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High fat diet induces airway remodeling in ApoE deficient mice: An association with an increase in circulatory and airway inflammatory factors
Author(s) -
Naura Amarjit Singh,
Hans Chetan,
Zerfaoui Mourad,
Errami Youssef,
Ju Jihang,
Kim Hogyoung,
Matrougui Khalid,
Boulares Hamid A
Publication year - 2009
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.23.1_supplement.572.3
Subject(s) - inflammation , tumor necrosis factor alpha , medicine , cytokine , endocrinology , lung , airway , immunology , surgery
Objective To examine the effect of high fat (HF) diet and associated hypercholesterolemia on airway integrity in mice. Methods The HF diet‐induced hypercholesterolemia and atherogenesis mouse (ApoE −/− ) model was used to conduct the study. Results HF diet induced systemic production of inflammatory cytokines including TNF‐α, IFN‐γ, GMC‐SF, RANTES, IL‐1α, IL‐2, and IL‐12 in ApoE− /− mice with TNFα as the predominant cytokine. Concomitantly, TNF‐α, IFN‐γ, and MIP‐1α were detected in brochoalveolar lavage fluids of these mice, coinciding with airway inflammation consisting primarily of monocytes/macrophages. Such airway inflammation was associated with marked collagen deposition, an increase in MMP‐9 activity and TGF‐β distribution in lungs of HF‐fed ApoE− /− mice. Direct intratracheal TNFα‐administration induced an inflammation pattern in wild type mice similar to that observed in HF diet‐fed ApoE− /− mice suggesting that TNFα may be an important player in hypercholesterolemia‐induced airway inflammation. Indeed, TNFα administration induced expression of MCP‐1, IL‐1β, TGFα1, adhesion molecules, collagen 1 and TNFα itself in the lungs of treated mice, all of which are known to be important for airway remodeling. Conclusion These results suggest that a HF diet and associated hypercholesterolemia may promote chronic inflammatory conditions in lungs that are conducive to airway remodeling.