Lower citrate synthase activity, mitochondrial complex expression, and fewer oxidative myofibers characterize skeletal muscle from growth-restricted fetal sheep

• Published in: American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2022-03, Vol.322 (3), p.R228-R240
• Main Authors: Stremming, Jane, Chang, Eileen I, Knaub, Leslie A, Armstrong, Michael L, Baker, 2nd, Peter R, Wesolowski, Stephanie R, Reisdorph, Nichole, Reusch, Jane E B, Brown, Laura D
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Biosynthesis; Citrate (si)-Synthase - metabolism; Citrate synthase; Female; Fetal Growth Retardation - metabolism; Fetus - metabolism; Fetuses; Gene expression; Gestation; Glycolysis; Hypoxia; Metabolism; Mitochondria; Mitochondria - metabolism; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - metabolism; Muscles; Musculoskeletal system; Nutrient deficiency; Oxidative metabolism; Oxidative Phosphorylation; Oxidative Stress - physiology; Phosphorylation; Placenta - metabolism; Placental Insufficiency - metabolism; Pregnancy; Respiration; Sheep; Skeletal muscle
• ISSN: 0363-6119; 1522-1490; 1522-1490
• DOI: 10.1152/ajpregu.00222.2021

Skeletal muscle from the late gestation sheep fetus with intrauterine growth restriction (IUGR) has evidence of reduced oxidative metabolism. Using a sheep model of placental insufficiency and IUGR, we tested the hypothesis that by late gestation, IUGR fetal skeletal muscle has reduced capacity for oxidative phosphorylation because of intrinsic deficits in mitochondrial respiration. We measured mitochondrial respiration in permeabilized muscle fibers from biceps femoris (BF) and soleus (SOL) from control and IUGR fetal sheep. Using muscles including BF, SOL, tibialis anterior (TA), and flexor digitorum superficialis (FDS), we measured citrate synthase (CS) activity, mitochondrial complex subunit abundance, fiber type distribution, and gene expression of regulators of mitochondrial biosynthesis. Ex vivo mitochondrial respiration was similar in control and IUGR muscle. However, CS activity was lower in IUGR BF and TA, indicating lower mitochondrial content, and protein expression of individual mitochondrial complex subunits was lower in IUGR TA and BF in a muscle-specific pattern. IUGR TA, BF, and FDS also had lower expression of type I oxidative fibers. Fiber-type shifts that support glycolytic instead of oxidative metabolism may be advantageous for the IUGR fetus in a hypoxic and nutrient-deficient environment, whereas these adaptions may be maladaptive in postnatal life.