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Idesolide inhibits the adipogenic differentiation of mesenchymal cells through the suppression of nitric oxide production

Authors
Hwang, Jun-HaMoon, Sung AhLee, Cham HanByun, Mi RanKim, A. RumSung, Mi KyungPark, Hyun-JinHwang, Eun SookSung, Sang HyunHong, Jeong-Ho
Issue Date
15-6월-2012
Publisher
ELSEVIER SCIENCE BV
Keywords
Obesity; Adipogenic differentiation; Nitric oxide; Idesolide
Citation
EUROPEAN JOURNAL OF PHARMACOLOGY, v.685, no.1-3, pp.218 - 223
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume
685
Number
1-3
Start Page
218
End Page
223
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108155
DOI
10.1016/j.ejphar.2012.04.018
ISSN
0014-2999
Abstract
Obesity is a major health problem worldwide and can increase the risk for several chronic diseases, including diabetes and cardiovascular disease. In this study, we screened small compounds isolated from natural products for the development of an anti-obesity drug. Among them, idesolide, a spiro compound isolated from the fruits of Idesia polycarpa Maxim, showed a significant suppression of the adipogenic differentiation in mesenchymal cells, as indicated by the decrease in fat droplets and expression of adipogenic marker genes such as aP2 and adiponectin. Idesolide inhibits the PPAR gamma-mediated gene transcription in a dose-dependent manner, revealed by luciferase reporter gene assay. During adipogenic differentiation, idesolide inhibits nitric oxide production through the suppression of iNOS expression, and the increased adipogenic differentiation by arginine, the substrate for NOS, is significantly inhibited by idesolide, suggesting that the inhibition of nitric oxide production plays a major role in idesolide-induced adipogenic suppression. Taken together, the results reveal that idesolide has anti-adipogenic activity and highlight its potential in the prevention and treatment of obesity. (C) 2012 Elsevier B. V. All rights reserved.
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