Mono(2-ethylhexyl) phthalate induces both pro- and anti-inflammatory responses in rat alveolar macrophages through crosstalk between p38, the lipoxygenase pathway and PPARalpha

Inhal Toxicol. 2010 Feb;22(2):140-50. doi: 10.3109/08958370903019885.

Abstract

Airway inflammation is important in asthma pathogenesis. Recent epidemiological data have indicated an association between asthma symptoms in children and exposure to di(2-ethylhexyl) phthalate (DEHP). Thus, we have studied inflammatory responses in primary rat alveolar macrophages (AMs) after exposure to mono(2-ethylhexyl) phthalate (MEHP), the major primary metabolite of DEHP. First, we show that MEHP induces a dose-dependent release of the pro-inflammatory tumour necrosis factor-alpha (TNF-alpha) in AMs, giving a maximal (5-fold) increase at 0.7 mM. This concentration also induced some cell death. MEHP also induced phosphorylation of MAPK p38, while the p38 inhibitor SB 202190 reduced MEHP-induced TNF-alpha, suggesting a p38-dependent cytokine production. Next, we elucidated possible effects of MEHP on the 5-lipoxygenase (5-LO) pathway and found that MEHP caused increased leukotriene (LTB(4)) release. Further, we found that the 5-LO inhibitor nordihydrogualaretic acid (NDGA) significantly reduced both MEHP-induced TNF-alpha release and MEHP-induced formation of reactive oxygen species (ROS), supporting an involvement of the 5-LO pathway in MEHP induced inflammatory reactions. Last, we found that MK-886, a known inhibitor of peroxisome proliferator-activated receptor alpha (PPARalpha), increased the MEHP-induced TNF-alpha response. This indicates that MEPH-PPARalpha binding mediates an anti-inflammatory signal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents*
  • Cell Death / drug effects
  • Cell Membrane / drug effects
  • Cell Separation
  • Cyclooxygenase 2 / metabolism
  • Cytokines / biosynthesis
  • Diethylhexyl Phthalate / toxicity*
  • Inflammation / chemically induced*
  • Inflammation / pathology
  • Leukotrienes / biosynthesis
  • Lipoxygenase / physiology*
  • Macrophages, Alveolar / drug effects
  • Macrophages, Alveolar / pathology*
  • Male
  • PPAR alpha / drug effects
  • PPAR alpha / physiology*
  • Rats
  • Rats, Inbred WKY
  • Rats, Wistar
  • Reactive Oxygen Species
  • Receptor Cross-Talk / drug effects
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / metabolism
  • p38 Mitogen-Activated Protein Kinases / drug effects
  • p38 Mitogen-Activated Protein Kinases / physiology*

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Leukotrienes
  • PPAR alpha
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Diethylhexyl Phthalate
  • Lipoxygenase
  • Cyclooxygenase 2
  • p38 Mitogen-Activated Protein Kinases