冷痛的分子机制

Q2 Medicine
Donald Iain MacDonald , John N. Wood, Edward C. Emery
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引用次数: 32

摘要

冷却的感觉是生存所必需的。极度寒冷是一种有害的刺激,它会驱动保护行为,因此我们将其视为疼痛。然而,慢性疼痛患者遭受冷异常性疼痛矛盾地经历无害的冷却作为痛苦的疼痛。感知温度下降的外周感觉神经元表达许多冷敏感和电压门控离子通道,这些通道控制着它们在健康和疾病中对冷却的反应。在这篇综述中,我们讨论了这些离子通道如何在生理条件下控制冷感和冷痛,然后重点讨论了离子通道触发病理性冷痛的分子机制。随着慢性疼痛患者数量的不断增加,我们最后强调了迫切需要确定参与冷异常性疼痛的细胞和分子,从而确定新的、合理的冷痛镇痛药物靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular mechanisms of cold pain

Molecular mechanisms of cold pain

Molecular mechanisms of cold pain

Molecular mechanisms of cold pain

The sensation of cooling is essential for survival. Extreme cold is a noxious stimulus that drives protective behaviour and that we thus perceive as pain. However, chronic pain patients suffering from cold allodynia paradoxically experience innocuous cooling as excruciating pain. Peripheral sensory neurons that detect decreasing temperature express numerous cold-sensitive and voltage-gated ion channels that govern their response to cooling in health and disease. In this review, we discuss how these ion channels control the sense of cooling and cold pain under physiological conditions, before focusing on the molecular mechanisms by which ion channels can trigger pathological cold pain. With the ever-rising number of patients burdened by chronic pain, we end by highlighting the pressing need to define the cells and molecules involved in cold allodynia and so identify new, rational drug targets for the analgesic treatment of cold pain.

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来源期刊
Neurobiology of Pain
Neurobiology of Pain Medicine-Anesthesiology and Pain Medicine
CiteScore
4.40
自引率
0.00%
发文量
29
审稿时长
54 days
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