The Role of Reduced Methionine in Mediating the Metabolic Responses to Protein Restriction Using Different Sources of Protein

Nutrients. 2021 Jul 29;13(8):2609. doi: 10.3390/nu13082609.

Abstract

Dietary protein restriction and dietary methionine restriction (MR) produce a comparable series of behavioral, physiological, biochemical, and transcriptional responses. Both dietary regimens produce a similar reduction in intake of sulfur amino acids (e.g., methionine and cystine), and both diets increase expression and release of hepatic FGF21. Given that FGF21 is an essential mediator of the metabolic phenotype produced by both diets, an important unresolved question is whether dietary protein restriction represents de facto methionine restriction. Using diets formulated from either casein or soy protein with matched reductions in sulfur amino acids, we compared the ability of the respective diets to recapitulate the metabolic phenotype produced by methionine restriction using elemental diets. Although the soy-based control diets supported faster growth compared to casein-based control diets, casein-based protein restriction and soy-based protein restriction produced comparable reductions in body weight and fat deposition, and similar increases in energy intake, energy expenditure, and water intake. In addition, the prototypical effects of dietary MR on hepatic and adipose tissue target genes were similarly regulated by casein- and soy-based protein restriction. The present findings support the feasibility of using restricted intake of diets from various protein sources to produce therapeutically effective implementation of dietary methionine restriction.

Keywords: FGF21; essential amino acid; gene set enrichment; nutrient sensing; protein restriction.

MeSH terms

  • Adipose Tissue / metabolism
  • Amino Acids, Essential
  • Amino Acids, Sulfur
  • Animals
  • Body Weight
  • Caseins
  • Diet, Protein-Restricted*
  • Eating
  • Energy Intake
  • Energy Metabolism / physiology
  • Fibroblast Growth Factors / metabolism
  • Gene Expression
  • Humans
  • Liver / metabolism
  • Male
  • Methionine / metabolism*
  • Methionine / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Soybean Proteins
  • Transcriptome

Substances

  • Amino Acids, Essential
  • Amino Acids, Sulfur
  • Caseins
  • Soybean Proteins
  • fibroblast growth factor 21
  • Fibroblast Growth Factors
  • Methionine