Issue 11, 2014

The AMPK pathway mediates an anti-adipogenic effect of fruits of Hovenia dulcis Thunb.

Abstract

Hovenia dulcis Thunb. is well known as a treatment for liver disease. Several studies have demonstrated that extracts of Hovenia dulcis Thunb. or its purified compounds can serve as detoxifying agents for alcohol poisoning. However, its anti-obesity effect has not been reported thus far. In this study, the anti-obesity effect of water extracts from the fruits or stems of Hovenia dulcis Thunb. was examined in 3T3-L1 preadipocytes. The cellular lipid contents in 3T3-L1 adipocytes were assessed by Oil Red O staining. Fruits of Hovenia dulcis Thunb. (FHD) significantly inhibit lipid accumulation during adipogenesis in a dose-dependent manner, but not stems of Hovenia dulcis Thunb. FHD (100 μg ml−1) significantly down-regulates the expression of the peroxisome proliferator-activated receptor-γ, CCAAT/enhancer-binding protein-α, adipocyte fatty acid-binding protein 2, adiponectin, and resistin, and the inhibition rates were 29.33%, 54.36%, 34.5%, 55.69%, and 60.39%, respectively. In addition, FHD (100 μg ml−1) also up-regulates the phosphorylation of AMP-activated protein kinase (AMPK)-α, liver kinase B1 as a major AMPK kinase, and the downstream substrate acetyl-CoA carboxylase, and the inhibition rates were 43.52%, 38.25%, and 20.39%, respectively. These results indicate that FHD has a significant anti-obesity effect through the modulation of the AMPK pathway, suggesting that FHD has a potential benefit in preventing obesity.

Graphical abstract: The AMPK pathway mediates an anti-adipogenic effect of fruits of Hovenia dulcis Thunb.

Article information

Article type
Paper
Submitted
29 May 2014
Accepted
26 Aug 2014
First published
16 Sep 2014

Food Funct., 2014,5, 2961-2968

The AMPK pathway mediates an anti-adipogenic effect of fruits of Hovenia dulcis Thunb.

H. Kim, J. Sim, H. Choi, I. Choi, M. Jeong, J. Park, Y. Jung, D. Youn, J. Cho, J. Kim, M. Hwang, J. Jin, S. Hong, H. Cho and J. Um, Food Funct., 2014, 5, 2961 DOI: 10.1039/C4FO00470A

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