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Transient receptor potential melastatin-3 (TRPM3) mediates nociceptive-like responses in Hydra vulgaris

机译:瞬态受体电位melastatin-3(TRPM3)介导寻常的九头蛇伤害性样反应

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摘要

The ability of mammals to feel noxious stimuli lies in a heterogeneous group of primary somatosensory neurons termed nociceptors, which express specific membrane receptors, such as the Transient Receptor Potential (TRP) family. Here, we show that one of the most important nociceptive-like pathways is conserved in the freshwater coelenterate Hydra vulgaris, the most primitive organism possessing a nervous system. In particular, we found that H. vulgaris expresses TRPM3, a nociceptor calcium channel involved in the detection of noxious heat in mammals. Furthermore, we detected that both heat shock and TRPM3 specific agonist (i.e., pregnenolone sulfate) induce the modulation of the heat shock protein 70 (HSP70) and the nitric oxide synthase (NOS), two genes activated by TRP-mediated heat painful stimuli in mammals. As expected, these effects are inhibited by a TRPM3 antagonist (i.e., mefenamicacid). Interestingly, the TRPM3 agonist and heat shock also induce the expression of nuclear transcription erythroid 2-related factor (Nrf2) and superoxide dismutase (SOD), known markers of oxidative stress; noteworthy gene expression was also inhibited by the TRPM3 antagonist. As a whole, our results demonstrate the presence of conserved molecular oxidative/nociceptive-like pathways at the primordial level of the animal kingdom.
机译:哺乳动物感觉到有害刺激的能力在于称为感觉感受器的异质性初级体感神经元组,其表达特定的膜受体,例如瞬时受体电位(TRP)家族。在这里,我们表明最重要的类似伤害感受的途径之一是在淡水腔肠寻常水蛇(Hydra vulgaris)(一种具有神经系统的最原始生物)中得以保留。特别地,我们发现寻常型嗜血​​杆菌表达TRPM3,这是一种伤害性钙离子通道,参与哺乳动物中有害热的检测。此外,我们检测到热休克和TRPM3特异性激动剂(即孕烯醇酮硫酸盐)均诱导热休克蛋白70(HSP70)和一氧化氮合酶(NOS)的调节,这两个基因是由TRP介导的热痛刺激激活的。哺乳动物。如所预期的,这些作用被TRPM3拮抗剂(即甲芬那酸)抑制。有趣的是,TRPM3激动剂和热休克还诱导了核转录红系2相关因子(Nrf2)和超氧化物歧化酶(SOD)的表达,这是氧化应激的已知标志物。值得注意的是,TRPM3拮抗剂也抑制了基因表达。总体而言,我们的结果表明在动物界的原始水平上存在保守的分子氧化/伤害感受样途径。

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