Effect of capsaicin treatment on nociceptors in rat glabrous skin one day after plantar incision

Sinyoung Kang, Chaoran Wu, Ratan K. Banik, Timothy J. Brennan

Research output: Contribution to journalArticlepeer-review

35 Scopus citations


Dilute capsaicin produces a differential effect on incision-related pain behaviors depending upon the test; it reduces heat hyperalgesia and guarding pain but not mechanical hyperalgesia. This suggests that common mechanisms for heat hyperalgesia and guarding pain occur, and distinct mechanisms exist for mechanical hyperalgesia. The purpose of the present study was to evaluate the effect of capsaicin treatment on the activity of cutaneous nociceptors sensitized by incision to understand the mechanisms for the selective action of dilute capsaicin on incisional pain. We compared the effect of 0.05% capsaicin vs. vehicle treatment on pain behaviors after incision and on the activity of nociceptors from these same rats using the in vitro glabrous skin-nerve preparation. Immunohistochemical expression of protein gene product 9.5 (PGP9.5), neurofilament 200, calcitonin gene related peptide (CGRP) and isolectin B4 (IB4) in skin was also evaluated 1 week after 0.05% capsaicin infiltration. Infiltration of 0.05% capsaicin decreased CGRP and IB4/PGP9.5-immunoreactivity of nociceptors in skin. The same dose of capsaicin that inhibited heat hyperalgesia and guarding behavior interfered with chemo- and heat sensitivity of C-fibers. Neither mechanical hyperalgesia nor mechanosensitivity of nociceptors was affected by capsaicin, suggesting that the concentration of capsaicin used in this study did not cause fiber degeneration. These results demonstrate that nociceptors desensitized by capsaicin contribute to heat hyperalgesia and guarding pain after plantar incision. These putative TRPV1-expressing C-fibers are sensitized to heat and acid after incision, and the transduction of heat and chemical stimuli after plantar incision is impaired by dilute capsaicin.

Original languageEnglish (US)
Pages (from-to)128-140
Number of pages13
Issue number1
StatePublished - Jan 2010

Bibliographical note

Funding Information:
Support: This work was performed and in supported by the Department of Anesthesia at the University of Iowa and by National Institutes of Health , Bethesda, MD, Grants GM-55831 to T.J.B. Dr. Kang and Dr. Wu contributed equally to the manuscript.


  • Chemosensitive
  • Hyperalgesia
  • Pain
  • Postoperative
  • TRPV1


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