Davidson E M, Coggeshall R E, Carlton S M
Department of Anatomy and Neurosciences, Marine Biomedical Institute, Galveston, TX 77555-1069, USA.
Neuroreport. 1997 Mar 3;8(4):941-6. doi: 10.1097/00001756-199703030-00025.
The present study demonstrates that local cutaneous administration of either the N-methyl-D-aspartate (NMDA) glutamate receptor antagonist MK-801 or the non-NMDA glutamate receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) significantly attenuates formalin-induced nociceptive behaviors. Specifically, pretreatment with either drug reduced the magnitude and time course of lifting and licking behavior in the late phase of formalin pain; however, flinching behavior was not affected. In contrast, post-treatment of formalin pain with either antagonist did not affect lifting and licking behavior, although flinching behavior was mildly attenuated. We hypothesize that these actions result from blocking of peripheral glutamate receptors located on unmyelinated axons at the dermal-epidermal junction. These data suggest that peripheral glutamate receptors on cutaneous axons can be manipulated to reduce certain aspects of pain of peripheral origin. This route of administration offers the advantage of avoiding the side effects of systemic administration.
本研究表明,局部皮肤给予N-甲基-D-天冬氨酸(NMDA)谷氨酸受体拮抗剂MK-801或非NMDA谷氨酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)均可显著减轻福尔马林诱导的伤害性行为。具体而言,两种药物预处理均可降低福尔马林疼痛后期抬举和舔舐行为的程度及时程;然而,惊跳行为未受影响。相比之下,两种拮抗剂对福尔马林疼痛进行治疗后,虽惊跳行为略有减轻,但抬举和舔舐行为未受影响。我们推测,这些作用是由于阻断了位于真皮-表皮交界处无髓鞘轴突上的外周谷氨酸受体所致。这些数据表明,可通过操纵皮肤轴突上的外周谷氨酸受体来减轻外周源性疼痛的某些方面。这种给药途径具有避免全身给药副作用的优势。