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Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity

Obese asthma is a unique phenotype of asthma characterized by non-allergic airway hyperresponsiveness (AHR) and inflammation which responds poorly to standard asthma therapy. Metformin is an oral hypoglycemic drug with insulin-sensitizing and anti-inflammatory properties. The objective of the curren...

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Autores principales: Gu, Chenjuan, Loube, Jeff, Lee, Rachel, Bevans-Fonti, Shannon, Wu, Tianshi David, Barmine, Jessica H., Jun, Jonathan C., McCormack, Meredith C., Hansel, Nadia N., Mitzner, Wayne, Polotsky, Vsevolod Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098833/
https://www.ncbi.nlm.nih.gov/pubmed/35574481
http://dx.doi.org/10.3389/fphys.2022.883275
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author Gu, Chenjuan
Loube, Jeff
Lee, Rachel
Bevans-Fonti, Shannon
Wu, Tianshi David
Barmine, Jessica H.
Jun, Jonathan C.
McCormack, Meredith C.
Hansel, Nadia N.
Mitzner, Wayne
Polotsky, Vsevolod Y.
author_facet Gu, Chenjuan
Loube, Jeff
Lee, Rachel
Bevans-Fonti, Shannon
Wu, Tianshi David
Barmine, Jessica H.
Jun, Jonathan C.
McCormack, Meredith C.
Hansel, Nadia N.
Mitzner, Wayne
Polotsky, Vsevolod Y.
author_sort Gu, Chenjuan
collection PubMed
description Obese asthma is a unique phenotype of asthma characterized by non-allergic airway hyperresponsiveness (AHR) and inflammation which responds poorly to standard asthma therapy. Metformin is an oral hypoglycemic drug with insulin-sensitizing and anti-inflammatory properties. The objective of the current study was to test the effect of metformin on AHR in a mouse model of diet-induced obesity (DIO). We fed 12-week-old C57BL/6J DIO mice with a high fat diet for 8 weeks and treated them with either placebo (control, n = 10) or metformin (n = 10) added in drinking water (300 mg/kg/day) during the last 2 weeks of the experiment. We assessed AHR, metabolic profiles, and inflammatory markers after treatments. Metformin did not affect body weight or fasting blood glucose, but significantly reduced serum insulin (p = 0.0117). Metformin reduced AHR at 30 mg/ml of methacholine challenge (p = 0.0052) without affecting baseline airway resistance. Metformin did not affect circulating white blood cell counts or lung cytokine mRNA expression, but modestly decreased circulating platelet count. We conclude that metformin alleviated AHR in DIO mice. This finding suggests metformin has the potential to become an adjuvant pharmacological therapy in obese asthma.
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spelling pubmed-90988332022-05-14 Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity Gu, Chenjuan Loube, Jeff Lee, Rachel Bevans-Fonti, Shannon Wu, Tianshi David Barmine, Jessica H. Jun, Jonathan C. McCormack, Meredith C. Hansel, Nadia N. Mitzner, Wayne Polotsky, Vsevolod Y. Front Physiol Physiology Obese asthma is a unique phenotype of asthma characterized by non-allergic airway hyperresponsiveness (AHR) and inflammation which responds poorly to standard asthma therapy. Metformin is an oral hypoglycemic drug with insulin-sensitizing and anti-inflammatory properties. The objective of the current study was to test the effect of metformin on AHR in a mouse model of diet-induced obesity (DIO). We fed 12-week-old C57BL/6J DIO mice with a high fat diet for 8 weeks and treated them with either placebo (control, n = 10) or metformin (n = 10) added in drinking water (300 mg/kg/day) during the last 2 weeks of the experiment. We assessed AHR, metabolic profiles, and inflammatory markers after treatments. Metformin did not affect body weight or fasting blood glucose, but significantly reduced serum insulin (p = 0.0117). Metformin reduced AHR at 30 mg/ml of methacholine challenge (p = 0.0052) without affecting baseline airway resistance. Metformin did not affect circulating white blood cell counts or lung cytokine mRNA expression, but modestly decreased circulating platelet count. We conclude that metformin alleviated AHR in DIO mice. This finding suggests metformin has the potential to become an adjuvant pharmacological therapy in obese asthma. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9098833/ /pubmed/35574481 http://dx.doi.org/10.3389/fphys.2022.883275 Text en Copyright © 2022 Gu, Loube, Lee, Bevans-Fonti, Wu, Barmine, Jun, McCormack, Hansel, Mitzner and Polotsky. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Gu, Chenjuan
Loube, Jeff
Lee, Rachel
Bevans-Fonti, Shannon
Wu, Tianshi David
Barmine, Jessica H.
Jun, Jonathan C.
McCormack, Meredith C.
Hansel, Nadia N.
Mitzner, Wayne
Polotsky, Vsevolod Y.
Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title_full Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title_fullStr Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title_full_unstemmed Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title_short Metformin Alleviates Airway Hyperresponsiveness in a Mouse Model of Diet-Induced Obesity
title_sort metformin alleviates airway hyperresponsiveness in a mouse model of diet-induced obesity
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098833/
https://www.ncbi.nlm.nih.gov/pubmed/35574481
http://dx.doi.org/10.3389/fphys.2022.883275
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