疼痛,疼痛缓解机制和创伤

B. Sjolund
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引用次数: 0

摘要

痛觉神经纤维的活动不仅会引发痛觉,而且还会启动各种有害反射,以保护生物体免受有害物质的伤害。如果这些反射活动的时间足够长,其中一些反射本身可能是有害的,引起内脏器官缺血或其他无意的反应。近年来,一些内源性机制被发现可以抑制神经冲动从伤害性传入神经细胞向其他神经细胞的传递,从而既阻止痛觉,又调节伤害性反射反应。一些这样的机制可能涉及内啡肽的释放。这是一种小肽,具有类似鸦片的活性,1975年由英国的休斯和科斯特利茨以及瑞典的特雷尼乌斯首次发现。这种内啡肽在中枢神经系统中的分布是由Hökfelt和他的同事首先研究的。从伤害感觉的角度来看,他们在几个感兴趣的领域发现了含有内啡肽的终末和细胞体。因此脊髓背角、第五脑神经的相应区域和导水管周围灰质都含有这种物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pain, Painrelieving Mechanisms and Trauma
Activity in nociceptive nerve fibers does not only trigger the sensation of pain but it also starts a variety of nocifensive reflexes to protect the organism from the noxious agent. Some of these reflexes may, if active long enough, be harmful themselves, causing ischemia in visceral organs or other inadvertent reactions. Recently, several endogenous mechanisms have been discovered that can inhibit the transmission of nerve impulses from nociceptive afferents to other nerve cells, thus not only preventing the pain sensation but also modulating the nocifensive reflex responses. Several such mechanisms may involve the release of endorphins. These are small peptides, with opiate-like activity that were first discovered in 1975 by Hughes and Kosterlitz in Great Britain and by Terenius in Sweden. The distribution of such endorphins in the central nervous system was first investigated by Hökfelt and his coworkers. They found terminals and cell bodies containing endorphins in several areas of interest from the point of view of nociception. Thus the dorsal horn of the spinal cord, the corresponding area of the fifth cranial nerve and the periaqueductal gray matter contained such material.
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