The Nonantibiotic Macrolide EM900 Attenuates House Dust Mite-Induced Airway Inflammation in a Mouse Model of Obesity-Associated Asthma.


Journal

International archives of allergy and immunology
ISSN: 1423-0097
Titre abrégé: Int Arch Allergy Immunol
Pays: Switzerland
ID NLM: 9211652

Informations de publication

Date de publication:
2020
Historique:
received: 20 04 2020
accepted: 15 05 2020
pubmed: 1 7 2020
medline: 2 2 2021
entrez: 30 6 2020
Statut: ppublish

Résumé

Obesity-associated asthma is characterized by type 2-low airway inflammation. We previously showed that EM900, which is a 12-membered nonantibiotic macrolide, suppressed airway inflammation in a mouse model of asthma exacerbation. The aim of this study was to clarify the effects of EM900 in obesity-associated asthma. BALB/c mice were fed a low-fat diet (LFD) or high-fat diet (HFD). Mice were intranasally sensitized and challenged with house dust mites (HDMs) and were orally administered EM900. Airway inflammation was assessed using inflammatory cells in bronchoalveolar lavage (BALF). Cytokines were examined by ELISA in lung tissues. Lung interstitial macrophages (CD45+, CD11clow, CD11b+, and Ly6c-) were counted by flow cytometry in single cells from lung tissues. Body weight increased significantly in the HFD compared with the LFD group. The total cell count and numbers of neutrophils and eosinophils in BALF were significantly suppressed by EM900 administration in the HFD-HDM group. The levels of interleukin (IL)-17A were increased in the HFD-HDM group compared with the LFD-HDM group, although the difference did not reach statistical significance. The levels of IL-17A, macrophage inflammatory protein 2, IL-1β, IL-5, and regulated on activation, normal T cell expressed and secreted in lung tissue were significantly suppressed by EM900 administration in the HFD-HDM group. The percentage of interstitial macrophages in lungs was significantly decreased by EM900 administration in the HFD-HDM group. Both type 2 and type 2-low airway inflammation were attenuated by EM900 in this obesity-associated asthma model. These results show that EM900 might be a candidate agent for the treatment of obesity-associated asthma.

Identifiants

pubmed: 32599580
pii: 000508709
doi: 10.1159/000508709
doi:

Substances chimiques

(8R,9S)-8,9-dihydro-6,9-epoxy-8,9-anhydropseudoerythromycin A 0
Anti-Asthmatic Agents 0
Antigens, Dermatophagoides 0
Interleukin-17 0
Erythromycin 63937KV33D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

665-674

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Hironori Sadamatsu (H)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Koichiro Takahashi (K)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan, takahak@cc.saga-u.ac.jp.

Hiroki Tashiro (H)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Yuki Kurihara (Y)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Go Kato (G)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Masaru Uchida (M)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Yoshihiko Noguchi (Y)

Ōmura Satoshi Memorial Institute, Kitasato University, Tokyo, Japan.

Keigo Kurata (K)

Institute of Tokyo Environmental Allergy, ITEA Inc, Tokyo, Japan.

Satoshi Ōmura (S)

Ōmura Satoshi Memorial Institute, Kitasato University, Tokyo, Japan.

Toshiaki Sunazuka (T)

Ōmura Satoshi Memorial Institute, Kitasato University, Tokyo, Japan.

Shinya Kimura (S)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Naoko Sueoka-Aragane (N)

Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

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Classifications MeSH