Organ-specific regulation of pro-inflammatory molecules in heart, lung, and kidney following brain death

J Surg Res. 2005 Jan;123(1):118-25. doi: 10.1016/j.jss.2004.07.245.

Abstract

Background: Nonspecific inflammatory events following brain death may increase the intensity of the immunological host response. The present study investigated the course of pro-inflammatory molecules in heart, lung, kidney, and plasma after brain death induction.

Materials and methods: Brain death was induced in five pigs by inflation of an intracranial Foley catheter and five pigs were sham-operated as controls. Each experiment was terminated 6 h after brain death/sham operation and the organs were harvested. We measured the mRNA and protein levels for TNF-alpha, IL-1beta, and IL-6 in heart, lung, kidney, and plasma. Additionally, the mRNA expression for IL-6R, ICAM-1, MCP-1, and TGF-beta was determined in each organ.

Results: After 6 h, the plasma cytokine levels were higher in the brain-dead animals than in the sham-operated. In heart, lung, and kidney there was an increase in IL-6 and IL-1beta following brain death, while TNF-alpha was up-regulated in lung only (P < 0.05). MCP-1 and TGF-beta were significantly higher in heart and lung and IL-6R increased in heart after brain death (P < 0.05).

Conclusions: Brain death was associated with non-uniform cytokine expression patterns in the investigated organs. These expression patterns may cause variable pro-inflammatory priming resulting in different degrees of damage and explain the organ-specific variation in outcomes after transplantations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Death / metabolism*
  • Cytokines / analysis
  • Cytokines / genetics*
  • Female
  • Gene Expression Profiling
  • Intercellular Adhesion Molecule-1 / genetics
  • Interleukin-1 / genetics
  • Interleukin-6 / genetics
  • Kidney / metabolism*
  • Lung / metabolism*
  • Male
  • Myocardium / metabolism*
  • Organ Specificity
  • RNA, Messenger / analysis
  • Receptors, Interleukin-6 / genetics
  • Swine
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Cytokines
  • Interleukin-1
  • Interleukin-6
  • RNA, Messenger
  • Receptors, Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1