Aging exaggerates pulpal pain sensation by increasing the expression levels of nociceptive neuropeptides and inflammatory cytokines

Cytokine. 2023 Sep:169:156251. doi: 10.1016/j.cyto.2023.156251. Epub 2023 Jul 3.

Abstract

Background: Dental pain is a main clinical problem in the elderly population and its assessment and treatment make special challenges for health care services. However, the age-induced alteration in dental pain perception and the underlying molecular mechanism(s) has not yet been fully clarified.

Methods: Here, the effect of aging on nociceptive behaviors following inflammatory dental pulp pain was evaluated. Since prostaglandins, nociceptive neuropeptides, and inflammatory cytokines have critical roles in the development of aging as well as pain signaling, the expression levels of COX-2, CGRP, IL-1β, IL-6, TNF-α and its converting enzyme TACE were assessed in the trigeminal ganglion of young and aged rats with dental pain. Dental pulp pain was induced by intradental application of capsaicin (100 μg). The immunofluorescence (COX-2 and CGRP) and western blot techniques were used.

Results: The data showed that aged animals have different pattern of pain. So that, the mean of nociceptive scores was significantly greater in aged rats at 10 and 15 min after capsaicin injection. In aged rats, dental pain was persisting over 7 h, while it was disappeared at 300 min in young rats. Molecular data showed that dental pain significantly increased the expression of COX-2, CGRP, IL-1β, IL-6, TNF-α and TACE in the trigeminal ganglion of the young and aged rats. In addition, the amount of those parameters, except TACE, in capsaicin-treated aged animals were significantly (p < 0.05) greater than those in capsaicin-treated young rats.

Conclusion: It seems that the induction of pro-inflammatory cytokines in an acute inflammatory pulpal pain model may contribute, at least in part to the increased nociceptive behaviors and pain perception in aged rats.

Keywords: Aging; CGRP; COX-2; Capsaicin; Cytokines; Dental pain; Rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Animals
  • Calcitonin Gene-Related Peptide* / pharmacology
  • Capsaicin / pharmacology
  • Cyclooxygenase 2
  • Cytokines / pharmacology
  • Interleukin-6 / pharmacology
  • Neuropeptides*
  • Nociception
  • Pain
  • Rats
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Calcitonin Gene-Related Peptide
  • Capsaicin
  • Cyclooxygenase 2
  • Cytokines
  • Interleukin-6
  • Neuropeptides
  • Tumor Necrosis Factor-alpha