6-Acetyl-2,2-Dimethylchroman-4-One Isolated from Artemisia princeps Suppresses Adipogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stromal Cells via Activation of AMPK

Obesity is a world-wide health concern with increasing mortality and morbidity rates. Development of novel therapeutic agents for obesity from phytochemicals may lead to the effective prevention and control of obesity and obesity-related complications. 6-acetyl-2,2-dimethylchroman-4-one ( ) was isol...

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Bibliographic Details
Published inJournal of medicinal food Vol. 23; no. 3; p. 250
Main Authors Karadeniz, Fatih, Oh, Jung Hwan, Lee, Jung Im, Kim, Hojun, Seo, Youngwan, Kong, Chang-Suk
Format Journal Article
LanguageEnglish
Published United States 01.03.2020
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Summary:Obesity is a world-wide health concern with increasing mortality and morbidity rates. Development of novel therapeutic agents for obesity from phytochemicals may lead to the effective prevention and control of obesity and obesity-related complications. 6-acetyl-2,2-dimethylchroman-4-one ( ) was isolated from a dietary plant, . The antiobesity effect of compound was determined in human bone marrow-derived mesenchymal stromal cells (hBM-MSCs) induced to differentiate into adipocytes. Treatment with compound resulted in decreased lipid accumulation and expression of key adipogenic markers, proliferator-activated receptor- , CCAAT/enhancer-binding protein- , and sterol regulatory element-binding transcription factor 1. It was also shown that compound downregulated the adipogenesis-induced p38 and JNK MAPK activation, while upregulating adipogenesis inhibitory -catenin-dependent Wnt10b pathway. Compound was also able to stimulate adenosine monophosphate-activated protein kinase phosphorylation, which was suggested to be the underlying mechanism that resulted in inhibition of adipogenesis in hBM-MSCs. In conclusion, 6-acetyl-2,2-dimethylchroman-4-one was identified as a bioactive constituent of that exerts antiobesity properties suppressing adipocyte formation.
ISSN:1557-7600
DOI:10.1089/jmf.2019.4653