Actions of short-term fasting on human skeletal muscle myogenic and atrogenic gene expression

Ann Nutr Metab. 2006;50(5):476-81. doi: 10.1159/000095354. Epub 2006 Aug 24.

Abstract

Background: Skeletal muscle mass is governed by multiple IGF-1-sensitive positive regulators of muscle-specific protein synthesis (myogenic regulatory factors which includes myoD, myogenin and Myf5) and negative regulators, including the atrogenic proteins myostatin, atrogin-1 and muscle ring finger 1 (MuRF-1). The coordinated control of these myogenic and atrogenic factors in human skeletal muscle following short-term fasting is currently unknown.

Method: Healthy adults (n = 6, age 27.6 years) undertook a 40-hour fast. Skeletal muscle biopsy (vastus lateralis) and venous blood samples were taken 3, 15 and 40 h into the fast after an initial standard high-carbohydrate meal. Gene expression of the myogenic regulator factors (myoD, myogenin and Myf5) and the atrogenic factors (myostatin, atrogin-1 and MuRF-1) were determined by real-time PCR analysis. Plasma myostatin and IGF-1 were determined by ELISA.

Results: There were no significant alterations in either the positive or negative regulators of muscle mass at either 15 or 40 h, when compared to gene expression measured 3 h after a meal. Similarly, plasma myostatin and IGF-1 were also unaltered at these times.

Conclusions: Unlike previous observations in catabolic and cachexic diseased states, short-term fasting (40 h) fails to elicit marked alteration of the genes regulating both muscle-specific protein synthesis or atrophy. Greater periods of fasting may be required to initiate coordinated inhibition of myogenic and atrogenic gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biopsy, Needle
  • Fasting / metabolism*
  • Female
  • Gene Expression Regulation*
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / metabolism*
  • MyoD Protein / metabolism
  • Myogenic Regulatory Factor 5 / metabolism
  • Myogenic Regulatory Factors / metabolism*
  • Myogenin / metabolism
  • Myostatin
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / metabolism*
  • SKP Cullin F-Box Protein Ligases / metabolism
  • Time Factors
  • Transforming Growth Factor beta / blood
  • Transforming Growth Factor beta / metabolism
  • Tripartite Motif Proteins
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • MSTN protein, human
  • Muscle Proteins
  • MyoD Protein
  • Myogenic Regulatory Factor 5
  • Myogenic Regulatory Factors
  • Myogenin
  • Myostatin
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Tripartite Motif Proteins
  • Insulin-Like Growth Factor I
  • FBXO32 protein, human
  • SKP Cullin F-Box Protein Ligases
  • TRIM63 protein, human
  • Ubiquitin-Protein Ligases