...
首页> 外文期刊>Molecular pain >Contribution of Piezo2 to endothelium-dependent pain
【24h】

Contribution of Piezo2 to endothelium-dependent pain

机译:Piezo2对内皮依赖性疼痛的贡献

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background We evaluated the role of a mechanically-gated ion channel, Piezo2, in mechanical stimulation-induced enhancement of hyperalgesia produced by the pronociceptive vasoactive mediator endothelin-1, an innocuous mechanical stimulus-induced enhancement of hyperalgesia that is vascular endothelial cell dependent. We also evaluated its role in a preclinical model of a vascular endothelial cell dependent painful peripheral neuropathy. Results The local administration of oligodeoxynucleotides antisense to Piezo2 mRNA, at the site of nociceptive testing in the rat’s hind paw, but not intrathecally at the central terminal of the nociceptor, prevented innocuous stimulus-induced enhancement of hyperalgesia produced by endothelin-1 (100 ng). The mechanical hyperalgesia induced by oxaliplatin (2 mg/kg. i.v.), which was inhibited by impairing endothelial cell function, was similarly attenuated by local injection of the Piezo2 antisense. Polymerase chain reaction analysis demonstrated for the first time the presence of Piezo2 mRNA in endothelial cells. Conclusions These results support the hypothesis that Piezo2 is a mechano-transducer in the endothelial cell where it contributes to stimulus-dependent hyperalgesia, and a model of chemotherapy-induced painful peripheral neuropathy.
机译:背景我们评估了机械门控离子通道Piezo2在机械刺激诱导的痛觉增强中的作用,痛觉感受性血管活性介质内皮素-1是一种无害的机械刺激诱导的痛觉增强,这是血管内皮细胞依赖性的。我们还评估了其在依赖血管内皮细胞的疼痛性周围神经病变的临床前模型中的作用。结果在大鼠后足的伤害感受测试部位而非伤害感受器中央末端鞘内局部施用针对Piezo2 mRNA反义的寡脱氧核苷酸可防止无害刺激诱导的内皮素-1(100 ng)痛觉过敏增强)。由奥沙利铂(2mg / kg.i.v。)诱导的机械性痛觉过敏被内皮细胞功能受损抑制,同样通过局部注射Piezo2反义物而减弱。聚合酶链反应分析首次证明内皮细胞中存在Piezo2 mRNA。结论这些结果支持以下假设:Piezo2是内皮细胞中的机械换能器,在其中它有助于刺激依赖性痛觉过敏,并且是化学疗法诱发的疼痛性周围神经病的模型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号