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N-甲基-D-天冬氨酸(NMDA)和非NMDA受体拮抗剂可抑制大鼠中由上矢状窦诱发的、对牙髓电刺激产生反应的C1脊髓神经元的活动。

N-methyl-D-aspartate (NMDA) and non-NMDA receptor antagonists suppress the superior sagittal sinus-evoked activity of C1 spinal neurons responding to tooth pulp electrical stimulation in rats.

作者信息

Fujimi Yoshinobu, Takeda Mamoru, Tanimoto Takeshi, Matsumoto Shigeji

机构信息

Department of Physiology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-ku, Tokyo, 102-8159, Japan,

出版信息

Odontology. 2006 Sep;94(1):22-8. doi: 10.1007/s10266-006-0057-1.

Abstract

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.

摘要

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。

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