A Maternal Western-Style Diet Impairs Skeletal Muscle Lipid Metabolism in Adolescent Japanese Macaques

Author:

Greyslak Keenan T.1,Hetrick Byron1,Bergman Bryan C.2ORCID,Dean Tyler A.3,Wesolowski Stephanie R.4ORCID,Gannon Maureen5ORCID,Schenk Simon6,Sullivan Elinor L.789,Aagaard Kjersti M.10,Kievit Paul3ORCID,Chicco Adam J.11,Friedman Jacob E.12,McCurdy Carrie E.1ORCID

Affiliation:

1. 1Department of Human Physiology, University of Oregon, Eugene, OR

2. 2Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO

3. 3Division of Cardiometabolic Health, Oregon Health & Science University, Oregon National Primate Research Center, Beaverton, OR

4. 4Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO

5. 5Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN

6. 6Department of Orthopaedic Surgery, University of California, San Diego, La Jolla, CA

7. 7Division of Neuroscience, Oregon Health & Science University, Oregon National Primate Research Center, Beaverton, OR

8. 8Department of Psychiatry, Oregon Health & Science University, Portland, OR

9. 9Department of Behavioral Sciences, Oregon Health & Science University, Portland, OR

10. 10Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX

11. 11Department of Biomedical Sciences, Colorado State University, Fort Collins, CO

12. 12Harold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK

Abstract

Maternal consumption of a Western-style diet (mWD) during pregnancy alters fatty acid metabolism and reduces insulin sensitivity in fetal skeletal muscle. The long-term impact of these fetal adaptations and the pathways underlying disordered lipid metabolism are incompletely understood. Therefore, we tested whether a mWD chronically fed to lean, insulin-sensitive adult Japanese macaques throughout pregnancy and lactation would impact skeletal muscle oxidative capacity and lipid metabolism in adolescent offspring fed a postweaning (pw) Western-style diet (WD) or control diet (CD). Although body weight was not different, retroperitoneal fat mass and subscapular skinfold thickness were significantly higher in pwWD offspring consistent with elevated fasting insulin and glucose. Maximal complex I (CI)-dependent respiration in muscle was lower in mWD offspring in the presence of fatty acids, suggesting that mWD impacts muscle integration of lipid with nonlipid oxidation. Abundance of all five oxidative phosphorylation complexes and VDAC, but not ETF/ETFDH, were reduced with mWD, partially explaining the lower respiratory capacity with lipids. Muscle triglycerides increased with pwWD; however, the fold increase in lipid saturation, 1,2-diacylglycerides, and C18 ceramide compared between pwCD and pwWD was greatest in mWD offspring. Reductions in CI abundance and VDAC correlated with reduced markers of oxidative stress, suggesting that these reductions may be an early-life adaptation to mWD to mitigate excess reactive oxygen species. Altogether, mWD, independent of maternal obesity or insulin resistance, results in sustained metabolic reprogramming in offspring muscle despite a healthy diet intervention. Article Highlights In lean, active adolescent offspring, a postweaning Western-style diet (pwWD) leads to shifts in body fat distribution that are associated with poorer insulin sensitivity. Fatty acid–linked oxidative metabolism was reduced in skeletal muscles from offspring exposed to maternal Western-style diet (mWD) even when weaned to a healthy control diet for years. Reduced oxidative phosphorylation complex I–V and VDAC1 abundance partially explain decreased skeletal muscle respiration in mWD offspring. Prior exposure to mWD results in greater fold increase with pwWD in saturated lipids and bioactive lipid molecules (i.e. ceramide and sphingomyelin) associated with insulin resistance.

Funder

NIH

Eugene and Clarissa Evonuk Memorial Graduate Fellowship

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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