Journal of Endodontics
Volume 16, Issue 2 , Pages 78-84, February 1990

Effects of injury and inflammation on pulpal and periapical nerves*

  • Margaret R. Byers, PhD

      Affiliations

    • Corresponding Author InformationAddress requests for reprints to Dr. Byers, Department of Anesthesiology, RN-10, University of Washington, Seattle, WA 98195.
    • Dr. Byers is a research professor, Departments of Anesthesiology, Endodontics, and Biological Structure, University of Washington, Seattle, WA. Drs. Khayat, Kimberly, and Taylor are affiliated with the Department of Endodontics, University of Washington.
  • ,
  • Patrick E. Taylor, DDS, MSD

      Affiliations

    • Dr. Byers is a research professor, Departments of Anesthesiology, Endodontics, and Biological Structure, University of Washington, Seattle, WA. Drs. Khayat, Kimberly, and Taylor are affiliated with the Department of Endodontics, University of Washington.
  • ,
  • Bertrand G. Khayat, DDS, MSD

      Affiliations

    • Dr. Byers is a research professor, Departments of Anesthesiology, Endodontics, and Biological Structure, University of Washington, Seattle, WA. Drs. Khayat, Kimberly, and Taylor are affiliated with the Department of Endodontics, University of Washington.
  • ,
  • Charles L. Kimberly, DDS, MSD

      Affiliations

    • Dr. Byers is a research professor, Departments of Anesthesiology, Endodontics, and Biological Structure, University of Washington, Seattle, WA. Drs. Khayat, Kimberly, and Taylor are affiliated with the Department of Endodontics, University of Washington.

Several studies dealing with the reactions of dental nerve fibers to injury and inflammation are reviewed in this article. The subgroup of dental nerve fibers that contains calcitonin gene-related peptide (CGRP) was examined by immunocytochemistry at various times (1 to 35 days) after one of three degrees of injury: (a) Mild: Four day after making shallow cavities into cervical dentin of first molars of anesthetized adult rats, we found that CGRP fibers had sprouted into the subjacent odontoblast layer and dentin, and then returned to normal by 3 wk. (b) Intermediate: If the cervical cavities were acid etched, we found damage to the odontoblast layer, microabscess formation, and sprouting of CGRP fibers near the abscess, with subsequent formation of reparative dentin and healing. (c) Severe: If the pulp was exposed, a variety of reactions could occur, the most prevalent of which was a severe necrosis leading to development of periapical lesions. Analysis of the progressive stages of pulpal abscess and necrosis showed sprouting CGRP nerve fibers (a) at the retreating interface between abscess and vital pulp; (b) in periapical areas during onset of lesions; and (c) around chronic abscesses in granulomatous periodontal tissues. These studies are discussed in relation to various dental clinical problems such as hypersensitive teeth, episodic toothache, early onset of periapical lesions, dental anesthesia, and possible roles for sensory fibers and neuropeptides in tissue defense and healing.

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* This research was supported by NIH Grant DE 05159 to Dr. Byers and by NIH Grant 2-S07-RR05346 (BSRG) and the Graduate Endodontics Fund, University of Washington. Drs. C. L. Kimberly and P. E. Taylor received salary support from the U.S. Navy. Dr. B. G. Khayat received partial salary support from NIH Grant AG 00122.

PII: S0099-2399(06)81568-2

doi:10.1016/S0099-2399(06)81568-2

Journal of Endodontics
Volume 16, Issue 2 , Pages 78-84, February 1990