清络通痹方对小鼠疼痛行为及DRG中COX-2表达和血PGE2的影响

Effects of Qingluo Tongbi Compound on Pain Behavior and Expression of COX-2 in Dorsal Root Ganglion and Blood PGE2

  • 摘要: 目的 观察清络通痹方对疼痛模型和胶原关节炎(CIA)小鼠模型的疼痛行为的影响,及背根神经节(DRG)环氧合酶(COX)-2 mRNA及血前列腺素E2(PGE2)含量的影响,初步探讨清络通痹方干预类风湿关节炎疼痛的作用及可能机制。方法 采用热板和醋酸扭体致痛模型,分为空白对照组、塞来昔布组(30mg/kg)、清络通痹低剂量组(4.35g/kg)、中剂量组(8.70g/kg)、高剂量组(17.4g/kg),观察各组痛阈值和扭体次数的改变。DBA/1小鼠,复制CIA模型,随机分为空白对照组、模型组、清络通痹方组(8.7g/kg)及塞来昔布组(30mg/kg),观察一般情况及关节肿胀,各组机械缩足反射阈值(MWT)和热缩足反射阈值(TWL)的变化,灌胃给药4周后,检测DRG COX-2 mRNA及血清PGE2含量。结果 清络通痹方使小鼠热板法致痛模型痛阈值提高、醋酸扭体法致痛模型扭体次数减少(P<0.01);可显著减轻CIA小鼠足肿胀(P<0.05),提高其MWT(P<0.01)和PWL(P<0.05)阈值,降低DRG中COX-2 mRNA的表达(P<0.05)和血PGE2的含量(P<0.05)。结论 清络通痹方具有一定的镇痛作用,其镇痛机制可能与抑制DRG中COX-2 mRNA表达和血清中PGE2含量相关。

     

    Abstract: OBJECTIVE To study the effects of Qingluo Tongbi Compound(QLT) on pain behavior and COX-2 mRNA expression in dorsal root ganglion(DRG) and blood PGE2 concentration, and to explore the mechanisms of pain in rheumatoid arthritis. METHODS The mice were randomly divided into control group, celecoxib 30mg/kg,QLT 4.35g/kg, QLT 8.70g/kg and QLT 17.4g/kg groups. The mice pain threshold change were measured by hot plate method, and body torsion times were tested by acetic acid twisting method. The collagen-induced arthritis(CIA) was induced by collagenⅡ in DBA/1 mice. The mice were randomly divided into control group, CIA group, celecoxib 30mg/kg group, QLT 8.70g/kg. The paws swelling, mechanical withdrawal threshold(MWT) and thermal withdrawal latency(TWL) were recorded. After treated with corresponding drugs by intragastric administration for four weeks, COX-2 mRNA in DRG and PGE2 in mice were quantified. RESULTS QLT reduced pain threshold and body torsion times in pain model mice(P<0.01); compared with the CIA group, the QLT group decreased the paws swelling(P<0.05), up-regulated MWT(P<0.01) and PWL(P<0.05), down-regulated the expression level of COX-2 mRNA in DRG and PGE2 concentrations in blood. CONCLUSION QLT shows certain analgesic action, which might be related to the inhibitory effect of COX-2 mRNA expression in DRG and PGE2 in blood.

     

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