α-Ketoglutarate prevents hyperlipidemia-induced fatty liver mitochondrial dysfunction and oxidative stress by activating the AMPK-pgc-1α/Nrf2 pathway

Redox Biol. 2024 Aug:74:103230. doi: 10.1016/j.redox.2024.103230. Epub 2024 Jun 13.

Abstract

α-Ketoglutarate (AKG), a crucial intermediate in the tricarboxylic acid cycle, has been demonstrated to mitigate hyperlipidemia-induced dyslipidemia and endothelial damage. While hyperlipidemia stands as a major trigger for non-alcoholic fatty liver disease, the protection of AKG on hyperlipidemia-induced hepatic metabolic disorders remains underexplored. This study aims to investigate the potential protective effects and mechanisms of AKG against hepatic lipid metabolic disorders caused by acute hyperlipidemia. Our observations indicate that AKG effectively alleviates hepatic lipid accumulation, mitochondrial dysfunction, and loss of redox homeostasis in P407-induced hyperlipidemia mice, as well as in palmitate-injured HepG2 cells and primary hepatocytes. Mechanistic insights reveal that the preventive effects are mediated by activating the AMPK-PGC-1α/Nrf2 pathway. In conclusion, our findings shed light on the role and mechanism of AKG in ameliorating abnormal lipid metabolic disorders in hyperlipidemia-induced fatty liver, suggesting that AKG, an endogenous mitochondrial nutrient, holds promising potential for addressing hyperlipidemia-induced fatty liver conditions.

Keywords: Fatty liver; Hyperlipidemia; Mitochondrial dysfunction; Nrf2; Oxidative stress; PGC-1α; α-Ketoglutarate (AKG).

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Animals
  • Disease Models, Animal
  • Fatty Liver / drug therapy
  • Fatty Liver / etiology
  • Fatty Liver / metabolism
  • Fatty Liver / pathology
  • Fatty Liver / prevention & control
  • Hep G2 Cells
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Humans
  • Hyperlipidemias* / complications
  • Hyperlipidemias* / drug therapy
  • Hyperlipidemias* / metabolism
  • Ketoglutaric Acids* / metabolism
  • Ketoglutaric Acids* / pharmacology
  • Lipid Metabolism / drug effects
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • NF-E2-Related Factor 2* / metabolism
  • Oxidative Stress* / drug effects
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha* / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha* / metabolism
  • Signal Transduction* / drug effects

Substances

  • NF-E2-Related Factor 2
  • AMP-Activated Protein Kinases
  • Ketoglutaric Acids
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha