Open AccessInsulin Is Essential for the Recovery from Allodynia Induced by Complete Freund's Adjuvant
Author(s) -
Casey Gregory P.,
Paul Dennis,
Gould, III Harry J.
Publication year - 2010
Publication title -
pain medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.893
H-Index - 97
eISSN - 1526-4637
pISSN - 1526-2375
DOI - 10.1111/j.1526-4637.2010.00936.x
Subject(s) - medicine , subcutaneous injection , adjuvant , hyperalgesia , streptozotocin , freund's adjuvant , allodynia , diabetes mellitus , inflammation , anesthesia , pharmacology , nociception , endocrinology , receptor
Objective. To determine the effect of streptozotocin (STZ)‐induced diabetes on the development and recovery of thermal and mechanical hyperalgesia associated with inflammation induced by subcutaneous injection of complete Freund's adjuvant (CFA). Background. The response to nociceptive injury in diabetes differs from that seen in normal individuals in that diabetic patients have increased susceptibility to infections and recover slowly or incompletely from infections and tissue injury due to an abnormal inflammatory response. We have chosen to examine the effect of STZ‐induced hypoinsulinemia on the hyperalgesia associated with the enhanced inflammatory state that is induced by the subcutaneous injection of CFA to delineate the potential role of insulin in the development of chronic pain. Methods. STZ‐ and vehicle‐treated Sprague‐Dawley rats were tested using thermal and mechanical stimulation after subcutaneous injection of CFA. The behavioral response was compared with that similarly determined in non‐diabetic controls and insulin‐depleted rats that received insulin replacement. Results. Recovery of the thermal hyperalgesic response to baseline levels occurred over a period of 9–14 days, but the allodynic response to mechanical stimulation persisted for the duration of the study in STZ‐treated rats. Insulin replacement prevented the delay in recovery of mechanical allodynia, but had no obvious effect on nociception in uninflamed tissue. Conclusions. Normal insulin function is essential for recovery from mechanical allodynia associated with inflammation induced by CFA. Altered insulin metabolism may selectively influence fiber‐type specific mechanisms related to mechanical allodynia associated with inflammation and wound healing.