Short-term pre- and post-operative stress prolongs incision-induced pain hypersensitivity without changing basal pain perception

Mol Pain. 2015 Dec 2:11:73. doi: 10.1186/s12990-015-0077-3.

Abstract

Background: Chronic stress has been reported to increase basal pain sensitivity and/or exacerbate existing persistent pain. However, most surgical patients have normal physiological and psychological health status such as normal pain perception before surgery although they do experience short-term stress during pre- and post-operative periods. Whether or not this short-term stress affects persistent postsurgical pain is unclear.

Results: In this study, we showed that pre- or post-surgical exposure to immobilization 6 h daily for three consecutive days did not change basal responses to mechanical, thermal, or cold stimuli or peak levels of incision-induced hypersensitivity to these stimuli; however, immobilization did prolong the duration of incision-induced hypersensitivity in both male and female rats. These phenomena were also observed in post-surgical exposure to forced swimming 25 min daily for 3 consecutive days. Short-term stress induced by immobilization was demonstrated by an elevation in the level of serum corticosterone, an increase in swim immobility, and a decrease in sucrose consumption. Blocking this short-term stress via intrathecal administration of a selective glucocorticoid receptor antagonist, RU38486, or bilateral adrenalectomy significantly attenuated the prolongation of incision-induced hypersensitivity to mechanical, thermal, and cold stimuli.

Conclusion: Our results indicate that short-term stress during the pre- or post-operative period delays postoperative pain recovery although it does not affect basal pain perception. Prevention of short-term stress may facilitate patients' recovery from postoperative pain.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corticosterone / blood
  • Female
  • Hormone Antagonists / pharmacology
  • Humans
  • Male
  • Mifepristone / pharmacology
  • Models, Animal
  • Pain Perception / physiology*
  • Pain Threshold / physiology*
  • Pain, Postoperative / physiopathology*
  • Rats
  • Rats, Sprague-Dawley
  • Restraint, Physical
  • Stress, Physiological*
  • Stress, Psychological*

Substances

  • Hormone Antagonists
  • Mifepristone
  • Corticosterone