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Uvaol ameliorates lipid deposition in hyperlipidemic hepatocytes by suppressing protein-tyrosine phosphatase 1B/ER stress signaling.
Gwon, Hyeon Ji; Chung, Yoon Hee; Lim, Do Su; Cho, Wonjun; Choi, Sung Woo; Abd El-Aty, A M; Song, Jin-Ho; Shin, Yong Kyoo; Jeong, Ji Hoon; Jung, Tae Woo.
Affiliation
  • Gwon HJ; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea; Department of Global Innovative Drugs, Graduate School of Chung-Ang University, Seoul, Republic of Korea.
  • Chung YH; Department of Anatomy, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
  • Lim DS; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea; Department of Global Innovative Drugs, Graduate School of Chung-Ang University, Seoul, Republic of Korea.
  • Cho W; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
  • Choi SW; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
  • Abd El-Aty AM; Department of Pharmacology, Faculty of Veterinary Medicine, Cairo University, 12211, Giza, Egypt; Department of Medical Pharmacology, Medical Faculty, Ataturk University, Erzurum, 25240, Turkey. Electronic address: abdelaty44@hotmail.com.
  • Song JH; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
  • Shin YK; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
  • Jeong JH; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea; Department of Global Innovative Drugs, Graduate School of Chung-Ang University, Seoul, Republic of Korea. Electronic address: jhjeong3@cau.ac.kr.
  • Jung TW; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea. Electronic address: twjung@cau.ac.kr.
Biochem Biophys Res Commun ; 730: 150387, 2024 10 20.
Article in En | MEDLINE | ID: mdl-39002201
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.
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Full text: 1 Database: MEDLINE Main subject: Signal Transduction / Apoptosis / Hepatocytes / Sirtuins / Lipid Metabolism / Endoplasmic Reticulum Stress / Hyperlipidemias Limits: Animals / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Signal Transduction / Apoptosis / Hepatocytes / Sirtuins / Lipid Metabolism / Endoplasmic Reticulum Stress / Hyperlipidemias Limits: Animals / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2024 Type: Article