongly reduced by TRPM8 inhibitors. In conclusion, all three relevant irritant receptors are functionally expressed in the oral mucosa and play their specific roles in inducing neurogenic inflammation and sensitization to heat and cold.
食物和饮料中的香料以及烟草烟雾中的化合物与瞬时受体电位(TRP)阳离子通道家族的感觉刺激性受体相互作用。TRPV1(香草素 1 型)、TRPA1(锚蛋白 1)和 TRPM8(黑色素 8)不仅通过三叉神经引发动作电位信号,最终引起辛辣或冷却感,而且通过钙电导刺激降钙素基因相关肽(CGRP)的释放。这被测量为神经元激活的指标,以阐明野生型和相关基因敲除小鼠口腔颊黏膜中的化学和热敏感觉转导。我们发现亲脂性辣椒素、芥末油和薄荷醇有效地到达多层鳞状上皮下的神经末梢,而香烟烟雾及其气相则释放 CGRP 的效果较弱。亲水性尼古丁除非在碱性(pH9)溶液中未质子化,否则无效,从而激活 TRPA1 和 TRPV1。此外,芥末油以毫摩尔浓度有效激活这两种刺激性受体,但仅以微摩尔浓度有效激活 TRPV1;与热(45°C)联合(1 mM)时,它在 TRPV1 和 TRPA1 基因敲除小鼠中表现出超相加的、即热敏感的作用,表明作用于未知的热激活通道和芥末油受体。薄荷醇本身很少引起 CGRP 释放,但在亚阈浓度(2 mM)下,它能够引起强烈的冷反应,而在 TRPM8 中不存在这种反应,但在 TRPA1 中保留,并且在 TRPM8 抑制剂的作用下强烈减少。总之,口腔黏膜中功能性表达了这三种相关的刺激性受体,它们在诱导神经源性炎症以及对热和冷的敏感性方面发挥着各自的作用。