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Oxygen radical generation by emigrated, intra-abdominal, and circulating PMNLs during human secondary peritonitis

K Holzer1, A Richter, D Henrich

  • 1Department of General Surgery, Johann Wolfgang Goethe University, Frankfurt, Germany.

Shock (Augusta, Ga.)
|February 28, 2001
PubMed

Insights

Polymorphonuclear leukocytes (PMNLs) show varied oxygen radical generation during peritonitis. Emigrated PMNLs produced more radicals in low severity cases, while circulating PMNLs increased radical production in severe peritonitis.

Area of Science:

  • Immunology
  • Cellular Biology
  • Biochemistry

Background:

  • Peritonitis is an inflammatory condition with significant morbidity and mortality.
  • Polymorphonuclear leukocytes (PMNLs) play a crucial role in the inflammatory response.
  • Oxygen radical generation by PMNLs is implicated in tissue damage during inflammation.

Purpose of the Study:

  • To characterize oxygen radical generation by emigrated (ePMNLs) and circulating (cPMNLs) PMNLs during peritonitis.
  • To compare oxygen radical production between patients with low (MPI < 26) and high (MPI ≥ 26) Mannheim Peritonitis Index (MPI).

Main Methods:

  • Lucigenin-enhanced chemiluminescence was used to measure spontaneous and stimulated oxygen radical generation.
  • Oxygen radical production was assessed in ePMNLs and cPMNLs from patients with varying peritonitis severity.
  • Stimulants included FMLP, PMA, and A23 187.

Main Results:

  • In low MPI patients (group 1), ePMNLs showed significantly higher spontaneous and stimulated oxygen radical generation than cPMNLs.
  • In high MPI patients (group 2), cPMNLs exhibited a marked increase in oxygen radical generation within 48 hours post-diagnosis and surgery, unlike ePMNLs.
  • A23 187-stimulated radical generation was significantly higher in cPMNLs compared to ePMNLs in group 2.

Conclusions:

  • PMNLs display significant functional heterogeneity in oxygen radical generation during secondary peritonitis.
  • Severe peritonitis (MPI ≥ 26) is associated with increased oxygen radical production by cPMNLs, but not ePMNLs.

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