Protein lysine acetylation does not contribute to the high rates of fatty acid oxidation seen in the post-ischemic heart

Sci Rep. 2024 Jan 12;14(1):1193. doi: 10.1038/s41598-024-51571-0.

Abstract

High rates of cardiac fatty acid oxidation during reperfusion of ischemic hearts contribute to contractile dysfunction. This study aimed to investigate whether lysine acetylation affects fatty acid oxidation rates and recovery in post-ischemic hearts. Isolated working hearts from Sprague Dawley rats were perfused with 1.2 mM palmitate and 5 mM glucose and subjected to 30 min of ischemia and 40 min of reperfusion. Cardiac function, fatty acid oxidation, glucose oxidation, and glycolysis rates were compared between pre- and post-ischemic hearts. The acetylation status of enzymes involved in cardiac energy metabolism was assessed in both groups. Reperfusion after ischemia resulted in only a 41% recovery of cardiac work. Fatty acid oxidation and glycolysis rates increased while glucose oxidation rates decreased. The contribution of fatty acid oxidation to ATP production and TCA cycle activity increased from 90 to 93% and from 94.9 to 98.3%, respectively, in post-ischemic hearts. However, the overall acetylation status and acetylation levels of metabolic enzymes did not change in response to ischemia and reperfusion. These findings suggest that acetylation may not contribute to the high rates of fatty acid oxidation and reduced glucose oxidation observed in post-ischemic hearts perfused with high levels of palmitate substrate.

MeSH terms

  • Acetylation
  • Animals
  • Fatty Acids / metabolism
  • Glucose / metabolism
  • Glycolysis / physiology
  • Heart / physiology
  • Ischemia / metabolism
  • Lysine* / metabolism
  • Myocardium* / metabolism
  • Oxidation-Reduction
  • Palmitates / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Lysine
  • Fatty Acids
  • Glucose
  • Palmitates