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一种“牙痛树”酰胺抑制 Aδ 机械伤害感受器,缓解机械性疼痛。

A 'toothache tree' alkylamide inhibits Aδ mechanonociceptors to alleviate mechanical pain.

机构信息

Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA 94720, USA.

出版信息

J Physiol. 2013 Jul 1;591(13):3325-40. doi: 10.1113/jphysiol.2013.252106. Epub 2013 May 7.

Abstract

In traditional medicine, the 'toothache tree' and other plants of the Zanthoxylum genus have been used to treat inflammatory pain conditions, such as toothache and rheumatoid arthritis. Here we examined the cellular and molecular mechanisms underlying the analgesic properties of hydroxy-α-sanshool, the active alkylamide produced by Zanthoxylum plants. Consistent with its analgesic effects in humans, sanshool treatment in mice caused a selective attenuation of mechanical sensitivity under naïve and inflammatory conditions, with no effect on thermal sensitivity. To elucidate the molecular mechanisms by which sanshool attenuates mechanical pain, we performed single fibre recordings, calcium imaging and whole-cell electrophysiology of cultured sensory neurons. We found that: (1) sanshool potently inhibits Aδ mechanonociceptors that mediate both sharp acute pain and inflammatory pain; (2) sanshool inhibits action potential firing by blocking voltage-gated sodium currents in a subset of somatosensory neurons, which express a unique combination of voltage-gated sodium channels; and (3) heterologously expressed Nav1.7 is most strongly inhibited by sanshool as compared to other sodium channels expressed in sensory neurons. These results suggest that sanshool targets voltage-gated sodium channels on Aδ mechanosensory nociceptors to dampen excitability and thus induce 'fast pain' analgesia.

摘要

在传统医学中,“牙痛树”和花椒属的其他植物被用于治疗炎症性疼痛,如牙痛和类风湿关节炎。在这里,我们研究了羟基-α-山椒素的镇痛特性的细胞和分子机制,羟基-α-山椒素是花椒属植物产生的活性烷基酰胺。与它在人类中的镇痛作用一致,山椒素处理在小鼠中引起了在未致敏和炎症条件下机械敏感性的选择性衰减,对热敏感性没有影响。为了阐明山椒素减轻机械性疼痛的分子机制,我们对培养的感觉神经元进行了单纤维记录、钙成像和全细胞膜片钳电生理学研究。我们发现:(1)山椒素强烈抑制介导锐痛和炎症痛的 Aδ机械伤害感受器;(2)山椒素通过阻断一组感觉神经元中的电压门控钠电流来抑制动作电位的发放,这些神经元表达独特的电压门控钠通道组合;(3)与在感觉神经元中表达的其他钠通道相比,Nav1.7 被山椒素抑制的程度最强。这些结果表明,山椒素靶向 Aδ机械伤害感受器上的电压门控钠通道,以抑制兴奋性,从而诱导“快痛”镇痛。

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