Alteration of cytokine profile following hemorrhagic shock

Cytokine. 2016 May:81:35-8. doi: 10.1016/j.cyto.2016.01.022. Epub 2016 Feb 5.

Abstract

Hemorrhage is one of the leading causes of death in patients with trauma. We recently demonstrated that resveratrol can improve cardiac function and prolong life following severe hemorrhagic injury (HI) in a rat model. The present work is focused on determining changes in NF-κB dependent gene expression in the heart and the systemic cytokine milieu following HI and the effect of resveratrol treatment. The results indicate an increase in phosphorylated NF-κB in the heart with a concomitant increase in the expression of NF-κB dependent genes following HI. There was also a significant increase of systemic cytokine levels, both pro and anti-inflammatory, following HI and resolution when treated with resveratrol. This study demonstrates the potential role NF-κB has in the physiological response to HI and the effectiveness of resveratrol in reducing immune activation.

Keywords: Hemorrhage; Inflammation; NFκB; Shock; Trauma.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Blotting, Western
  • Chemokine CCL3 / blood
  • Chemokine CCL3 / genetics
  • Chemokine CCL3 / metabolism
  • Cytokines / blood
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Gene Expression / drug effects
  • Interleukin-10 / blood
  • Interleukin-10 / genetics
  • Interleukin-10 / metabolism
  • Interleukin-2 / blood
  • Interleukin-2 / genetics
  • Interleukin-2 / metabolism
  • Interleukin-6 / blood
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Male
  • Myocardium / metabolism
  • Rats, Sprague-Dawley
  • Resveratrol
  • Reverse Transcriptase Polymerase Chain Reaction
  • Shock, Hemorrhagic / drug therapy*
  • Shock, Hemorrhagic / genetics
  • Shock, Hemorrhagic / metabolism*
  • Stilbenes / therapeutic use*
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Chemokine CCL3
  • Cytokines
  • Interleukin-2
  • Interleukin-6
  • Stilbenes
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Resveratrol