Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells

In this study, the authors demonstrated that agents targeting skeletal muscle metabolism by modulating β2-adrenergic receptor-dependent signaling may prove beneficial as novel antidiabetic drugs.

Bibliographic Details
Main Authors: Jaroslawna Meister, Derek B. J. Bone, Jonas R. Knudsen, Luiz F. Barella, Thomas J. Velenosi, Dmitry Akhmedov, Regina J. Lee, Amanda H. Cohen, Oksana Gavrilova, Yinghong Cui, Gerard Karsenty, Min Chen, Lee S. Weinstein, Maximilian Kleinert, Rebecca Berdeaux, Thomas E. Jensen, Erik A. Richter, Jürgen Wess
Format: Article
Language:English
Published: Nature Portfolio 2022-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-27540-w
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author Jaroslawna Meister
Derek B. J. Bone
Jonas R. Knudsen
Luiz F. Barella
Thomas J. Velenosi
Dmitry Akhmedov
Regina J. Lee
Amanda H. Cohen
Oksana Gavrilova
Yinghong Cui
Gerard Karsenty
Min Chen
Lee S. Weinstein
Maximilian Kleinert
Rebecca Berdeaux
Thomas E. Jensen
Erik A. Richter
Jürgen Wess
author_facet Jaroslawna Meister
Derek B. J. Bone
Jonas R. Knudsen
Luiz F. Barella
Thomas J. Velenosi
Dmitry Akhmedov
Regina J. Lee
Amanda H. Cohen
Oksana Gavrilova
Yinghong Cui
Gerard Karsenty
Min Chen
Lee S. Weinstein
Maximilian Kleinert
Rebecca Berdeaux
Thomas E. Jensen
Erik A. Richter
Jürgen Wess
author_sort Jaroslawna Meister
collection DOAJ
description In this study, the authors demonstrated that agents targeting skeletal muscle metabolism by modulating β2-adrenergic receptor-dependent signaling may prove beneficial as novel antidiabetic drugs.
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spelling doaj.art-59a46724f573486ab78cf2fe37925d042022-12-22T04:09:17ZengNature PortfolioNature Communications2041-17232022-01-0113111410.1038/s41467-021-27540-wClenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cellsJaroslawna Meister0Derek B. J. Bone1Jonas R. Knudsen2Luiz F. Barella3Thomas J. Velenosi4Dmitry Akhmedov5Regina J. Lee6Amanda H. Cohen7Oksana Gavrilova8Yinghong Cui9Gerard Karsenty10Min Chen11Lee S. Weinstein12Maximilian Kleinert13Rebecca Berdeaux14Thomas E. Jensen15Erik A. Richter16Jürgen Wess17Molecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesDepartments of Nutrition, Exercise and Sports, University of CopenhagenMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesFaculty of Pharmaceutical Sciences, University of British ColumbiaDepartments of Integrative Biology and Pharmacology, Houston Medical SchoolMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesMouse Metabolism Core, National Institute of Diabetes and Digestive and Kidney DiseasesMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesDepartments of Genetics and Development, Vagelos College of Physicians and Surgeons, Columbia UniversityMetabolic Diseases Branch, National Institute of Diabetes and Digestive and Kidney DiseasesMetabolic Diseases Branch, National Institute of Diabetes and Digestive and Kidney DiseasesDepartments of Nutrition, Exercise and Sports, University of CopenhagenDepartments of Integrative Biology and Pharmacology, Houston Medical SchoolDepartments of Nutrition, Exercise and Sports, University of CopenhagenDepartments of Nutrition, Exercise and Sports, University of CopenhagenMolecular Signaling Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney DiseasesIn this study, the authors demonstrated that agents targeting skeletal muscle metabolism by modulating β2-adrenergic receptor-dependent signaling may prove beneficial as novel antidiabetic drugs.https://doi.org/10.1038/s41467-021-27540-w
spellingShingle Jaroslawna Meister
Derek B. J. Bone
Jonas R. Knudsen
Luiz F. Barella
Thomas J. Velenosi
Dmitry Akhmedov
Regina J. Lee
Amanda H. Cohen
Oksana Gavrilova
Yinghong Cui
Gerard Karsenty
Min Chen
Lee S. Weinstein
Maximilian Kleinert
Rebecca Berdeaux
Thomas E. Jensen
Erik A. Richter
Jürgen Wess
Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
Nature Communications
title Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
title_full Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
title_fullStr Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
title_full_unstemmed Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
title_short Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
title_sort clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
url https://doi.org/10.1038/s41467-021-27540-w
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