Propofol ameliorates acute postoperative fatigue and promotes glucagon-regulated hepatic gluconeogenesis by activating CREB/PGC-1α and accelerating fatty acids beta-oxidation

Biochem Biophys Res Commun. 2022 Jan 1:586:121-128. doi: 10.1016/j.bbrc.2021.11.073. Epub 2021 Nov 23.

Abstract

Postoperative fatigue (POF) is the most common and long-lasting complication after surgery, which brings heavy burden to individuals and society. Recently, hastening postoperative recovery receives increasing attention, but unfortunately, the mechanisms underlying POF remain unclear. Propofol is a wildly used general anesthetic in clinic, and inspired by the rapid antidepressant effects induced by ketamine at non-anesthetic dose, the present study was undertaken to investigate the anti-fatigue effects and underlying mechanisms of propofol at a non-anesthetic dose in 70% hepatectomy induced POF model in rats. We first showed here that single administration of propofol at 0.1 mg/kg ameliorated acute POF in hepatectomy induced POF rats. Based on metabonomics analysis, we hypothesized that propofol exerted anti-fatigue activity in POF rats by facilitating free fatty acid (FFA) oxidation and gluconeogenesis. We further confirmed that propofol restored the deficit in FFA oxidation and gluconeogenesis in POF rats, as evidenced by the elevated FFA utilization, acetyl coenzyme A content, pyruvic acid content, phosphoenolpyruvic acid content, hepatic glucose output and glycogen storage. Moreover, propofol stimulated glucagon secretion and up-regulated expression of cAMP-response element binding protein (CREB), phosphorylated CREB, peroxlsome prolifeator-activated receptor-γ coactivator-1α (PGC-1α), phosphoenolpyruvate carboxykinade1 and carnitine palmitoltransferase 1A. In summary, our study suggests for the first time that propofol ameliorates acute POF by promoting glucagon-regulated gluconeogenesis via CREB/PGC-1α signaling and accelerating FFA beta-oxidation.

Keywords: Beta-oxidation; Free fatty acids; Gluconeogenesis; Postoperative fatigue; Propofol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Animals
  • CREB-Binding Protein / genetics
  • CREB-Binding Protein / metabolism
  • Carnitine O-Palmitoyltransferase / genetics
  • Carnitine O-Palmitoyltransferase / metabolism
  • Fatigue / genetics
  • Fatigue / metabolism
  • Fatigue / physiopathology
  • Fatigue / prevention & control*
  • Fatty Acids, Nonesterified / metabolism*
  • Gene Expression Regulation
  • Gluconeogenesis / drug effects*
  • Gluconeogenesis / genetics
  • Hepatectomy / methods
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Hypnotics and Sedatives / pharmacology*
  • Lipid Metabolism / drug effects
  • Lipid Metabolism / genetics
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / surgery
  • Male
  • Oxidation-Reduction
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism
  • Phosphoenolpyruvate / metabolism
  • Phosphoenolpyruvate Carboxykinase (ATP) / genetics
  • Phosphoenolpyruvate Carboxykinase (ATP) / metabolism
  • Postoperative Complications / genetics
  • Postoperative Complications / metabolism
  • Postoperative Complications / physiopathology
  • Propofol / pharmacology*
  • Pyruvic Acid / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Fatty Acids, Nonesterified
  • Hypnotics and Sedatives
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, rat
  • Acetyl Coenzyme A
  • Phosphoenolpyruvate
  • Pyruvic Acid
  • Carnitine O-Palmitoyltransferase
  • CREB-Binding Protein
  • Crebbp protein, rat
  • Phosphoenolpyruvate Carboxykinase (ATP)
  • Propofol