Phospholipases A2 and platelet-activating-factor acetylhydrolase in patients with acute respiratory distress syndrome

Crit Care Med. 2005 Apr;33(4):772-9. doi: 10.1097/01.ccm.0000158519.80090.74.

Abstract

Objective: Phospholipases A2 (PLA2) comprise a family of enzymes probably implicated in the development of acute respiratory distress syndrome (ARDS). The aim was to investigate PLA2 activities and characteristics in bronchoalveolar lavage (BAL) fluid, BAL cells, and plasma from patients with ARDS by a fluorometric method.

Design: Prospective, controlled study.

Setting: Fourteen-bed polyvalent intensive care unit in a university hospital.

Patients: A total of 31 mechanically ventilated patients, 20 with and 11 without ARDS, were studied.

Intervention: BAL was performed by fiberoptic bronchoscopy in mechanically ventilated patients with a controlled mechanical ventilation mode.

Measurements: PLA2 and platelet-activating-factor acetylhydrolase were determined in BAL fluid, cells, and plasma. For the classification of PLA2-specific inhibitors, Western blot analysis and their biochemical characteristics were used.

Results: In ARDS patients, increased PLA2 levels were detected in BAL fluid, BAL cells, and plasma compared with the control patients. PLA2 in BAL fluid was mainly type IIA secretory and cytosolic types. In plasma, type IIA secretory and cytosolic and a Ca-independent PLA2 were found. In BAL cells, a cytosolic form, probably a Ca-independent intracellular form, and a low activity of type IIA secretory PLA2 was also observed. Total PLA2 activity correlated inversely with Pao2/Fio2 ratio and positively with the mortality rate. Patients with direct ARDS exhibited higher PLA2 activity compared with patients with indirect ARDS. Platelet-activating-factor acetylhydrolase activity was higher in BAL fluid and plasma, but it was lower in BAL cells.

Conclusion: Ca-dependent, secretory, cytosolic, and Ca-independent forms of PLA2 and platelet-activating-factor acetylhydrolase could play important roles in the development or down-regulation of inflammation in ARDS, respectively.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / metabolism*
  • Acetylcholine / metabolism
  • Biomarkers / analysis
  • Blotting, Western
  • Bronchoalveolar Lavage Fluid / chemistry
  • Calcium / metabolism
  • Female
  • Humans
  • Logistic Models
  • Male
  • Middle Aged
  • Phospholipases A / metabolism*
  • Phospholipases A2
  • Respiratory Distress Syndrome / enzymology*
  • Survival Analysis

Substances

  • Biomarkers
  • Phospholipases A
  • Phospholipases A2
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Acetylcholine
  • Calcium