Fujimi Yoshinobu, Takeda Mamoru, Tanimoto Takeshi, Matsumoto Shigeji
Department of Physiology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-ku, Tokyo, 102-8159, Japan,
Odontology. 2006 Sep;94(1):22-8. doi: 10.1007/s10266-006-0057-1.
The aim of the present study was to determine whether there is a convergence of inputs from tooth pulp (TP) and the superior sagittal sinus (SSS) on rat C1 spinal neurons, and to examine the effects of iontophoretically applied N-methyl-D: -aspartate (NMDA) and non-NMDA receptor antagonists on the SSS-evoked activity of C1 neurons. Extracellular single unit-recordings were made from 20 C1 units responding to TP electrical stimulation with a constant temporal relationship to a digastric electromyogram signal, using a multibarrel electrode in pentobarbital-anesthetized rats. Ninety percent of C1 neurons (18/20) responding to TP stimulation also responded to the SSS stimulation. These neurons were considered to be SSS-afferent inputs from Adelta-fibers (5.8 +/- 0.6 m/s; n = 18), based on the calculation of nerve conduction velocity. After the iontophoretic application (30, 50, and 70 nA) of an NMDA receptor blocker (5R-10S)-(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d] cycloheptene-5,10-imine hydrogen maleate (MK801) or a non-NMDA receptor blocker (6-cyano-7-nitroquinoxaline-2,3-dione) (CNQX), the mean number of spikes responding to the SSS stimulation significantly decreased (30, 50, and 70 nA; P < 0.05). These results suggest that there is a convergence of inputs from SSS and TP afferents on C1 neurons; it is possible that both NMDA and non-NMDA receptors located on C1 neurons may be targets for the treatment of the trigeminal referred pain associated with migraine.
本研究的目的是确定来自牙髓(TP)和上矢状窦(SSS)的输入是否在大鼠C1脊髓神经元上汇聚,并研究离子导入N-甲基-D-天冬氨酸(NMDA)和非NMDA受体拮抗剂对C1神经元SSS诱发活动的影响。在戊巴比妥麻醉的大鼠中,使用多管电极从20个与二腹肌肌电图信号具有恒定时间关系且对TP电刺激有反应的C1单位进行细胞外单单位记录。对TP刺激有反应的C1神经元中有90%(18/20)也对SSS刺激有反应。根据神经传导速度的计算,这些神经元被认为是来自Aδ纤维(5.8±0.6米/秒;n = 18)的SSS传入输入。在离子导入NMDA受体阻滞剂(5R-10S)-(+)-5-甲基-10,11-二氢-5H-二苯并[a,d]环庚烯-5,10-亚胺马来酸氢盐(MK801)或非NMDA受体阻滞剂(6-氰基-7-硝基喹喔啉-2,3-二酮)(CNQX)(30、50和70纳安)后,对SSS刺激有反应的平均尖峰数量显著减少(30、50和70纳安;P < 0.05)。这些结果表明,SSS和TP传入在C1神经元上存在输入汇聚;位于C1神经元上的NMDA和非NMDA受体都有可能成为治疗与偏头痛相关的三叉神经牵涉痛的靶点。