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Original Articles

Lipogenesis inhibition and adipogenesis regulation via PPARγ pathway in 3T3-L1 cells by Zingiber cassumunar Roxb. rhizome extracts

, , , , , , & show all
Pages 289-297 | Received 15 Oct 2017, Accepted 08 Sep 2018, Published online: 06 Mar 2019
 

Abstract

Zingiber cassumunar (ZC) is used by tribal people in northern Thailand in traditional remedies for anti-obesity and in food recipes. Extracts from this plant have been studied for several pharmacological effects including anti-obesity, but with no clear evidence on cellular mechanism of activity. This study aim to investigate the lipolytic and anti-adipogenic activity of crude extracts from ZC on in vitro cultures of the mouse adipocyte cell-model, 3T3-L1. Dry rhizome powder was extracted with absolute ethanol and boiled-water. On the exposed pre-adipocytes to the extracts, cytotoxicity was not detected by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Lipid content and glycerol release were assessed using Oil Red-O and a commercial Adipolysis Assay kits respectively. The extracts exhibited no significant lipolytic activity on the exposed mature-adipocytes, in serial dilutions ranging from 1 to 800 µg/ml. However, anti-lipogenic activity was presented. All extracts significantly reduced the lipid content of exposed differentiating-adipocytes. This anti-lipogenic activity was confirmed by the expression of selected genes, determined by using real-time PCR techniques, in four groups namely: adipocyte differentiation genes, glucose uptake genes, lipid metabolism genes and fatty acid oxidation genes. 1H NMR spectrum of the extracts exhibited the prominent olefinic protons of phenylbutanoids, the group of compounds previously proved with several bioactivities. This study provided evidences of mechanisms that apparently verify the traditional use of ZC to prevent obesity.

Acknowledgements

We are very grateful to the National Research Council of Thailand (Project code: 130031-2556A10402008) for financial support of this study and to the Research Professional Development Project (under the Science Achievement Scholarship of Thailand (SAST)) for providing a Master degree scholarship to Mr. Natthawut Wong-a-nan. We also thank the Human and Animal Cell Technology Research Unit and Medicinal Plant and Reproductive Research Unit of the Department of Biology and the Department of Chemistry both in the Faculty of Science, Chiang Mai University and also for institutional support. Appreciation of supports are also belong to Chulabhorn Graduate Institute, Chemical Biology Program, Chulabhorn Royal Academy, and Chulabhorn Research Institute, Bangkok. Finally, we thanks Dr. Stephen Elliott for his kindly revision on the first draft and for lots of useful comments.

Conflict of interest statement

We declare that we have no conflict of interest.