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TRPV2 激活通过产生一氧化氮参与调节小鼠的肠道运动。

Involvement of TRPV2 activation in intestinal movement through nitric oxide production in mice.

机构信息

Division of Cell Signaling, Okazaki Institute for Integrative Bioscience (National Institute for Physiological Sciences), National Institutes of Natural Sciences, Okazaki 444-8787, Japan.

出版信息

J Neurosci. 2010 Dec 8;30(49):16536-44. doi: 10.1523/JNEUROSCI.4426-10.2010.

Abstract

Transient receptor potential channel vanilloid 2 (TRPV2) can detect various stimuli such as temperature (>52 °C), stretch, and chemicals, including 2-aminoethoxydiphenyl borate, probenecid, and lysophospholipids. Although expressed in many tissues, including sensory and motor neurons, TRPV2 expression and function in the gastrointestinal tract is poorly understood. Here, we show TRPV2 expression in the murine intestine and its involvement in intestinal function. Almost all mouse intestinal intrinsic sensory and inhibitory motor neurons, both cell bodies and nerve fibers, showed TRPV2 immunoreactivity. Several known TRPV2 activators increased cytosolic Ca²+ concentrations and evoked TRPV2-like current responses in dissociated myenteric neurons. Interestingly, mechanical stimuli activated inward currents in a strength-dependent manner, which were inhibited by a TRPV2 inhibitor tranilast. TRPV2 activation in isolated intestine inhibited spontaneous circular muscle contraction, which did not occur in the presence of the TRPV2 antagonist, tetrodotoxin or nitro oxide (NO) synthase pathway inhibitors. Also, increased intestinal NO production was observed in response to a TRPV2 agonist, and gastrointestinal transit in vivo was accelerated by TRPV2 agonists or an NO donor. In conclusion, TRPV2 may contribute to intestinal motility through NO production, and TRPV2 is a promising target for controlling intestinal movement.

摘要

瞬时受体电位通道香草素 2(TRPV2)可以检测多种刺激,如温度(>52°C)、拉伸和化学物质,包括 2-氨基乙氧基二苯硼酸盐、丙磺舒和溶血磷脂。尽管在包括感觉和运动神经元在内的许多组织中表达,但 TRPV2 在胃肠道中的表达和功能知之甚少。在这里,我们展示了 TRPV2 在小鼠肠道中的表达及其在肠道功能中的作用。几乎所有的小鼠肠道内在感觉和抑制性运动神经元,包括细胞体和神经纤维,都显示出 TRPV2 免疫反应性。几种已知的 TRPV2 激活剂增加了细胞质 Ca²+浓度,并在分离的肌间神经元中诱发 TRPV2 样电流反应。有趣的是,机械刺激以强度依赖的方式激活内向电流,而 TRPV2 抑制剂曲尼司特可抑制这种电流。TRPV2 的激活抑制了离体肠的自发性环形肌收缩,而在存在 TRPV2 拮抗剂、河豚毒素或一氧化氮(NO)合酶途径抑制剂的情况下则不会发生这种情况。此外,TRPV2 激动剂可引起肠道 NO 产生增加,体内胃肠道转运加快。综上所述,TRPV2 可能通过 NO 产生来促进肠道运动,TRPV2 是控制肠道运动的有前途的靶点。

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