Increased Skeletal Muscle Fiber Cross-Sectional Area, Muscle Phenotype Shift, and Altered Insulin Signaling in Rat Hindlimb Muscles in a Prenatally Androgenized Rat Model for Polycystic Ovary Syndrome

Int J Mol Sci. 2020 Oct 25;21(21):7918. doi: 10.3390/ijms21217918.

Abstract

Women with polycystic ovary syndrome (PCOS) are reported to have greater lean mass and insulin resistance. To examine muscular changes in a prenatally androgenized (PNA) rat model for PCOS, Sprague-Dawley rats were exposed to 5 mg testosterone or vehicle daily on gestational days 16-19. At 15 weeks of age, endurance on a rota-rod treadmill was measured. At 16 weeks of age, fasting blood glucose and insulin, hindlimb skeletal muscle mass, muscle fiber cross-sectional area (CSA) and composition, and intra- and peri-muscular lipid droplets were examined. Expression of mitochondrial marker ATP synthase and insulin signaling proteins were also investigated. Compared with controls, PNA female rats demonstrated greater total body and hindlimb muscle weights, greater muscle fiber CSA, and trending reduced time on the rota-rod. An increase in fibers co-expressing the slow and fast isoforms of myosin (90 vs. 86%, p < 0.05) and greater expression of ATP synthase (6-fold, p < 0.005) were observed in the gastrocnemius (GN) muscle. More lipid content was observed in GN and tibialis anterior (TA) muscles. PNA rats had elevated fasting serum insulin (1.9 vs. 1.2 ng/mL, p < 0.005) but comparable fasting glucose. Expression of total and Ser636/9-phosphorylated IRS1 were altered in PNA rat hindlimb muscles. Together, skeletal muscle alterations in hindlimb muscles of a PNA rat model for PCOS may represent consequences of, or adaptations to, insulin resistance in this model.

Keywords: IRS1; PCOS; hyperandrogenemia; insulin resistance; insulin signaling; intra-muscular lipids; muscle cross-sectional area; muscle fiber type; peri-muscular lipids.

MeSH terms

  • Animals
  • Body Weight / physiology
  • Disease Models, Animal
  • Female
  • Hindlimb / metabolism
  • Hindlimb / physiopathology*
  • Humans
  • Insulin Resistance / physiology*
  • Lipids / analysis
  • Motor Activity / physiology
  • Muscle Fibers, Skeletal / metabolism
  • Muscle Fibers, Skeletal / physiology*
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / physiopathology*
  • Phenotype
  • Polycystic Ovary Syndrome / chemically induced
  • Polycystic Ovary Syndrome / physiopathology*
  • Pregnancy
  • Prenatal Exposure Delayed Effects / chemically induced
  • Prenatal Exposure Delayed Effects / physiopathology*
  • Testosterone

Substances

  • Lipids
  • Muscle Proteins
  • Testosterone