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The peroxisome proliferator‐activated receptor alpha agonist fenofibrate decreases airway reactivity to methacholine and increases endothelial nitric oxide synthase phosphorylation in mouse lung
Author(s) -
Becker Julien,
DelayreOrthez Carine,
Frossard Nelly,
Pons Françoise
Publication year - 2012
Publication title -
fundamental and clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.655
H-Index - 73
eISSN - 1472-8206
pISSN - 0767-3981
DOI - 10.1111/j.1472-8206.2011.00935.x
Subject(s) - fenofibrate , methacholine , enos , endocrinology , medicine , chemistry , agonist , peroxisome proliferator activated receptor , endothelial nos , nitric oxide , nitric oxide synthase , receptor , lung , pharmacology , respiratory disease
In the present study, we have investigated the effect of the peroxisome proliferator‐activated receptor α (PPARα) agonist fenofibrate on airway reactivity and the role of the endothelial nitric oxide synthase (eNOS)/NO pathway in this effect. Airway reactivity to methacholine was assessed in C57BL/6 mice treated or not with fenofibrate by whole‐body plethysmography. In some experiments, animals were administered with the NOS inhibitor L‐NAME, one hour before airway reactivity measurement. Expression and phosphorylation of eNOS were evaluated in lung homogenates from fenofibrate and control animals using Western blotting. Fenofibrate dose and time dependently decreased airway reactivity to methacholine in mice. A statistically significant ( P < 0.05) reduction was observed after a treatment of 10 days with a dose of 3 or 15 mg/day fenofibrate. Mice treated with fenofibrate and administered with l ‐NAME exhibited similar reactivity to methacholine than vehicle‐treated mice administered with the NOS inhibitor, suggesting that NO mediates fenofibrate‐induced decrease in airway reactivity. eNOS levels remained unchanged in the lung from mice treated with fenofibrate, but phosphorylation of the enzyme at Ser‐1177 was increased by 118% ( P < 0.05). Taken together, our data demonstrate that fenofibrate downregulates airway reactivity to methacholine in the mouse and suggest that this effect could involve an increase in NO generation through an enhanced eNOS phosphorylation.