Effect of PD98059, a selective MAPK3/MAPK1 inhibitor, on acute lung injury in mice

Int J Immunopathol Pharmacol. 2009 Oct-Dec;22(4):937-50. doi: 10.1177/039463200902200409.

Abstract

The aim of the present study is to evaluate the contribution of mitogen-activated protein kinase 1-3 MAPK3/MAPK1) in a model of acute lung inflammation in mice. Injection of carrageenan into the pleural cavity of mice elicited an acute inflammatory response characterized by: accumulation of fluid containing a large number of neutrophils (PMNs) in the pleural cavity, infiltration of PMNs in lung tissues and subsequent adhesion molecule expression (I-CAM and P-selectin), lipid peroxidation, and increased production of tumour necrosis factor-alpha, (TNF-alpha) and interleukin-1beta (IL-1beta). Furthermore, carrageenan induced lung apoptosis (Bax and Bcl-2 expression) as well as nitrotyrosine formation, NF-kB activation, and pJNK expression, as determined by immunohistochemical analysis of lung tissues and the degree of lung inflammation and tissue injury (histological score). Administration of PD98059, an inhibitor of MAPK3/MAPK1 (10 mg/kg) 1 h after carrageenan caused a reduction in all the parameters of inflammation measured. Thus, based on these findings we propose that inhibitors of the MAPK3/MAPK1 signaling pathways, such as PD98059, may be useful in the treatment of various inflammatory diseases.

MeSH terms

  • Acute Lung Injury / chemically induced
  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / enzymology
  • Acute Lung Injury / immunology
  • Acute Lung Injury / pathology
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Apoptosis / drug effects
  • Carrageenan
  • Cytokines / metabolism
  • Disease Models, Animal
  • Flavonoids / pharmacology*
  • I-kappa B Proteins / metabolism
  • Inflammation Mediators / metabolism
  • Intercellular Adhesion Molecule-1 / metabolism
  • Lipid Peroxidation / drug effects
  • Lung / drug effects*
  • Lung / enzymology
  • Lung / immunology
  • Lung / pathology
  • Male
  • Mice
  • Mitogen-Activated Protein Kinase 1 / antagonists & inhibitors*
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / antagonists & inhibitors*
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • NF-KappaB Inhibitor alpha
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • P-Selectin / metabolism
  • Phosphorylation
  • Pleurisy / chemically induced
  • Pleurisy / drug therapy*
  • Pleurisy / enzymology
  • Pleurisy / immunology
  • Pleurisy / pathology
  • Protein Kinase Inhibitors / pharmacology*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / drug effects
  • Transcription Factor RelA / metabolism
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism
  • bcl-2-Associated X Protein / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Anti-Inflammatory Agents
  • Bax protein, mouse
  • Cytokines
  • Flavonoids
  • I-kappa B Proteins
  • Inflammation Mediators
  • Nfkbia protein, mouse
  • P-Selectin
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Rela protein, mouse
  • Transcription Factor RelA
  • bcl-2-Associated X Protein
  • Intercellular Adhesion Molecule-1
  • NF-KappaB Inhibitor alpha
  • Nitric Oxide
  • 3-nitrotyrosine
  • Tyrosine
  • Carrageenan
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Mapk1 protein, mouse
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • p38 Mitogen-Activated Protein Kinases
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one