Whole-body metabolic fate of branched-chain amino acids

Biochem J. 2021 Feb 26;478(4):765-776. doi: 10.1042/BCJ20200686.

Abstract

Oxidation of branched-chain amino acids (BCAAs) is tightly regulated in mammals. We review here the distribution and regulation of whole-body BCAA oxidation. Phosphorylation and dephosphorylation of the rate-limiting enzyme, branched-chain α-ketoacid dehydrogenase complex directly regulates BCAA oxidation, and various other indirect mechanisms of regulation also exist. Most tissues throughout the body are capable of BCAA oxidation, and the flux of oxidative BCAA disposal in each tissue is influenced by three key factors: 1. tissue-specific preference for BCAA oxidation relative to other fuels, 2. the overall oxidative activity of mitochondria within a tissue, and 3. total tissue mass. Perturbations in BCAA oxidation have been implicated in many disease contexts, underscoring the importance of BCAA homeostasis in overall health.

Keywords: branched chain amino acids; isoleucine; leucine; organismal metabolism; valine.

MeSH terms

  • 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) / metabolism*
  • Amino Acids, Branched-Chain / metabolism*
  • Animals
  • Bacterial Proteins / metabolism
  • Decarboxylation
  • Female
  • Forecasting
  • Heart Failure / metabolism
  • Humans
  • Insulin Resistance / physiology
  • Male
  • Maple Syrup Urine Disease / genetics
  • Maple Syrup Urine Disease / metabolism
  • Mitochondria / metabolism
  • Mitochondrial Membranes / enzymology
  • Multienzyme Complexes
  • Neoplasm Proteins / metabolism
  • Neoplasms / metabolism
  • Organ Specificity
  • Oxidation-Reduction
  • Phosphorylation
  • Plant Proteins / metabolism
  • Protein Processing, Post-Translational

Substances

  • Amino Acids, Branched-Chain
  • Bacterial Proteins
  • Multienzyme Complexes
  • Neoplasm Proteins
  • Plant Proteins
  • 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)