Behavioral phenotypes of mice lacking purinergic P2X4 receptors in acute and chronic pain assays

Makoto Tsuda, Kazuya Kuboyama, Tomoyuki Inoue, Kenichiro Nagata, Hidetoshi Tozaki-Saitoh, Kazuhide Inoue

研究成果: Contribution to journalArticle査読

135 被引用数 (Scopus)

抄録

A growing body of evidence indicates that P2X receptors (P2XRs), a family of ligand-gated cation channels activated by extracellular ATP, play an important role in pain signaling. In contrast to the role of the P2X3R subtype that has been extensively studied, the precise roles of others among the seven P2XR subtypes (P2X1 R-P2X7R) remain to be determined because of a lack of sufficiently powerful tools to specifically block P2XR signaling in vivo. In the present study, we investigated the behavioral phenotypes of a line of mice in which the p2rx4 gene was disrupted in a series of acute and chronic pain assays. While p2rx4-/- mice showed no major defects in pain responses evoked by acute noxious stimuli and local tissue damage or in motor function as compared with wild-type mice, these mice displayed reduced pain responses in two models of chronic pain (inflammatory and neuropathic pain). In a model of chronic inflammatory pain developed by intraplantar injectin of complete Freund's adjuvant (CFA), p2rx4-/- mice exhibited attenuations of pain hypersensitivity to innocuous mechanical stimuli (tactile allodynia) and also of the CFA-induced swelling of the hindpaw. A most striking phenotype was observed in a test of neuropathic pain: tactile allodynia caused by an injury to spinal nerve was markedly blunted in p2rx4-/- mice. By contrast, pain hypersensitivity to a cold stimulus (cold allodynia) after the injury was comparable in wild-type and p2rx4-/- mice. Together, these findings reveal a predominant contribution of P2X4R to nerve injury-induced tactile allodynia and, to the lesser extent, peripheral inflammation. Loss of P2X4R produced no defects in acute physiological pain or tissue damaged-induced pain, highlighting the possibility of a therapeutic benefit of blocking P2X4R in the treatment of chronic pain, especially tactile allodynia after nerve injury.

本文言語英語
論文番号28
ジャーナルMolecular Pain
5
DOI
出版ステータス出版済み - 6 11 2009

All Science Journal Classification (ASJC) codes

  • 分子医療
  • 細胞および分子神経科学
  • 麻酔学および疼痛医療

フィンガープリント

「Behavioral phenotypes of mice lacking purinergic P2X<sub>4</sub> receptors in acute and chronic pain assays」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル