4.6 Article

Abietic acid alleviates endoplasmic reticulum stress and lipid accumulation in human primary hepatocytes through the AMPK/ORP150 signaling

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2022.04.010

Keywords

Abietic acid; ER stress; AMPK; ORP150; NAFLD

Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MSIT) [2022R1A2B5B01001453, 2021R1F1A1050004]
  2. Chung-Ang University Research Scholarship
  3. National Research Foundation of Korea [2022R1A2B5B01001453, 2021R1F1A1050004] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Abietic acid (AA), the main component of pine resin that has traditionally been used in Asian medicine, has anti-inflammatory activities. This study found that AA can reduce lipid accumulation in hepatocytes by suppressing endoplasmic reticulum stress, making it a potential candidate for treating non-alcoholic fatty liver disease.
Abietic acid (AA), the main component of pine resin that has been traditionally used as Asian medicine, has been reported to demonstrate anti-inflammatory activities. Despite this, little is known about the effects of AA on hepatic endoplasmic reticulum (ER) stress and lipid metabolism. This study investigated the impacts of AA on ER stress and steatosis in in vitro obesity models. We found that Treatment with AA reduced lipid deposition and lipogenesis-related proteins expression in human primary hepatocytes. Augmented expression of ER stress markers (phospho-eukaryotic initiation factor-2 alpha (eIF2 alpha) and C/EBP homologous protein (CHOP)) in palmitate-treated hepatocytes were reversed by AA treatment. Further, AA treatment increased the expression of phospho-AMPK and oxygen-regulated protein 150 (ORP150) in hepatocytes. siRNA-associated knockdown of AMPK or ORP150 expression reduced the effects of AA on not only hepatic ER stress but also lipogenesis and apoptosis. These results denote that AA attenuates lipid accumulation in hepatocytes in the presence of palmitate through the suppression of ER stress by AMPK/ORP150 signaling. AA could be a potential candidate for treating non-alcoholic fatty liver disease. (c) 2022 Elsevier Inc. All rights reserved.

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