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Mechanism of analgesic action of some phenolic compounds used for dental practice.

Research Project

Project/Area Number 03670885
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Functional basic dentistry
Research InstitutionFukuoka Dental College

Principal Investigator

TAKAHASHI Hiroshi  Fukuoka Dental College, Department of Pharmacology, Professor., 歯学部, 教授 (00084260)

Co-Investigator(Kenkyū-buntansha) OHKUBO Tsuyako  Fukuoka Dental College, Department of Pharmacology, Assistant, 歯学部, 助手 (40099065)
SHIBATA Manabu  Fukuoka Dental College, Department of Pharmacology, Lecturer, 歯学部, 講師 (40099049)
Project Period (FY) 1991 – 1992
Project Status Completed (Fiscal Year 1992)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1992: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1991: ¥1,600,000 (Direct Cost: ¥1,600,000)
KeywordsPhenolic compounds / Eugenol / Guaiacol / Substance P release / Capsaicin / Nuerogenic inflammation / ユージノール / フェノ-ル性歯髄鎮痛薬 / 歯髄とサブスタンスP / ユ-ジノ-ル鎮痛 / グアヤコ-ル鎮痛 / カプサイシン鎮痛 / 歯髄炎
Research Abstract

Neurogenic inflammation, which involves the release of neuropeptides from capsaicin-sensitive sensory nerves, may contribute to inflammatory diseases in tissues such as skin, airways and gut. We had confirmed the existense of substance P (SP)- containing fibers in rat dental pulp, and have suggested that pulpitis may also be neurogenic inflammatory diseases. Capsaicin has been known as a releaser and depletor of SP, and phenolic compounds partly resemble capsaicin in chemical structure. Thus, the present study investigated the effects of eugenol (EG), guaiacol (GC) and thymol (TM) on analgesic action, blood flow and SP release in comparison with capsaicin, and the results were as follows : 1) Pain sensitivity was measured in three ways (heat, pressure and chemical stimuli), and the order of potency for analgesia was EG>HC>TM when these were administered intrathecally in mice, but was weaker than that of capsaicin. 2) EG increased cutaneous blood flow which was measured with a laser Doppler devise in rat hindpaw, and this was antagonized by spantide (an SP antagonist), in the same manner as capsaicin. 3) Rat mandibular incisor pulps were desected out and chopped, and slices weighing about 110 mg were transfered to superfusion chamber. SP release from slices of pulp was increased by EG and GC, but was less than by capsaicin. SP release from slices of rat spinal cord by EG and GC was equal to the potency of capsaicin.
These results suggest that phenol analogues such as EG and GC may have a neurotoxic action which releases and depletes SP from small diameter sensory fibers like capsaicin, and may cause analgesic and anti-inflammatory effect. Furthermore, it is possible that capsaicin will be able to use as analgesics for dental practice.

Report

(3 results)
  • 1992 Annual Research Report   Final Research Report Summary
  • 1991 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] 高橋宏,柴田学,大久保つや子: "ユ-ジノール、グアヤコールのアブスタンスPを中心にした消炎鎮痛作用機序" 歯科基礎医学会雑誌. (投稿準備中).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] H.Trowbride et al.: "Effect of zinc oxide-eugenol and hydroxide on intradental nerve activity." J.Endodontics. 8. 403 (1982)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] G.Kozam: "The effect of eugenol on nerve transmission." Oral Surg.44. 799 (1977)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] A.G.Hays et al.: "The effects of a series of capsaicin analoges on nociception and body temperature in the rat." Life Sci.34. 1241 (1984)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary

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Published: 1991-04-01   Modified: 2016-04-21  

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