作者 Seo, Min Suk; Hong, Sung-Woon; Yeon, Sung Hum; Kim, Young-Mok; Um, Key An; Kim, Jung Hwan; Kim, Hye Jung; Chang, Ki Churl; Park, Sang Won
期刊 JOURNAL OF ETHNOPHARMACOLOGY , NOV 18 2014,:157
DOI 10.1016/j.jep.2014.09.031 PubMed 25261688
摘要 Ethnopharmacological relevance: Magnolia officinalis (MO) is a traditional Chinese herbal medicine that has been used in clinical practice to treat liver disease. The aim of this study is to examine the effects of MO on the development of nonalcoholic fatty liver in hepatocytes.Materials and methods: Human hepatoma-derived HepG2 cells and mouse normal FL83B hepatocytes were exposed to 0.5 mM free fatty acids (FFAs; oleate:palmitate, 2:1) for 24 h to simulate conditions of nonalcoholic fatty liver in vitro. The cells were treated with a standardized MO extract 1 h prior to FFA exposure.Results: MO pretreatment attenuated the increases in intracellular lipid accumulation and triglyceride content in FFA-exposed hepatocytes in a dose-dependent manner. MO pretreatment significantly inhibited both sterol regulatory element-binding protein (SREBP)-1c activation and increases in fatty acid translocase, fatty acid synthase, and stearoyl CoA desaturase-1 protein expression in FFA-exposed hepatocytes in a dose-dependent manner. MO pretreatment markedly induced adenosine monophosphate-activated protein kinase (AMPK) phosphorylation in hepatocytes. Compound C, an AMPK inhibitor, blocked the inhibitory effect of MO on the increases in intracellular lipid accumulation and triglyceride content induced by FFAs. In hepatocytes pretreated with compound C, MO failed to inhibit SREBP-1c activation and the increases in fatty acid translocase, fatty acid synthase, and stearoyl-CoA desaturase-1 protein expression induced by FFAs.Conclusions: Our results indicate that MO attenuates triglyceride biosynthesis and accumulation induced by FFAs in hepatocytes, suggesting its pharmacological potential for the prevention of nonalcoholic fatty liver disease. These effects may be mediated by the inhibition of SREBP-1c via AMPK phosphorylation. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
版权所有 Copyright © 2002-2025 中国科学院昆明植物研究所,All Rights Reserved 【滇ICP备05000394号】
地址:中国云南省昆明市蓝黑路132号 邮政编码:650201 点击这里联系我们