17α-Estradiol alleviates high-fat diet-induced inflammatory and metabolic dysfunction in skeletal muscle of male and female mice

Author:

Bubak Matthew P.1ORCID,Mann Shivani N.2,Borowik Agnieszka K.1ORCID,Pranay Atul1,Batushansky Albert13,Vieira de Sousa Neto Ivo1ORCID,Mondal Samim A.1ORCID,Doidge Stephen M.1,Davidyan Arik4ORCID,Szczygiel Marcelina M.1,Peelor Frederick F.1,Rigsby Sandra1,Broomfield Matle E.1,Lacy Charles I.5,Rice Heather C.5,Stout Michael B.16ORCID,Miller Benjamin F.16ORCID

Affiliation:

1. Aging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States

2. Department of Neuroscience, University of Arizona, Tucson, Arizona, United States

3. Ilse Katz Institute for Nanoscale Science & Technology, Ben-Gurion University of the Negev, Beer-Sheba, Israel

4. Department of Biological Sciences, California State University, Sacramento, California, United States

5. Department of Biochemistry and Molecular Biology, Oklahoma Center for Geroscience and Healthy Brain Aging, Oklahoma City, Oklahoma, United States

6. Oklahoma City Veterans Affairs Medical Center, Oklahoma City, Oklahoma, United States

Abstract

Using a multiomics approach, we show that 17α-E2 alleviates HFD-induced metabolic detriments in skeletal muscle by altering bioactive lipid intermediates, inflammatory cytokines, and the abundance of proteins related to lipolysis and muscle contraction. The positive effects of 17α-E2 in skeletal muscle occur in both sexes but differ in their outcome.

Funder

U.S. Department of Veterans Affairs

Sao Paulo Research Foundation

HHS | National Institutes of Health

Publisher

American Physiological Society

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