Uvaol ameliorates lipid deposition in hyperlipidemic hepatocytes by suppressing protein-tyrosine phosphatase 1B/ER stress signaling

Biochem Biophys Res Commun. 2024 Oct 20:730:150387. doi: 10.1016/j.bbrc.2024.150387. Epub 2024 Jul 10.

Abstract

Uvaol (UV), a pentacyclic triterpene found in olives and virgin olive oil, is known for its anti-inflammatory and antioxidant effects in various disease models. While olive oil is reported to reduce obesity and insulin resistance, the specific impact of UV on liver lipid metabolism and its molecular mechanisms are not fully understood. In this study, hepatic lipid accumulation was measured using oil red O staining, and protein expression levels in liver cells were assessed via Western blot analysis. Apoptosis was evaluated through cell viability and caspase 3 activity assays. UV treatment reduced lipid accumulation, fatty acid uptake, apoptosis, and ER stress in palmitate-treated liver cells. Additionally, UV enhanced fatty acid oxidation. Mechanistically, increased SIRT6 expression and autophagy were observed in UV-treated cells. SIRT6-targeted siRNA or 3-methyladenine blocked the effects of UV in hyperlipidemic cells. In conclusion, UV improves SIRT6/autophagy signaling, reducing lipid deposition and apoptosis in liver cells under high lipid conditions. This in vitro study provides strong evidence for potential therapeutic strategies for hepatic steatosis.

Keywords: Apoptosis; Autophagy; ER stress; Hepatic steatosis; SIRT6; Uvaol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Apoptosis* / radiation effects
  • Autophagy / drug effects
  • Endoplasmic Reticulum Stress* / drug effects
  • Hepatocytes* / drug effects
  • Hepatocytes* / metabolism
  • Hepatocytes* / radiation effects
  • Humans
  • Hyperlipidemias* / drug therapy
  • Hyperlipidemias* / metabolism
  • Lipid Metabolism* / drug effects
  • Pentacyclic Triterpenes / pharmacology
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / antagonists & inhibitors
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / genetics
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / metabolism
  • Signal Transduction* / drug effects
  • Sirtuins* / genetics
  • Sirtuins* / metabolism

Substances

  • Sirtuins
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Pentacyclic Triterpenes