Takeda Mamoru, Oshima Katsuo, Takahashi Masayuki, Matsumoto Shigeji
Department of Physiology, School of Life Dentistry at Tokyo, Nippon Dental University, Tokyo, Japan.
Eur J Pain. 2009 Oct;13(9):929-34. doi: 10.1016/j.ejpain.2008.11.017. Epub 2008 Dec 31.
Although systemic lidocaine has been demonstrated to have analgesic actions in neuropathic pain conditions, the effect of intravenous lidocaine on trigeminal pain has not been elucidated. The aim of the present study is to investigate the effect of intravenous lidocaine administration on the excitability of the upper cervical dorsal horn (C1) neuron having convergent inputs from both tooth-pulp (TP) and facial skin as well as nociceptive jaw-opening reflex (JOR). After electrical stimulation of TP, extracellular single-unit recordings from 19 C1 neurons and the digastric muscle electromyogram (dEMG) were made in pentobarbital-anesthetized rats. These neurons also responded to non-noxious and noxious mechanical stimulation (touch and pinch) of facial skin, and every neuron was considered to be a wide dynamic range (WDR) neuron. The TP-evoked C1 neuronal and dEMG activities were dose-dependently inhibited by systematic administration of lidocaine (1-2 mg/kg, i.v.). After intravenous injection of lidocaine, the unit discharges induced by both touch and pinch stimuli were inhibited, and the size of the receptive field for pinch was also significantly decreased. The mean spontaneous discharge frequencies were significantly inhibited by the application of lidocaine. These changes were reversed within -20 min. These results suggest that in the absence of neuropathic pain intravenous lidocaine injection suppresses the trigeminal nociceptive reflex as well as the excitability of C1 neurons having convergent inputs from TP and somatic afferents. Systemic lidocaine administration, therefore, may contribute to the alleviation of trigeminal-referred pain associated with tooth pain.
尽管全身应用利多卡因已被证明在神经性疼痛状态下具有镇痛作用,但静脉注射利多卡因对三叉神经痛的影响尚未阐明。本研究的目的是探讨静脉注射利多卡因对来自牙髓(TP)和面部皮肤的汇聚输入以及伤害性张口反射(JOR)的上颈背角(C1)神经元兴奋性的影响。在对TP进行电刺激后,在戊巴比妥麻醉的大鼠中对19个C1神经元进行细胞外单单位记录,并记录二腹肌肌电图(dEMG)。这些神经元也对面部皮肤的非伤害性和伤害性机械刺激(触摸和捏)有反应,并且每个神经元都被认为是一个宽动态范围(WDR)神经元。TP诱发的C1神经元和dEMG活动被系统性给予利多卡因(1-2mg/kg,静脉注射)剂量依赖性地抑制。静脉注射利多卡因后,触摸和捏刺激诱发的单位放电均受到抑制,捏的感受野大小也显著减小。利多卡因的应用显著抑制了平均自发放电频率。这些变化在-20分钟内逆转。这些结果表明,在没有神经性疼痛的情况下,静脉注射利多卡因可抑制三叉神经伤害性反射以及来自TP和躯体传入的汇聚输入的C1神经元的兴奋性。因此,全身应用利多卡因可能有助于减轻与牙痛相关的三叉神经牵涉痛。