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羟基-α-山嵛醇激活感觉神经元中的TRPV1和TRPA1。

Hydroxy-alpha-sanshool activates TRPV1 and TRPA1 in sensory neurons.

作者信息

Koo Jae Yeon, Jang Yongwoo, Cho Hawon, Lee Chang-Hun, Jang Kyoung Hwa, Chang Yong Ha, Shin Jongheon, Oh Uhtaek

机构信息

The Sensory Research Center, Creative Research Initiatives, Seoul National University, College of Pharmacy, Gwanak, Shinlim-9 Dong Seoul, 151-742, Korea.

出版信息

Eur J Neurosci. 2007 Sep;26(5):1139-47. doi: 10.1111/j.1460-9568.2007.05743.x.

Abstract

Sanshools are major active ingredients of Zanthoxylum piperitum and are used as food additives in East Asia. Sanshools cause irritant, tingling and sometimes paresthetic sensations on the tongue. However, the molecular mechanism underlying the pungent or tingling sensation induced by sanshools is not known. Because many transient receptor potential (TRP) channels are responsible for the sensations induced by various spices and food additives, we expressed 17 TRP channels in human embryonic kidney (HEK) cells and investigated their activation by hydroxy-alpha-sanshool (HalphaSS) or hydroxy-beta-sanshool (HbetaSS) isolated from Zanthoxylum piperitum. It was found that HalphaSS, but not HbetaSS, depolarized sensory neurons with concomitant firing of action potentials and evoked inward currents. Among 17 TRP channels expressed in HEK cells, HalphaSS caused Ca(2+) influx in cells transfected with TRPV1 or TRPA1, and evoked robust inward currents in cells transfected with TRPV1 or TRPA1. In primary cultured sensory neurons, HalphaSS induced inward currents and Ca(2+) influx in a capsazepine-dependent manner. Moreover, HalphaSS-induced currents and Ca(2+) influx were greatly diminished in TRPV1(-/-) mice. HalphaSS evoked licking behavior when injected into a single hind paw of wild-type mice, but this was much reduced in TRPV1-deficient mice. These results indicate that TRPV1 and TRPA1 are molecular targets of HalphaSS in sensory neurons. We conclude that the activations of TRPV1 and TRPA1 by HalphaSS explain its unique pungent, tingling sensation.

摘要

山椒素是花椒的主要活性成分,在东亚地区用作食品添加剂。山椒素会在舌头上引起刺激、刺痛,有时还会有麻木感。然而,山椒素引起辛辣或刺痛感的分子机制尚不清楚。由于许多瞬时受体电位(TRP)通道负责各种香料和食品添加剂引起的感觉,我们在人胚肾(HEK)细胞中表达了17种TRP通道,并研究了从花椒中分离出的羟基-α-山椒素(HalphaSS)或羟基-β-山椒素(HbetaSS)对它们的激活作用。结果发现,HalphaSS而非HbetaSS使感觉神经元去极化,同时伴有动作电位发放并诱发内向电流。在HEK细胞中表达的17种TRP通道中,HalphaSS导致转染了TRPV1或TRPA1的细胞内Ca(2+)内流,并在转染了TRPV1或TRPA1的细胞中诱发强烈的内向电流。在原代培养的感觉神经元中,HalphaSS以辣椒素受体拮抗剂(capsazepine)依赖的方式诱导内向电流和Ca(2+)内流。此外,在TRPV1(-/-)小鼠中,HalphaSS诱导的电流和Ca(2+)内流大大减少。将HalphaSS注射到野生型小鼠的单个后爪时会诱发舔舐行为,但在TRPV1缺陷小鼠中这种行为大大减少。这些结果表明,TRPV1和TRPA1是感觉神经元中HalphaSS的分子靶点。我们得出结论,HalphaSS对TRPV1和TRPA1所产生的激活作用解释了其独特的辛辣、刺痛感。

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