Differential developmental programming by early protein restriction of rat skeletal muscle according to its fibre-type composition

Acta Physiol (Oxf). 2014 Jan;210(1):70-83. doi: 10.1111/apha.12073. Epub 2013 Mar 11.

Abstract

Aims: Differences in fibre-type composition of skeletal muscle have been associated with obesity and insulin resistance. As a poor nutrient environment early in life is a predisposing factor for the development of obesity and related metabolic diseases at adulthood, this study aimed at determining the long-term consequences of maternal undernutrition on the structural and metabolic properties of two skeletal muscles characterized by their different fibre-type composition and metabolic properties.

Methods: The fibre-type composition and enzymatic activities of hexokinase (HK), beta-hydroxyacyl-CoA dehydrogenase (β-HAD) and citrate synthase (CS) were measured in soleus and extensor digitorum longus (EDL) muscles from adult rats born to dams fed a control (17% protein) or a low-protein [8% protein (PR)] diet throughout pregnancy and lactation. In addition, the expression levels of several genes regulating glycolysis, fatty acid oxidation and mitochondrial biogenesis were determined by real-time PCR.

Results: Protein rats exhibited enhanced density of type II fibres along with decreased rate of fatty acid oxidation and glycolysis in soleus but not EDL. Malnourished rats exhibited also a different gene expression profile in soleus and EDL. Altogether, these alterations correspond to a state of energy deficiency and are present in animals which do not show yet any sign of obesity or glucose intolerance.

Conclusion: We conclude that maternal protein restriction alters in the long term the structural and enzymatic properties of offspring skeletal muscle in a fibre-type-dependent manner. These alterations might have a causative role in the development of obesity and related metabolic disorders later in life.

Keywords: developmental programming; metabolism; skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / metabolism
  • Aging / metabolism*
  • Aging / pathology
  • Animals
  • Citrate (si)-Synthase / metabolism
  • Diet, Protein-Restricted*
  • Dietary Proteins / metabolism
  • Female
  • Hexokinase / metabolism
  • Male
  • Muscle Fibers, Fast-Twitch / enzymology*
  • Muscle Fibers, Fast-Twitch / pathology*
  • Muscle Fibers, Slow-Twitch / enzymology*
  • Muscle Fibers, Slow-Twitch / pathology*
  • Muscle Proteins / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Dietary Proteins
  • Muscle Proteins
  • 3-Hydroxyacyl CoA Dehydrogenases
  • Citrate (si)-Synthase
  • Hexokinase