• DocumentCode
    3103784
  • Title

    Molecular Mechanism of Neuropathic Pain

  • Author

    Sawada, Yosuke ; Hosokawa, Hiroshi ; Matsumura, Kiyoshi ; Kobayashi, Shigeo

  • Author_Institution
    Kyoto Univ., Kyoto
  • fYear
    2008
  • fDate
    17-17 Jan. 2008
  • Firstpage
    173
  • Lastpage
    176
  • Abstract
    There are many patients suffering from neuropathic pain. Reactive oxygen species (ROS) is thought to be a mediator of neuropathic pain. In addition, neuropatic pain is aggravated by low temperature. However, receptor of ROS and low temperature is unknown. TRPA1 is activated by pain- producing agents such as allyl isothiocyanate or formaldehyde. We hypothesized that TRPA1 is receptor of ROS and low temperature on nociceptor. The purpose of present study is to investigate the validity of this hypothesis using Ca2+ imagining, patch clamp. Deep cooling (<17degC) and ROS activates TRPA1 expressing HEK293 cells. These results indicate that TRPA1 is receptor of ROS and low temperature.
  • Keywords
    biology computing; neurophysiology; Ca2+ imaging; HEK293 cells; ROS receptors; TRPA1; molecular mechanism; neuropathic pain; nociceptor; patch clamp; reactive oxygen species; Clamps; Cooling; Educational technology; Fluorescence; Glass; Informatics; Mice; Neurons; Neuropathic pain; Temperature; TRPA1; pain;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Informatics Education and Research for Knowledge-Circulating Society, 2008. ICKS 2008. International Conference on
  • Conference_Location
    Kyoto
  • Print_ISBN
    978-0-7695-3128-1
  • Type

    conf

  • DOI
    10.1109/ICKS.2008.24
  • Filename
    4460488