Petrenko Andrei B, Yamakura Tomohiro, Baba Hiroshi, Shimoji Koki
From the Department of Anesthesiology, Niigata University School of Medicine, Asahimachi 1-757, Niigata 951-8510, Japan.
Anesth Analg. 2003 Oct;97(4):1108-1116. doi: 10.1213/01.ANE.0000081061.12235.55.
There is accumulating evidence to implicate the importance of N-methyl-D-aspartate (NMDA) receptors to the induction and maintenance of central sensitization during pain states. However, NMDA receptors may also mediate peripheral sensitization and visceral pain. NMDA receptors are composed of NR1, NR2 (A, B, C, and D), and NR3 (A and B) subunits, which determine the functional properties of native NMDA receptors. Among NMDA receptor subtypes, the NR2B subunit-containing receptors appear particularly important for nociception, thus leading to the possibility that NR2B-selective antagonists may be useful in the treatment of chronic pain.
越来越多的证据表明,N-甲基-D-天冬氨酸(NMDA)受体在疼痛状态下对中枢敏化的诱导和维持具有重要作用。然而,NMDA受体也可能介导外周敏化和内脏疼痛。NMDA受体由NR1、NR2(A、B、C和D)以及NR3(A和B)亚基组成,这些亚基决定了天然NMDA受体的功能特性。在NMDA受体亚型中,含NR2B亚基的受体对伤害感受显得尤为重要,因此,NR2B选择性拮抗剂可能对慢性疼痛的治疗有用。