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Maternal obesity reduces oxidative capacity in fetal skeletal muscle of Japanese macaques
Carrie E. McCurdy, Simon Schenk, Byron Hetrick, Julie Houck, Brian G. Drew, Spencer Kaye, Melanie Lashbrook, Bryan C. Bergman, Diana L. Takahashi, Tyler A. Dean, Travis Nemkov, Ilya Gertsman, Kirk C. Hansen, Andrew Philp, Andrea L. Hevener, Adam J. Chicco, Kjersti M. Aagaard, Kevin L. Grove, Jacob E. Friedman
Carrie E. McCurdy, Simon Schenk, Byron Hetrick, Julie Houck, Brian G. Drew, Spencer Kaye, Melanie Lashbrook, Bryan C. Bergman, Diana L. Takahashi, Tyler A. Dean, Travis Nemkov, Ilya Gertsman, Kirk C. Hansen, Andrew Philp, Andrea L. Hevener, Adam J. Chicco, Kjersti M. Aagaard, Kevin L. Grove, Jacob E. Friedman
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Research Article Metabolism Muscle biology

Maternal obesity reduces oxidative capacity in fetal skeletal muscle of Japanese macaques

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Abstract

Maternal obesity is proposed to alter the programming of metabolic systems in the offspring, increasing the risk for developing metabolic diseases; however, the cellular mechanisms remain poorly understood. Here, we used a nonhuman primate model to examine the impact of a maternal Western-style diet (WSD) alone, or in combination with obesity (Ob/WSD), on fetal skeletal muscle metabolism studied in the early third trimester. We find that fetal muscle responds to Ob/WSD by upregulating fatty acid metabolism, mitochondrial complex activity, and metabolic switches (CPT-1, PDK4) that promote lipid utilization over glucose oxidation. Ob/WSD fetuses also had reduced mitochondrial content, diminished oxidative capacity, and lower mitochondrial efficiency in muscle. The decrease in oxidative capacity and glucose metabolism was persistent in primary myotubes from Ob/WSD fetuses despite no additional lipid-induced stress. Switching obese mothers to a healthy diet prior to pregnancy did not improve fetal muscle mitochondrial function. Lastly, while maternal WSD alone led only to intermediary changes in fetal muscle metabolism, it was sufficient to increase oxidative damage and cellular stress. Our findings suggest that maternal obesity or WSD, alone or in combination, leads to programmed decreases in oxidative metabolism in offspring muscle. These alterations may have important implications for future health.

Authors

Carrie E. McCurdy, Simon Schenk, Byron Hetrick, Julie Houck, Brian G. Drew, Spencer Kaye, Melanie Lashbrook, Bryan C. Bergman, Diana L. Takahashi, Tyler A. Dean, Travis Nemkov, Ilya Gertsman, Kirk C. Hansen, Andrew Philp, Andrea L. Hevener, Adam J. Chicco, Kjersti M. Aagaard, Kevin L. Grove, Jacob E. Friedman

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Figure 5

Reverting obese females to a healthy diet prior to pregnancy does not restore oxidative capacity in fetal gastrocnemius.

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Reverting obese females to a healthy diet prior to pregnancy does not re...
(A) Respiratory flux (JO2) adjusted according to muscle weight was measured after sequential addition of pyruvate/malate (P/M), ADP, glutamate (G), succinate (S), oligomycin (OMY) and the uncoupling agent carbonylcyanide p-trifluoromethoxy-phenylhydrazone (U) in permeabilized muscle fiber bundles (PMFBs) from male (circles) and female (triangles) fetal offspring of lean/overweight dams (n = 7) that had only received control diet (Ln/CTR), obese dams chronically fed a Western-style diet (Ob/WSD, n = 9), and obese dams chronically (≤ 9 years) fed a WSD before pregnancy but reverted to CTR diet prior to pregnancy (Ob/CTR, n = 5). (B) JO2 was measured after sequential addition of palmitoylcarnitine and malate (FA), ADP, pyruvate (FA+P), G, S, U, and the complex I inhibitor rotenone (Rot) in PMFBs from Ln/CTR (n = 5), Ob/WSD (n = 8) and Ob/CTR (n = 4). (C) Electron transfer system (ETS) coupling efficiency was calculated as 1 – (CI + IIL) divided by the subsequent noncoupled ETS capacity during the pyruvate protocol. (D) Coupling control ratio was calculated as leak respiration in the presence of OMY (CI + IIL) divided by the preceding uninhibited oxidative phosphorylation flux (CI+IIP) during the pyruvate protocol. (E) Citrate synthase (CS) activity was measured in frozen tissues corresponding to the respirometry samples. Data were analyzed by 2-way ANOVA (maternal group × substrate) with Tukey post-hoc in A and B or 1-way ANOVA in C–E. Letters are used to indicate significant post-hoc differences (P < 0.05) between maternal groups. Groups with the same letter are not significantly different from each other. Individual data points and the group mean + SEM are shown.

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