Costentin J
Unité de Neuropsychopharmacologie Expérimentale, ESA 6036 CNRS, Institut Fédératif de Recherches Multidisciplinaires sur les Peptides=IFR 23, Faculté de Médecine et Pharmacie, 22, bd Gambetta, F 76000 Rouen.
Ann Pharm Fr. 2000 Mar;58(2):77-83.
The pain message originates peripherally from a great variety of substances either released from preformed stores or extemporaneously synthetized. They stimulate or sensitize nociceptors which are associated with the peripheral endings of sensitive protoneurones. Their central endings release many types of transmitters in the dorsal horn of medulla (substance P, NO, CGRP.). At this level their release, triggered by the firing rate, is modulated by the stimulation of various presynaptic receptors operated by transmitters produced by either interneurones (enkephalins) or medullar descending neurons (dopamine, norepinephrine, serotonine). These modulations correspond to the so-called gate control. The sensitive consecutive neurones which climb towards various brain areas are submitted to contradictory influences. Several of them enhance the pain perception (nociceptin, cholecystokinin, neuropeptide FF.) whereas several other reduce it (endorphines, neurotensin, neuromedin N, anandamide.).
疼痛信号在外周源自多种物质,这些物质要么从预先形成的储存库中释放,要么是临时合成的。它们刺激或致敏伤害感受器,这些感受器与感觉初级神经元的外周末梢相关联。它们的中枢末梢在延髓背角释放多种类型的递质(P物质、一氧化氮、降钙素基因相关肽)。在此水平,它们的释放由放电频率触发,并受到由中间神经元(脑啡肽)或延髓下行神经元(多巴胺、去甲肾上腺素、5-羟色胺)产生的递质所操作的各种突触前受体刺激的调节。这些调节对应于所谓的闸门控制。向不同脑区上行的敏感连续神经元受到相互矛盾的影响。其中一些增强痛觉(孤啡肽、胆囊收缩素、神经肽FF),而其他一些则减轻痛觉(内啡肽、神经降压素、神经介素N、花生四烯乙醇胺)。