Mechanical and cold polymodality coexist in tactile peripheral afferents, and it's not mediated by TRPM8.

IF 2.8 3区 医学 Q2 NEUROSCIENCES
M Danilo Boada, Silvia Gutierrez
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引用次数: 0

Abstract

In the mammalian somatosensory system, polymodality is defined as the competence of some neurons to respond to multiple forms of energy (e.g., mechanical and thermal). This ability is thought to be an exclusive property of nociceptive neurons (polymodal C-fiber nociceptors) and one of the pillars of nociceptive peripheral plasticity. The current study uncovered a completely different neuronal sub-population with polymodal capabilities on the opposite mechanical modality spectrum (tactile). We have observed that several tactile afferents (1/5) can respond to cold in non-nociceptive ranges. These cells' mechanical thresholds and electrical properties are similar to any low-threshold mechano-receptors (LT), conducting in a broad range of velocities (Aδ to Aβ), lacking CGRP and TRPM8 receptors. Due to its density, cold-response range, speed, and response to injury (or lack thereof), we speculate on its role in controlling reflexive behaviors (wound liking and rubbing) and modulation of nociceptive spinal cord integration. Further studies are required to understand the mechanisms behind this neuron's polymodality, central architecture, and impact on pain perception.

触觉外周传入中同时存在机械和冷多模性,这并不是由 TRPM8 介导的。
在哺乳动物的躯体感觉系统中,多模态被定义为某些神经元能够对多种形式的能量(如机械能和热能)做出反应。这种能力被认为是痛觉神经元(多模式 C 纤维痛觉感受器)的独有特性,也是痛觉外周可塑性的支柱之一。目前的研究发现了一个完全不同的神经元亚群,它在相反的机械模态谱(触觉)上具有多模态能力。我们观察到,一些触觉传入细胞(1/5)可以在非痛觉范围内对寒冷做出反应。这些细胞的机械阈值和电特性与任何低阈值机械受体(LT)相似,传导速度范围广泛(Aδ至Aβ),缺乏CGRP和TRPM8受体。由于其密度、冷反应范围、速度和对损伤的反应(或无反应),我们推测其在控制反射行为(伤口喜好和摩擦)和调节脊髓痛觉整合中的作用。要了解这种神经元的多模式、中枢结构和对痛觉的影响,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Pain
Molecular Pain 医学-神经科学
CiteScore
5.60
自引率
3.00%
发文量
56
审稿时长
6-12 weeks
期刊介绍: Molecular Pain is a peer-reviewed, open access journal that considers manuscripts in pain research at the cellular, subcellular and molecular levels. Molecular Pain provides a forum for molecular pain scientists to communicate their research findings in a targeted manner to others in this important and growing field.
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