Molecular basis of pain: Membrane receptors involved in pain

Claudia I. Gutiérrez-Román
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Abstract

Pain is the most commonly reported symptom by both adult and pediatric patients, the International Association for the Study of Pain (IASP) defines pain as "An unpleasant sensory and emotional experience associated with, or similar to that associated with, actual tissue damage or potential. Pain can have a significant negative impact on quality of life in the context of human disease, in temporality physiological pain is usually acute and pathological pain is usually chronic. Nociceptors are specialized nerve fibers for pain, they are found in the skin, organ of movement, they are classified as myelin fibers that are called Aδ; and unmyelinated fibers or C fibers. Nociceptors can be stimulated by biological agents, electrical, thermal, mechanical and chemical stimuli, once the stimulus is received it will be transmitted to the brain. One of the pillars of anesthesia is analgesia, that is to say, inhibiting pain. In this bibliographic review, the aim is to explain the molecular bases, emphasizing the main membrane receptors activated in the presence of pain.
疼痛的分子基础:参与疼痛的膜受体
疼痛是成人和儿科患者最常报告的症状,国际疼痛研究协会(IASP)将疼痛定义为“与实际组织损伤或潜在组织损伤相关或类似的不愉快的感觉和情绪体验。”在人类疾病的背景下,疼痛可以对生活质量产生重大的负面影响,在暂时的生理性疼痛通常是急性的,而病理性疼痛通常是慢性的。痛觉感受器是专门用于疼痛的神经纤维,它们存在于皮肤和运动器官中,它们被归类为髓鞘纤维,称为Aδ;和无髓鞘纤维或C纤维。伤害感受器可以受到生物制剂、电刺激、热刺激、机械刺激和化学刺激的刺激,一旦受到刺激就会传递到大脑。麻醉的支柱之一是镇痛,也就是说,抑制疼痛。在这篇文献综述中,目的是解释分子基础,强调在疼痛存在时激活的主要膜受体。
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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