首页    期刊浏览 2025年03月01日 星期六
登录注册

文章基本信息

  • 标题:TRPV1 channels and the progesterone receptor Sig-1R interact to regulate pain
  • 本地全文:下载
  • 作者:Miguel Ortíz-Rentería ; Rebeca Juárez-Contreras ; Ricardo González-Ramírez
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2018
  • 卷号:115
  • 期号:7
  • 页码:E1657-E1666
  • DOI:10.1073/pnas.1715972115
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:The Transient Receptor Potential Vanilloid 1 (TRPV1) ion channel is expressed in nociceptors where, when activated by chemical or thermal stimuli, it functions as an important transducer of painful and itch-related stimuli. Although the interaction of TRPV1 with proteins that regulate its function has been previously explored, their modulation by chaperones has not been elucidated, as is the case for other mammalian TRP channels. Here we show that TRPV1 physically interacts with the Sigma 1 Receptor (Sig-1R), a chaperone that binds progesterone, an antagonist of Sig-1R and an important neurosteroid associated to the modulation of pain. Antagonism of Sig-1R by progesterone results in the down-regulation of TRPV1 expression in the plasma membrane of sensory neurons and, consequently, a decrease in capsaicin-induced nociceptive responses. This is observed both in males treated with a synthetic antagonist of Sig-1R and in pregnant females where progesterone levels are elevated. This constitutes a previously undescribed mechanism by which TRPV1-dependent nociception and pain can be regulated.
  • 关键词:TRPV1 ; chaperone ; pain ; sigma 1 receptor ; progesterone
国家哲学社会科学文献中心版权所有