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Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes
BACKGROUND: An excess storage of body fat causes obesity. Since obesity increases risk of chronic diseases, it is important to inhibit excessive storage of fat. Zaluzanin C is a sesquiterpene lactone isolated from Ainsliaea acerifolia. The aim of this study was to demonstrate the effect of zaluzanin...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for the Study of Obesity
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604843/ https://www.ncbi.nlm.nih.gov/pubmed/31294342 http://dx.doi.org/10.7570/jomes.2019.28.2.105 |
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author | Kwak, Sang Hee Kim, Yoon Hee |
author_facet | Kwak, Sang Hee Kim, Yoon Hee |
author_sort | Kwak, Sang Hee |
collection | PubMed |
description | BACKGROUND: An excess storage of body fat causes obesity. Since obesity increases risk of chronic diseases, it is important to inhibit excessive storage of fat. Zaluzanin C is a sesquiterpene lactone isolated from Ainsliaea acerifolia. The aim of this study was to demonstrate the effect of zaluzanin C on differentiation of 3T3-L1 preadipocytes into mature adipocytes. METHODS: The cytotoxicity of zaluzanin C and its effect on cell proliferation was determined. For the induction of adipocyte differentiation, 3T3-L1 preadipocytes were treated with differentiating medium containing 10 μg/mL insulin, 115 μg/mL methylisobutylxanthine, and 1 μM dexamethasone. Differentiated 3T3-L1 cells were subjected to Oil red O solution or used for Western blot analysis. Zaluzanin C was added to the cell culture medium at concentrations of 0, 1, 2.5, 5, and 10 μM. RESULTS: Zaluzanin C did not inhibit cell proliferation and showed no cytotoxicity at 10 μM concentration in 3T3-L1 cells. Therefore, concentration range of 0–10 μM zaluzanin C was used for subsequent experiments. Zaluzanin C inhibited accumulation of lipid droplets in 3T3-L1 adipocytes. To understand the underlying mechanism of zaluzanin C, expression of adipogenesis regulators was determined by Western blot analysis. Zaluzanin C suppressed peroxisome proliferator-activated receptor gamma (PPARγ) expression, an adipogenesis related transcription factor, and inhibited aP2/fatty acid-binding protein-4 expression, a target gene of PPARγ. However, it did not affect expression of CCAAT/enhancer-binding protein alpha related with acquisition of insulin sensitivity. CONCLUSION: These data suggest that inhibitory effect of zaluzanin C on adipogenesis of 3T3-L1 adipocytes could be partially caused by suppressing PPARγ. |
format | Online Article Text |
id | pubmed-6604843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for the Study of Obesity |
record_format | MEDLINE/PubMed |
spelling | pubmed-66048432019-07-10 Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes Kwak, Sang Hee Kim, Yoon Hee J Obes Metab Syndr Original Article BACKGROUND: An excess storage of body fat causes obesity. Since obesity increases risk of chronic diseases, it is important to inhibit excessive storage of fat. Zaluzanin C is a sesquiterpene lactone isolated from Ainsliaea acerifolia. The aim of this study was to demonstrate the effect of zaluzanin C on differentiation of 3T3-L1 preadipocytes into mature adipocytes. METHODS: The cytotoxicity of zaluzanin C and its effect on cell proliferation was determined. For the induction of adipocyte differentiation, 3T3-L1 preadipocytes were treated with differentiating medium containing 10 μg/mL insulin, 115 μg/mL methylisobutylxanthine, and 1 μM dexamethasone. Differentiated 3T3-L1 cells were subjected to Oil red O solution or used for Western blot analysis. Zaluzanin C was added to the cell culture medium at concentrations of 0, 1, 2.5, 5, and 10 μM. RESULTS: Zaluzanin C did not inhibit cell proliferation and showed no cytotoxicity at 10 μM concentration in 3T3-L1 cells. Therefore, concentration range of 0–10 μM zaluzanin C was used for subsequent experiments. Zaluzanin C inhibited accumulation of lipid droplets in 3T3-L1 adipocytes. To understand the underlying mechanism of zaluzanin C, expression of adipogenesis regulators was determined by Western blot analysis. Zaluzanin C suppressed peroxisome proliferator-activated receptor gamma (PPARγ) expression, an adipogenesis related transcription factor, and inhibited aP2/fatty acid-binding protein-4 expression, a target gene of PPARγ. However, it did not affect expression of CCAAT/enhancer-binding protein alpha related with acquisition of insulin sensitivity. CONCLUSION: These data suggest that inhibitory effect of zaluzanin C on adipogenesis of 3T3-L1 adipocytes could be partially caused by suppressing PPARγ. Korean Society for the Study of Obesity 2019-06 2019-06-30 /pmc/articles/PMC6604843/ /pubmed/31294342 http://dx.doi.org/10.7570/jomes.2019.28.2.105 Text en Copyright © 2019 Korean Society for the Study of Obesity This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kwak, Sang Hee Kim, Yoon Hee Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title | Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title_full | Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title_fullStr | Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title_full_unstemmed | Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title_short | Zaluzanin C Inhibits Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes |
title_sort | zaluzanin c inhibits differentiation of 3t3-l1 preadipocytes into mature adipocytes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604843/ https://www.ncbi.nlm.nih.gov/pubmed/31294342 http://dx.doi.org/10.7570/jomes.2019.28.2.105 |
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