Amino Acids Regulate Glycolipid Metabolism and Alter Intestinal Microbial Composition

Curr Protein Pept Sci. 2020;21(8):761-765. doi: 10.2174/1389203721666200219100216.

Abstract

Amino acids (AAs) and their metabolites regulate key metabolic pathways that are necessary for growth, reproduction, immunity and metabolism of the body. It has been convinced that metabolic diseases are closely related to disorders of glycolipid metabolism. A growing number of studies have shown that AAs are closely related to energy metabolism. This review focuses on the effects of amino acids (arginine, branched-chain amino acids, glutamine) and their metabolites (short chain fatty acids) on glycolipid metabolism by regulating PI3K/AKT/mTOR and AMPK signaling pathways and GPCRs receptors, reducing intestinal Firmicutes/Bacteroidetes ratio associated with obesity.

Keywords: Glycolipid metabolism; amino acids (AAs); intestinal microbial composition; metabolic pathways; metabolites; short chain fatty acids (SCFAs).

Publication types

  • Review

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Amino Acids, Branched-Chain / metabolism
  • Amino Acids, Branched-Chain / pharmacology*
  • Bacteroidetes / drug effects
  • Bacteroidetes / physiology
  • Energy Metabolism / drug effects
  • Energy Metabolism / genetics
  • Fatty Acids, Volatile / metabolism
  • Firmicutes / drug effects
  • Firmicutes / physiology
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / physiology
  • Gene Expression Regulation*
  • Glycolipids / metabolism*
  • Humans
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / microbiology
  • Lipid Metabolism / drug effects*
  • Lipid Metabolism / genetics
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / microbiology
  • Obesity / pathology
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Amino Acids, Branched-Chain
  • Fatty Acids, Volatile
  • Glycolipids
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases