脑内注射白介素- 1 β对自由活动大鼠急性和炎症性口面部疼痛模型的差异反应

H. Choi, J. S. Park, D. Ahn
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引用次数: 5

摘要

本研究以自由运动大鼠为实验对象,通过伤害性张开颌反射和口面部福尔马林试验,探讨某些白细胞介素-1β在伤害性中的调节作用。在急性疼痛模型中,腹腔注射10 pg、100 pg和1 ng IL-1β均未改变二腹肌电图(dEMG)。然而,10 ng IL-1β抑制dEMG至控制值的76±8%。在炎症性疼痛模型中,腹腔注射10 pg IL-1β不会改变福尔马林诱导的有害行为反应。然而,100 pg IL-1β增加了福尔马林诱导的有害行为反应。在高剂量10 ng IL-1β时,不增加福尔马林诱导的行为反应。IL-1受体拮抗剂预处理可消除100pg IL-1β的过敏反应。这些结果表明,内胆注射IL-1β可调节口面区伤害性信息的传递。中枢细胞因子的低/高痛觉反应似乎依赖于疼痛模型或剂量相关方式,高痛觉作用似乎是由IL-1受体介导的。
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Differential responses of intracisternal injection of interleukin‐1 β to acute and inflammatory orofacial pain model in freely moving rats
The present study was performed to investigate the modulatory role of certain interleukin (IL)-1β in nociception with a nociceptive jaw opening reflex and an orofacial formalin test in freely moving rats. In an acute pain model, 10 pg, 100 pg and 1 ng IL-1β injected intracisternally did not change the digastric eletromyogram (dEMG). However, 10 ng IL-1β suppressed dEMG to 76±8 % of control values. In an inflammatory pain model, 10 pg IL-1β injected intracisternally did not change formalin-induced noxious behavioral responses. However, 100 pg IL-1β increased formalin-induced noxious behavioral responses. At higher dose of 10 ng IL-1β, it did not increase formalin-induced behavioral responses. Pretreatment with IL-1 receptor antagonist abolished hyperalgesic response of 100 pg IL-1β. These results suggest that the intracisternal injection of IL-1β modulate the transmission of nociceptive information in the orofacial area. The hypo/hyper-algesic responses of central cytokines seem to depend on the pain model or dose related manner and the hyperalgesic action seems to be mediated by IL-1 receptor.
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