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High levels of portal TNF-alpha during abdominal aortic surgery in man

A Cabiè1, J C Farkas, C Fitting

  • 1Unité d'Immuno-Allergie, Institut Pasteur, Paris, France.

Cytokine
|September 1, 1993
PubMed

Insights

Gut ischemia during abdominal aortic surgery increases bacterial product lipopolysaccharide (LPS) and tumor necrosis factor-alpha (TNF-alpha) in portal and systemic circulation, suggesting a link to organ dysfunction.

Area of Science:

  • Gastroenterology
  • Surgical Physiology
  • Immunology

Background:

  • Gut ischemia during shock or multiple organ dysfunction syndrome may cause bacterial translocation, leading to increased cytokine production.
  • Lipopolysaccharide (LPS) translocation from the ischemic gut is a potential mechanism for elevated plasma cytokines.

Purpose of the Study:

  • To investigate the hypothesis that gut ischemia during abdominal aortic surgery leads to bacterial and/or LPS translocation.
  • To measure levels of LPS and cytokines in portal and systemic circulation during abdominal aortic surgery.

Main Methods:

  • Studied 14 patients undergoing abdominal aortic surgery with mild gut ischemia induced by bowel manipulation and aortic clamping.
  • Measured portal and systemic levels of LPS and cytokines (TNF-alpha, IL-6) before clamping and after reperfusion.
  • Compared measurements with a control group (n=7) undergoing internal carotid surgery.

Main Results:

  • Portal LPS was detected in 36% of patients after bowel manipulation and 71% after clamp release.
  • Similar portal and systemic LPS levels were observed after clamp release in aortic surgery patients.
  • Portal TNF-alpha levels were significantly higher than systemic levels post-manipulation and post-reperfusion (P=0.02, P=0.007).

Conclusions:

  • Bowel manipulation, aortic clamping, and reperfusion in abdominal aortic surgery result in comparable portal and systemic LPS levels.
  • Elevated portal TNF-alpha suggests local gut inflammatory response during aortic surgery.
  • Findings support the role of gut-derived LPS and cytokines in systemic inflammatory responses following major abdominal surgery.

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