Isoflavin-β modifies muscle oxidative stress and prevents a thyrotoxicosis-induced loss of muscle mass in rats

Muscle Nerve. 2017 Nov;56(5):975-981. doi: 10.1002/mus.25546. Epub 2017 Mar 24.

Abstract

Introduction: We sought to verify whether isoflavin-beta (Iso-β), a mixture of isoflavones with antioxidant properties, could prevent thyrotoxicosis-induced loss of muscle mass and the participation of oxidative stress (OS) in the mechanisms of this prevention.

Methods: Two experimental periods of thyrotoxicosis induction were used in Wistar rats: 3 and 5 days to assess Iso-β effects before and after thyrotoxicosis-induced muscle wasting. After euthanasia, peritoneal fat and gastrocnemius muscle were collected, weighed, and muscle OS was assessed.

Results: Iso-β prevented the loss of gastrocnemius mass in thyrotoxic rats through the prevention of muscle OS generation during thyrotoxicosis, increasing muscle total antioxidant capacity and decreasing mitochondrial cytochrome c oxidase activity, lipid peroxidation, and protein carbonyl content.

Conclusion: Iso-β decreased oxidative modification of proteins, which is known to exert a major role during proteolysis induction and is present in thyrotoxic myopathy, highlighting the potential action of Iso-β in this complication of the disease. Muscle Nerve 56: 975-981, 2017.

Keywords: isoflavin-β; isoflavones; muscle proteolysis; myopathy; thyrotoxicosis.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use*
  • Chymotrypsin / metabolism
  • Cyclohexanols / blood
  • Cyclohexanols / toxicity
  • Disease Models, Animal
  • Drug Administration Schedule
  • Electron Transport Complex IV / metabolism
  • Glycerol / blood
  • Isoflavones / pharmacology
  • Isoflavones / therapeutic use*
  • Male
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / pathology
  • Muscular Atrophy
  • Oxidative Stress / drug effects*
  • Protein Carbonylation / drug effects
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Thyrotoxicosis / blood
  • Thyrotoxicosis / chemically induced
  • Thyrotoxicosis / pathology*
  • Thyrotoxicosis / prevention & control*
  • tert-Butylhydroperoxide / metabolism

Substances

  • Antioxidants
  • Cyclohexanols
  • Isoflavones
  • Thiobarbituric Acid Reactive Substances
  • 3,3,5-trimethylcyclohexanol
  • tert-Butylhydroperoxide
  • Superoxide Dismutase
  • Electron Transport Complex IV
  • Chymotrypsin
  • Glycerol