Liebeskind J C, Sherman J E, Cannon T
Anaesth Intensive Care. 1982 May;10(2):139-43. doi: 10.1177/0310057X8201000209.
Recent studies which suggest the existence of an endogenous neural substrate of pain inhibition are reviewed. Electrical stimulation of some areas of the medial brain stem in laboratory rats has produced a dramatic degree of analgesia. Such stimulation-produced analgesia is partially blocked by an opiate antagonist drug. This observation has proved seminal to those searching for endogenous opiate-like neurochemicals, the opioid peptides (enkephalins and endorphins). Particular attention is focused on studies of stimulation-produced analgesia, the underlying anatomy and physiology of endogenous analgesia systems elucidated by such work, and the relation of these findings to discoveries about opiate receptors and opioid peptides. Very recent work suggesting that certain forms of stress are natural triggers for activating endogenous analgesia mechanisms is described. Although certain stressors cause analgesia mediated by opioids, other stressors cause analgesia by neurochemically different means. Thus, multiple analgesia substrates, opioid and nonopioid, appear to exist.
本文综述了近期一些表明存在内源性疼痛抑制神经基质的研究。对实验大鼠中脑内侧某些区域进行电刺激已产生显著程度的镇痛效果。这种电刺激产生的镇痛作用部分被阿片拮抗剂药物阻断。这一观察结果对于寻找内源性阿片样神经化学物质——阿片肽(脑啡肽和内啡肽)的研究人员来说具有开创性意义。本文特别关注对电刺激产生的镇痛作用的研究、通过此类研究阐明的内源性镇痛系统的基础解剖学和生理学,以及这些发现与阿片受体和阿片肽发现之间的关系。文中还描述了最近的研究工作,这些研究表明某些形式的应激是激活内源性镇痛机制的自然触发因素。尽管某些应激源会导致由阿片类物质介导的镇痛作用,但其他应激源通过神经化学方式不同的手段导致镇痛。因此,似乎存在多种镇痛基质,包括阿片类和非阿片类。