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The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes

INTRODUCTION: Deregulation of adipogenesis plays an important role in obesity and other metabolism disorders. PPAR, C/EBP and SREBP1c are key transcriptional factors involved in adipogenesis and lipogenesis. Juglanin is a natural compound belonging to flavonoids, and it has been reported that juglan...

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Autores principales: Wang, Guang, Wu, Bing, Xu, Wenzhou, Jin, Xuefei, Wang, Kun, Wang, Heyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719332/
https://www.ncbi.nlm.nih.gov/pubmed/33293796
http://dx.doi.org/10.2147/DDDT.S256504
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author Wang, Guang
Wu, Bing
Xu, Wenzhou
Jin, Xuefei
Wang, Kun
Wang, Heyuan
author_facet Wang, Guang
Wu, Bing
Xu, Wenzhou
Jin, Xuefei
Wang, Kun
Wang, Heyuan
author_sort Wang, Guang
collection PubMed
description INTRODUCTION: Deregulation of adipogenesis plays an important role in obesity and other metabolism disorders. PPAR, C/EBP and SREBP1c are key transcriptional factors involved in adipogenesis and lipogenesis. Juglanin is a natural compound belonging to flavonoids, and it has been reported that juglanin has a potent inhibitory effect on inflammation and certain type of cancers. However, the effects of juglanin in adipogenesis have not been reported before. MATERIALS AND METHODS: 3T3-L1 preadipocytes were incubated with differentiation induction medium in the presence or absence of 0.5, 2.5, or 5 µM juglanin for an 8-day differentiation period. The lipid droplets accumulated in the cytoplasm were monitored by Oil Red O staining on days 0, 2, 5, and 8. The regulatory effects of juglanin on adipogenesis-related genes and proteins were investigated by real-time polymerase chain reaction and Western blot analysis. RESULTS: Juglanin significantly decreased lipid accumulation in differentiated adipocytes. Our findings show that juglanin reduced the expression of C/EBPα, C/EBPβ, and SREBP-1c without affecting PPARα or PPARγ expression. Additionally, juglanin increased the activation of the SIRT1/AMPK signaling pathway through the phosphorylation of AMPKα. Finally, we performed an AMPK inhibitor experiment, which revealed that the inhibitory effects of juglanin on adipogenesis are mediated through AMPK. DISCUSSION: Juglanin can prevent adipogenesis by suppressing lipid accumulation and the differentiation of preadipocytes. The mechanism of juglanin regulating adipogenesis requires further investigation. Future clinical study in vivo could shed more light on its implication in modulating obesity and metabolic disorders.
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spelling pubmed-77193322020-12-07 The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes Wang, Guang Wu, Bing Xu, Wenzhou Jin, Xuefei Wang, Kun Wang, Heyuan Drug Des Devel Ther Original Research INTRODUCTION: Deregulation of adipogenesis plays an important role in obesity and other metabolism disorders. PPAR, C/EBP and SREBP1c are key transcriptional factors involved in adipogenesis and lipogenesis. Juglanin is a natural compound belonging to flavonoids, and it has been reported that juglanin has a potent inhibitory effect on inflammation and certain type of cancers. However, the effects of juglanin in adipogenesis have not been reported before. MATERIALS AND METHODS: 3T3-L1 preadipocytes were incubated with differentiation induction medium in the presence or absence of 0.5, 2.5, or 5 µM juglanin for an 8-day differentiation period. The lipid droplets accumulated in the cytoplasm were monitored by Oil Red O staining on days 0, 2, 5, and 8. The regulatory effects of juglanin on adipogenesis-related genes and proteins were investigated by real-time polymerase chain reaction and Western blot analysis. RESULTS: Juglanin significantly decreased lipid accumulation in differentiated adipocytes. Our findings show that juglanin reduced the expression of C/EBPα, C/EBPβ, and SREBP-1c without affecting PPARα or PPARγ expression. Additionally, juglanin increased the activation of the SIRT1/AMPK signaling pathway through the phosphorylation of AMPKα. Finally, we performed an AMPK inhibitor experiment, which revealed that the inhibitory effects of juglanin on adipogenesis are mediated through AMPK. DISCUSSION: Juglanin can prevent adipogenesis by suppressing lipid accumulation and the differentiation of preadipocytes. The mechanism of juglanin regulating adipogenesis requires further investigation. Future clinical study in vivo could shed more light on its implication in modulating obesity and metabolic disorders. Dove 2020-12-02 /pmc/articles/PMC7719332/ /pubmed/33293796 http://dx.doi.org/10.2147/DDDT.S256504 Text en © 2020 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Guang
Wu, Bing
Xu, Wenzhou
Jin, Xuefei
Wang, Kun
Wang, Heyuan
The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title_full The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title_fullStr The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title_full_unstemmed The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title_short The Inhibitory Effects of Juglanin on Adipogenesis in 3T3-L1 Adipocytes
title_sort inhibitory effects of juglanin on adipogenesis in 3t3-l1 adipocytes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719332/
https://www.ncbi.nlm.nih.gov/pubmed/33293796
http://dx.doi.org/10.2147/DDDT.S256504
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