首页> 外文期刊>Behavioural Brain Research: An International Journal >Topical application of L-menthol induces heat analgesia, mechanical allodynia, and a biphasic effect on cold sensitivity in rats.
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Topical application of L-menthol induces heat analgesia, mechanical allodynia, and a biphasic effect on cold sensitivity in rats.

机译:L-薄荷醇的局部应用可引起大鼠热镇痛,机械性异常性疼痛以及对冷敏感的双相效应。

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摘要

Menthol is used in analgesic balms and also in foods and oral hygiene products for its fresh cooling sensation. Menthol enhances cooling by interacting with the cold-sensitive thermoTRP channel TRPM8, but its effect on pain is less well understood. We presently used behavioral methods to investigate effects of topical menthol on thermal (hot and cold) pain and innocuous cold and mechanical sensitivity in rats. Menthol dose-dependently increased the latency for noxious heat-evoked withdrawal of the treated hindpaw with a weak mirror-image effect, indicating antinociception. Menthol at the highest concentration (40%) reduced mechanical withdrawal thresholds, with no effect at lower concentrations. Menthol had a biphasic effect on cold avoidance. At high concentrations (10% and 40%) menthol reduced avoidance of colder temperatures (15 degrees C and 20 degrees C) compared to 30 degrees C, while at lower concentrations (0.01-1%) menthol enhanced cold avoidance. In a -5 degrees C cold plate test, 40% menthol significantly increased the nocifensive response latency (cold hypoalgesia) while lower concentrations were not different from vehicle controls. These results are generally consistent with neurophysiological and human psychophysical data and support TRPM8 as a potential peripheral target of pain modulation.
机译:薄荷醇因其清新的凉爽感而被用于止痛膏以及食品和口腔卫生产品中。薄荷醇通过与冷敏感的thermoTRP通道TRPM8相互作用来增强冷却作用,但其对疼痛的作用尚不十分清楚。我们目前使用行为方法来研究局部薄荷醇对大鼠的热(热和冷)痛以及无害的冷和机械敏感性的影响。薄荷醇剂量依赖性地增加了经治疗的后足进行有害的热诱发撤药的潜伏期,具有微弱的镜像效应,表明抗伤害感受。最高浓度(40%)的薄荷醇降低了机械退缩阈值,较低浓度无作用。薄荷醇对避免感冒具有两相作用。在高浓度(10%和40%)下,薄荷醇与30摄氏度相比降低了对较低温度(15摄氏度和20摄氏度)的避免,而在较低浓度(0.01-1%)下,薄荷醇增强了对寒冷的避免。在-5°C的冷板测试中,40%的薄荷醇显着增加了伤害反应潜伏期(冷痛觉过敏),而较低的浓度与载体对照组无差异。这些结果通常与神经生理学和人类心理物理数据一致,并支持TRPM8作为疼痛调节的潜在外周靶标。

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