Decreased expression of peroxisome proliferator-activated receptor gamma in endotoxin-induced acute lung injury

Physiol Res. 2006;55(3):291-299. doi: 10.33549/physiolres.930822. Epub 2005 Aug 5.

Abstract

Peroxisome proliferator-activated receptor-gamma (PPAR- gamma), a member of the nuclear hormone receptor superfamily of ligand-activated transcription factors, possesses anti-inflammatory properties. The purpose of the present study was to investigate the profile of PPAR-gamma expression in the lung and to explore its functional significance in lipopolysaccharide (LPS)-induced acute lung injury. Thirty male Wistar rats were randomly assigned to one of the following five groups: saline control group and different LPS groups (2 h, 4 h, 6 h and 8 h after LPS 6 mg/kg i.v.). At predefined time points, blood samples were collected to measure plasma level of tumor necrosis factor (TNF)-alpha and lungs were removed to assay histopathological changes, wet-to-dry weight (W/D) ratio, myeloperoxidase (MPO) activity and TNF-alpha level. Expression of PPAR-gamma and activation of nuclear factor (NF)-kapaB p65 in lung tissues were also examined in each group. LPS injection resulted in marked lung damage and elevated levels of W/D ratio and MPO activity in the lung. Increased levels of TNF-alpha were also observed in the plasma and lung. These inflammatory events were associated with reduced expression of PPAR-gamma protein and with activation of NF-kapaB in the lung. Our data suggest that decreased expression of PPAR-gamma protein in lungs may contribute to the ongoing pulmonary inflammation and tissue injury in endotoxemia.

MeSH terms

  • Animals
  • Blotting, Western
  • Gene Expression / drug effects
  • Lipopolysaccharides / administration & dosage
  • Lipopolysaccharides / toxicity*
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / pathology
  • Male
  • PPAR gamma / genetics
  • PPAR gamma / metabolism*
  • Peroxidase / metabolism
  • Pulmonary Edema / genetics
  • Pulmonary Edema / metabolism
  • Pulmonary Edema / pathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Respiratory Distress Syndrome / chemically induced*
  • Respiratory Distress Syndrome / genetics
  • Respiratory Distress Syndrome / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factor RelA / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Lipopolysaccharides
  • PPAR gamma
  • RNA, Messenger
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • lipopolysaccharide, E coli O55-B5
  • Peroxidase