The New Therapeutic Approaches in the Treatment of Non-Alcoholic Fatty Liver Disease

Int J Mol Sci. 2021 Dec 8;22(24):13219. doi: 10.3390/ijms222413219.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease which is characterized by extremely complex pathogenetic mechanisms and multifactorial etiology. Some of the many pathophysiological mechanisms involved in the development of NAFLD include oxidative stress, impaired mitochondrial metabolism, inflammation, gut microbiota, and interaction between the brain-liver-axis and the regulation of hepatic lipid metabolism. The new therapeutic approaches in the treatment of NAFLD are targeting some of these milestones along the pathophysiological pathway and include drugs like agonists of peroxisome proliferator-activated receptors (PPARs), glucagon-like peptide-1 (GLP-1) agonists, sodium/glucose transport protein 2 (SGLT2) inhibitors, farnesoid X receptor (FXR) agonists, probiotics, and symbiotics. Further efforts in biomedical sciences should focus on the investigation of the relationship between the microbiome, liver metabolism, and response to inflammation, systemic consequences of metabolic syndrome.

Keywords: dysbiosis; lipotoxicity; new therapeutic modalities; non-alcoholic fatty liver disease; organelle dysfunction.

Publication types

  • Review

MeSH terms

  • Gastrointestinal Microbiome / drug effects
  • Glucagon-Like Peptide 1 / agonists
  • Humans
  • Lipid Metabolism / drug effects
  • Molecular Targeted Therapy / methods*
  • Non-alcoholic Fatty Liver Disease / drug therapy*
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Non-alcoholic Fatty Liver Disease / microbiology*
  • Oxidative Stress / drug effects
  • Peroxisome Proliferator-Activated Receptors / agonists
  • Probiotics / pharmacology
  • Probiotics / therapeutic use
  • Sodium-Glucose Transporter 2 Inhibitors / pharmacology
  • Sodium-Glucose Transporter 2 Inhibitors / therapeutic use

Substances

  • Peroxisome Proliferator-Activated Receptors
  • Sodium-Glucose Transporter 2 Inhibitors
  • Glucagon-Like Peptide 1