Mu opioid signaling protects against acute murine intestinal injury in a manner involving Stat3 signaling.

Abstract

Opiates have long been used as analgesics to relieve pain associated with various medical conditions. Here, we evaluated the effect and mechanism of mu opioid signaling on the intestinal wound healing response and assessed downstream pathways known to be protective against intestinal injury. Mice (C57BL/6) were exposed to 3% dextran sodium sulfate (DSS) for 7 days or 4% DSS for 5 days followed by 7 days of water. The mu opioid receptor (MOR)-specific agonist [D-Arg2,Lys4]dermorphin-(1,4)-amide (DALDA) and the antagonist cyprodime were injected s.c. daily for in vivo studies or used for in vitro analysis. We found that MOR activation attenuated DSS-induced histologic and gross intestinal injury and weight loss; diminished Ifng, Tnf, and Il6 mRNA expression; and promoted intestinal healing during recovery. DALDA also enhanced colonocyte proliferation (Ki-67 staining) by 350%. MOR activation increased Stat3 phosphorylation in both DALDA-treated mice and the CMT-93 cell line. Importantly, DALDA-induced colonocyte migration was completely ablated by shStat3 knockdown. Together, this work shows that MOR activation protects against and enhances recovery from DSS-induced intestinal injury. This is associated with an increase in Stat3 activation. Furthermore, Stat3 is required for DALDA-induced colonocyte migration. Consequently, manipulation of MOR signaling may represent a novel means to promote mucosal healing and to maintain intestinal homeostasis after intestinal injury.

• Authors: Jason R Goldsmith, Joshua M Uronis, Christian Jobin
• Journal: The American journal of pathology (Am J Pathol) Vol. 179 Issue 2 Pg. 673-83 (Aug 2011) ISSN: 1525-2191 [Electronic] United States
• PMID: 21801866 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
• Copyright: Copyright © 2011 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

Chemical References

• Ki-67 Antigen
• NF-kappa B
• Oligopeptides
• Receptors, Opioid, mu
• STAT3 Transcription Factor
• tyrosyl-arginyl-phenylalanyl-lysinamide
• Dextran Sulfate

Topics

• Animals
• Cell Proliferation
• Colon (cytology)
• Dextran Sulfate (pharmacology)
• Homeostasis
• Intestines (injuries)
• Ki-67 Antigen (biosynthesis)
• Mice
• Mice, Inbred C57BL
• Mice, Transgenic
• NF-kappa B (genetics)
• Oligopeptides (pharmacology)
• Receptors, Opioid, mu (metabolism)
• STAT3 Transcription Factor (metabolism)
• Signal Transduction
• Time Factors