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Influence of NMDA and non-NMDA antagonists on acute and inflammatory pain in the trigeminal territory: a placebo control study

机译:NMDA和非NMDA拮抗剂对三叉神经急性和炎性疼痛的影响:安慰剂对照研究

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NMDA and non-NMDA receptors are involved in spinal transmission of nociceptive information in physiological and pathological conditions. Our objective was to study the influence of NMDA and non-NMDA receptor antagonists on pain control in the trigeminal system using a formalin-induced orofacial pain model. Motor performance was also evaluated. Male Rattus norvegicus were pre-treated with topiramate (T) (n=8), memantine (M) (n=8), divalproex (D) (n=8) or isotonic saline solution (ISS) (n=10) intraperitoneally 30 minutes before the formalin test. Formalin 2.5% was injected into the right upper lip (V2 branch) and induced two phases: phase I (early or neurogenic) (0-3 min) and phase II (late or inflammatory) (12-30 min). For motor behavior performance we used the open-field test and measured latency to movement onset, locomotion and rearing frequencies, and immobility time. Pre-treatment of animals with M and D only attenuated nociceptive formalin behavior for phase II. T increased locomotion and rearing frequencies and reduced immobility time. Treatment with M increased immobility time and with D reduced locomotion frequency. Our results showed that the NMDA antagonist (M) is more potent than the non-NMDA antagonists (D and T) in the control of pain in the inflammatory phase. The non-NMDA topiramate improved motor performance more than did D and M, probably because T has more anxiolytic properties.
机译:NMDA和非NMDA受体在生理和病理条件下参与伤害性信息的脊柱传递。我们的目标是使用福尔马林诱导的口腔颌面疼痛模型研究NMDA和非NMDA受体拮抗剂对三叉神经系统疼痛控制的影响。还评估了电机性能。雄性褐家鼠经腹膜内用托吡酯(T)(n = 8),美金刚(M)(n = 8),双丙戊酸钠(D)(n = 8)或等渗盐溶液(ISS)(n = 10)进行腹膜前处理福尔马林测试前30分钟。将2.5%的福尔马林注射到右上唇(V2分支)中,并诱导两个阶段:I期(早期或神经性)(0-3分钟)和II期(晚期或发炎)(12-30分钟)。对于运动行为表现,我们使用了野外测试,并测量了运动开始,运动和饲养频率以及不动时间的潜伏期。用M和D预处理动物只会减弱II期的伤害性福尔马林行为。 T增加了运动和饲养频率并减少了不动时间。用M治疗增加了不动时间,而用D治疗减少了运动频率。我们的结果表明,NMDA拮抗剂(M)在控制炎症期疼痛方面比非NMDA拮抗剂(D和T)更有效。非NMDA托吡酯比D和M改善的运动性能更多,可能是因为T具有更多的抗焦虑特性。

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