歯髄鎮静と新しい歯髄鎮静薬作用点

• 北村 憲司

  福岡歯科大学 歯科薬理学

• 山崎 純

  福岡歯科大学 歯科薬理学

• 大久保 つや子

  福岡歯科大学 歯科薬理学

• 加藤 健一

  福岡歯科大学 歯科薬理学

• 内田 竜司

  福岡歯科大学口腔外科学

• 福泉 忠興

  福岡歯科大学 歯科薬理学

書誌事項

タイトル別名

• Dental sedation and new targets for the dental sedatives

抄録

Removal and sedation of hyperalgesia as well as treatment of tooth pain are the two of the major aim of dental treatments. With the use of a few compounds, such as eugenol or other phenol derivatives, hyperalgesia can be controlled. However, these compounds have an adverse effect for the dental pain control. Recent developments of molecular biology reveal new insights for the molecular mechanisms of nociception. In this review, we propose several possible targets for dental sedatives, such as bradykinin receptors, prostaglandin receptors, capsaicin receptors, ATP reeptors, voltage-dependent Na channels and voltage-dependent Ca channels. As activation of these receptors and ion channels promotes pain and inflammation, any block or inhibition of these targets would suppress the pain. Thus, the development of new drugs targeted to these sites may lead to the full control of the tooth pain.

収録刊行物

• 福岡歯科大学学会雑誌

  福岡歯科大学学会雑誌 26 (4), 209-217, 1999-12-31

  福岡歯科大学学会

キーワード

• Dental sedatives
• capsaicin receptor
• bradykinin receptor
• N-type
• Ca channel
• eugenol

詳細情報

• CRID: 1571135651969211136
• NII論文ID: 110004000868
• NII書誌ID: AN00216288
• ISSN: 03850064
• Web Site: https://search.jamas.or.jp/link/ui/2000172227
• 本文言語コード: ja
• データソース種別:
  • CiNii Articles