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TRPM8 在内脏传入功能中的新作用。

A novel role for TRPM8 in visceral afferent function.

机构信息

Nerve-Gut Research Laboratory, Department of Gastroenterology & Hepatology, Hanson Institute, Royal Adelaide Hospital, Adelaide, South Australia, Australia Discipline of Medicine, University of Adelaide, Adelaide, South Australia, Australia Discipline of Physiology, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

Pain. 2011 Jul;152(7):1459-1468. doi: 10.1016/j.pain.2011.01.027. Epub 2011 Apr 13.

Abstract

Transient receptor potential ion channel melastatin subtype 8 (TRPM8) is activated by cold temperatures and cooling agents, such as menthol and icilin. Compounds containing peppermint are reported to reduce symptoms of bowel hypersensitivity; however, the underlying mechanisms of action are unclear. Here we determined the role of TRPM8 in colonic sensory pathways. Laser capture microdissection, quantitative reverse transcription-polymerase chain reaction (RT-PCR), immunofluorescence, and retrograde tracing were used to localise TRPM8 to colonic primary afferent neurons. In vitro extracellular single-fibre afferent recordings were used to determine the effect of TRPM8 channel activation on the chemosensory and mechanosensory function of colonic high-threshold afferent fibres. TRPM8 mRNA was present in colonic DRG neurons, whereas TRPM8 protein was present on nerve fibres throughout the wall of the colon. A subpopulation (24%, n=58) of splanchnic serosal and mesenteric afferents tested responded directly to icilin (5 μmol/L). Subsequently, icilin significantly desensitised afferents to mechanical stimulation (P<.0001; n=37). Of the splanchnic afferents responding to icilin, 21 (33%) also responded directly to the TRPV1 agonist capsaicin (3 μmol/L), and icilin reduced the direct chemosensory response to capsaicin. Icilin also prevented mechanosensory desensitization and sensitization induced by capsaicin and the TRPA1 agonist AITC (40 μmol/L), respectively. TRPM8 is present on a select population of colonic high threshold sensory neurons, which may also co-express TRPV1. TRPM8 couples to TRPV1 and TRPA1 to inhibit their downstream chemosensory and mechanosensory actions.

摘要

瞬时受体电位阳离子通道 melastatin 亚家族 8(TRPM8)受低温和冷却剂(如薄荷醇和异硫氰酸 icilin)激活。含有薄荷的化合物据报道可减轻肠道高敏症状;然而,其作用机制尚不清楚。在这里,我们确定了 TRPM8 在结肠感觉通路中的作用。激光捕获显微切割、定量逆转录聚合酶链反应(RT-PCR)、免疫荧光和逆行追踪用于将 TRPM8 定位到结肠初级传入神经元。体外细胞外单纤维传入记录用于确定 TRPM8 通道激活对结肠高阈值传入纤维的化学感觉和机械感觉功能的影响。TRPM8 mRNA 存在于结肠 DRG 神经元中,而 TRPM8 蛋白存在于结肠壁的神经纤维上。测试的肠系膜内脏传入神经中的一个亚群(24%,n=58)直接对 icilin(5 μmol/L)有反应。随后,icilin 显著使传入纤维对机械刺激脱敏(P<.0001;n=37)。对 icilin 有反应的肠系膜传入神经中,有 21 个(33%)也直接对 TRPV1 激动剂辣椒素(3 μmol/L)有反应,icilin 降低了对辣椒素的直接化学感觉反应。icilin 还分别防止了辣椒素和 TRPA1 激动剂 AITC(40 μmol/L)引起的机械感觉脱敏和敏化。TRPM8 存在于结肠高阈值感觉神经元的一个选择群体上,这些神经元也可能共同表达 TRPV1。TRPM8 与 TRPV1 和 TRPA1 偶联,以抑制它们的下游化学感觉和机械感觉作用。

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