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Coapplication of Lidocaine and Membrane-Impermeable Lidocaine Derivative QX-222 Produces Divergent Effects on Evoked and Spontaneous Nociceptive Behaviors in Mice

机译:利多卡因和膜不渗透性利多卡因衍生物QX-222的共同应用对小鼠诱发的和自发的伤害行为产生不同的作用

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摘要

The present study was aimed at investigating the analgesic properties of a combination of lidocaine and QX-222 and its effects on evoked pain behavior (complete Freund's adjuvant-induced allodynia and hyperalgesia in inflammatory condition) and spontaneous pain behavior (formalin-induced acute pain) in mice. Drugs were injected adjacent to sciatic nerve or into plantar. Motor function, thermal withdrawal latency, mechanical withdrawal threshold, and licking/biting were evaluated by behavioral tests. A combination of lidocaine and QX-222 adjacent sciatic nerve injection produced the long-lasting sensory-specific nerve block, and intraplantar injection inhibited spontaneous pain in the formalin-treated mice but did not detectably attenuated hyperalgesia and allodynia in the complete Freund's adjuvant- (CFA-) treated mice. Our results suggest that a combination of lidocaine and QX-222 achieves a long-lasting differential block (sensory selective) and produces divergent effects on evoked and spontaneous pain behaviors in mice.
机译:本研究旨在研究利多卡因和QX-222组合的镇痛特性及其对诱发的疼痛行为(炎症状态下完全弗氏佐剂引起的异常性疼痛和痛觉过敏)和自发性疼痛行为(福尔马林引起的急性疼痛)的影响在小鼠中。将药物注射到坐骨神经附近或足底。通过行为测试评估运动功能,热退缩潜伏期,机械退缩阈值和舔/咬。利多卡因和QX-222相邻坐骨神经注射的组合产生了持久的感觉特异性神经阻滞,而足底注射抑制了福尔马林处理的小鼠的自发性疼痛,但在完整的弗氏佐剂中未检测到减轻痛觉过敏和异常性疼痛-( CFA-)处理的小鼠。我们的结果表明,利多卡因和QX-222的组合可实现持久的差异阻滞作用(感觉选择性),并对小鼠诱发的和自发的疼痛行为产生不同的影响。

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