Objective: The leukotrienes are inflammatory mediators. In the present study, the analgesic role of local montelukast, a cysteinyl leukotriene receptor antagonist, and the possible involvement of L-arginine/NO/cGMP/KATP channel pathway and PPARγ receptors was assessed in the formalin test in rats.Methods and results: The local administration of montelukast into the hind paw produced dose-related analgesia during both phases of the formalin test. Furthermore, pre-treatment with L-NAME, methylene blue, and glibenclamide prevented montelukast (10 μg/paw)-induced antinociception in both early and late phases of the test. Moreover, the local L-arginine and diazoxide before the sub-effective dose of montelukast (3 μg/paw) produced an analgesic effect. Also, local GW-9662 blocked antinociception induced by montelukast plus pioglitazone (10 μg/paw).Conclusion: In conclusion, montelukast produced peripheral analgesia through PPARγ receptors and activation of the L-arginine/NO/cGMP/KATP channel pathway, with potential for a new topical analgesic drug.

译文

目的: 白三烯是炎症介质。在本研究中,在大鼠福尔马林试验中评估了局部孟鲁司特 (半胱氨酰白三烯受体拮抗剂) 的镇痛作用以及L-精氨酸/NO/cGMP/KATP通道途径和ppar γ 受体的可能参与。方法和结果: 在福尔马林试验的两个阶段,将孟鲁司特局部施用到后爪中会产生剂量相关的镇痛作用。此外,在试验的早期和晚期,用L-NAME,亚甲蓝和格列本脲进行预处理可防止孟鲁司特 (10 μ g/paw) 诱导的抗伤害感受。此外,在次有效剂量孟鲁司特 (3  μ g/paw) 之前,局部L-精氨酸和二氮嗪产生镇痛作用。此外,局部GW-9662阻断了孟鲁司特联合吡格列酮 (10 μ g/paw) 诱导的抗伤害感受。结论: 孟鲁司特通过ppar γ 受体和L-精氨酸/NO/cGMP/KATP通道通路的激活产生外周镇痛作用,有可能成为一种新的局部镇痛药物。

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