Short-term high-fat diet feeding protects from the development of experimental allergic asthma in mice.


Journal

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
ISSN: 1365-2222
Titre abrégé: Clin Exp Allergy
Pays: England
ID NLM: 8906443

Informations de publication

Date de publication:
09 2019
Historique:
received: 25 09 2018
revised: 11 06 2019
accepted: 17 06 2019
pubmed: 3 7 2019
medline: 12 9 2020
entrez: 3 7 2019
Statut: ppublish

Résumé

A close association between obesity and asthma has been described. The nature of this association remains elusive, especially with respect to allergic asthma. Controversial findings exist regarding the impact of short-term high-fat diet (HFD) feeding on the development of allergic asthma. To delineate the impact of short-term HFD feeding on the development of experimental allergic asthma. Female C57BL/6JRJ mice were fed with a short-term HFD or chow diet (CD) for 12 weeks. Allergic asthma was induced by intraperitoneal OVA/alum sensitization followed by repeated OVA airway challenges. We determined airway hyperresponsiveness (AHR) and pulmonary inflammation by histologic and flow cytometric analysis of immune cells. Furthermore, we assessed the impact of HFD on dendritic cell (DC)-mediated activation of T cells. Female mice showed a mild increase in body weight accompanied by mild metabolic alterations. Upon OVA challenge, CD-fed mice developed strong AHR and airway inflammation, which were markedly reduced in HFD-fed mice. Mucus production was similar in both treatment groups. OVA-induced increases in DC and CD4 These findings suggest that short-term HFD feeding attenuates the development of AHR, airway inflammation, pulmonary DC recruitment and MHC-II/CD40 expression leading to diminished Th1/17 but unchanged Th2 differentiation. Thus, short-term HFD feeding and associated metabolic alterations may have protective effects in allergic asthma development.

Sections du résumé

BACKGROUND
A close association between obesity and asthma has been described. The nature of this association remains elusive, especially with respect to allergic asthma. Controversial findings exist regarding the impact of short-term high-fat diet (HFD) feeding on the development of allergic asthma.
OBJECTIVE
To delineate the impact of short-term HFD feeding on the development of experimental allergic asthma.
METHODS
Female C57BL/6JRJ mice were fed with a short-term HFD or chow diet (CD) for 12 weeks. Allergic asthma was induced by intraperitoneal OVA/alum sensitization followed by repeated OVA airway challenges. We determined airway hyperresponsiveness (AHR) and pulmonary inflammation by histologic and flow cytometric analysis of immune cells. Furthermore, we assessed the impact of HFD on dendritic cell (DC)-mediated activation of T cells.
RESULTS
Female mice showed a mild increase in body weight accompanied by mild metabolic alterations. Upon OVA challenge, CD-fed mice developed strong AHR and airway inflammation, which were markedly reduced in HFD-fed mice. Mucus production was similar in both treatment groups. OVA-induced increases in DC and CD4
CONCLUSIONS/CLINICAL RELEVANCE
These findings suggest that short-term HFD feeding attenuates the development of AHR, airway inflammation, pulmonary DC recruitment and MHC-II/CD40 expression leading to diminished Th1/17 but unchanged Th2 differentiation. Thus, short-term HFD feeding and associated metabolic alterations may have protective effects in allergic asthma development.

Identifiants

pubmed: 31265181
doi: 10.1111/cea.13454
doi:

Substances chimiques

Dietary Fats 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1245-1257

Informations de copyright

© 2019 John Wiley & Sons Ltd.

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Auteurs

Torsten Schröder (T)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.
Institute of Nutritional Medicine, University Hospital Schleswig-Holstein, Lübeck, Germany.

Anna V Wiese (AV)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.

Fanny Ender (F)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.

Katharina M Quell (KM)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.

Tillman Vollbrandt (T)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.
Cell Analysis Core Facility, University of Lübeck, Lübeck, Germany.

Jannis Duhn (J)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.

Annika Sünderhauf (A)

Institute of Nutritional Medicine, University Hospital Schleswig-Holstein, Lübeck, Germany.

Axel Künstner (A)

The Lübeck Institute of Experimental Dermatology, Group of Medical Systems Biology, University of Lübeck, Lübeck, Germany.
Institute for Cardiogenetics, University of Lübeck, Lübeck, Germany.

Maria E Moreno-Fernandez (ME)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Stefanie Derer (S)

Institute of Nutritional Medicine, University Hospital Schleswig-Holstein, Lübeck, Germany.

Zouhair Aherrahrou (Z)

Institute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
DZHK (German Centre for Cardiovascular Research), University Heart Centre Lübeck, Lübeck, Germany.

Ian Lewkowich (I)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Senad Divanovic (S)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Christian Sina (C)

Institute of Nutritional Medicine, University Hospital Schleswig-Holstein, Lübeck, Germany.

Jörg Köhl (J)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Yves Laumonnier (Y)

Institute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.

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