Suppression of allergen-induced airway inflammation and immune response by the peroxisome proliferator-activated receptor-alpha agonist fenofibrate

被引:26
作者
Delayre-Orthez, Carine [1 ]
Becker, Julien [1 ]
Auwerx, Johan [2 ,3 ]
Frossard, Nelly [1 ]
Pons, Francoise [1 ]
机构
[1] Univ Louis Pasteur Strasbourg 1, Fac Pharm, Inflammat & Environm Asthme EA3771, F-67401 Illkirch Graffenstaden, France
[2] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France
[3] Inst Clin Souris, Illkirch Graffenstaden, France
关键词
fenofibrate; PPAR alpha; inflammation; allergy; asthma;
D O I
10.1016/j.ejphar.2007.11.040
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study, we have assessed the effect of the peroxisome proliferator-activated receptor-alpha (PPAR alpha) agonist fenofibrate on allergen-induced airway inflammation and immune response. C57BL/6 or PPAR alpha knock-out (PPAR alpha(-/-)) mice were sensitized with ovalbumin and challenged with ovalbumin alone or with ovalbumin+lipopolysaccharides. Fenofibrate was administered to allergen-exposed animals during challenge only or from the day prior to sensitization to the end of challenge. Inflammation and immune response were assessed by determining cell counts and cytokine levels in bronchoalveolar lavage fluids, expression of the transcription factors Gata-3 and T-bet in lung tissue and ovalbuminspecific IgE and IgG2a in serum. Treatment with fenofibrate (0.15-15 mg/day) during allergen challenge dose-dependently reduced airway inflammatory cell infiltrate induced by ovalbumin in C57BL/6 mice. Reduction reached 74.3% (P<0.001) in animals treated with 15 mg/day of the PPAR alpha agonist, whereas this treatment failed to suppress cell infiltrate induced by allergen in PPAR alpha(-/-) mice. In addition, when administered from the day prior to sensitization to the end of challenge, fenofibrate (15 mg/day) triggered switching of the immune response to allergen towards a Th1 profile, as evidenced by an increase in IgG2a levels, a reduction in IL(interleukin)-4 and IL-5 together with an increase in interferon-gamma, and a decrease in Gata-3/T-bet expression ratio. Upon challenge with ovalbumin+lipopolysaccharides, sensitized mice developed a severe inflammatory response characterized by infiltration of eosinophils, neutrophils, lymphocytes and macrophages and by increased release of IL-4, IL-5, tumor necrosis factor-alpha, macrophage-inflammatory protein-2 and monocyte chemoattractant protein-1. Administration of fenofibrate during allergen challenge dramatically reduced all responses. In conclusion, our data clearly demonstrate that fenofibrate exhibits an anti-inflammatory activity in allergic asthma, including in severe conditions, and that the PPAR alpha agonist is also capable of switching the immune response to allergen towards a Th1 profile when given from the day prior to sensitization. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 27 条
[1]   Corticosteroids: The drugs to beat [J].
Barnes, PJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 533 (1-3) :2-14
[2]   Pathophysiology of asthma [J].
Barnes, PJ .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 42 (01) :3-10
[3]  
Barnes PJ, 1998, PHARMACOL REV, V50, P515
[4]   NF-kappa B: A pivotal role in asthma and a new target for therapy [J].
Barnes, PJ ;
Adcock, IM .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (02) :46-50
[5]   Regulation of inflammation by PPARs: a future approach to treat lung inflammatory diseases? [J].
Becker, Julien ;
Delayre-Orthez, Carine ;
Frossard, Nelly ;
Pons, Francoise .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2006, 20 (05) :429-447
[6]   New anti-inflammatory therapies and targets for asthma and chronic obstructive pulmonary disease [J].
Belvisi, MG ;
Hele, DJ ;
Birrell, MA .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2004, 8 (04) :265-285
[7]   Activation of proliferator-activated receptors α and γ induces apoptosis of human monocyte-derived macrophages [J].
Chinetti, G ;
Griglio, S ;
Antonucci, M ;
Torra, IP ;
Delerive, P ;
Majd, Z ;
Fruchart, JC ;
Chapman, J ;
Najib, J ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25573-25580
[8]   Comparing protocols for preparation of DNA-free total yeast RNA suitable for RT-PCR [J].
Del Aguila, EM ;
Dutra, MB ;
Silva, JT ;
Paschoalin, VMF .
BMC MOLECULAR BIOLOGY, 2005, 6
[9]   Dose-dependent effects of endotoxins on allergen sensitization and challenge in the mouse [J].
Delayre-Orthez, C ;
de Blay, F ;
Frossard, N ;
Pons, F .
CLINICAL AND EXPERIMENTAL ALLERGY, 2004, 34 (11) :1789-1795
[10]   Peroxisome proliferator-activated receptor α negatively regulates the vascular inflammatory gene response by negative cross-talk with transcription factors NF-κB and AP-1 [J].
Delerive, P ;
De Bosscher, K ;
Besnard, S ;
Vanden Berghe, W ;
Peters, JM ;
Gonzalez, FJ ;
Fruchart, JC ;
Tedgui, A ;
Haegeman, G ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32048-32054