Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Open AccessResearch

Stimulation of Apolipoprotein A-IV expression in Caco-2/TC7 enterocytes and reduction of triglyceride formation in 3T3-L1 adipocytes by potential anti-obesity Chinese herbal medicines

Ava Jiangyang Guo1 email, Roy Chi-yan Choi1 email, Anna Wing-han Cheung1 email, Jun Li1 email, Ivy Xiaoying Chen1 email, Tina Tingxia Dong1 email, Karl Wah-keung Tsim1 email and Brad Wing-chuen Lau2 email

Department of Biology and the Center for Chinese Medicine, Hong Kong University of Science and Technology, Clear Water Bay Road, Hong Kong SAR, PR China

Macao Institute for Applied Research in Medicine and Health (MUST Foundation), Avenida Wai Long, Taipa, Macao SAR, PR China

author email corresponding author email

Chinese Medicine 2009, 4:5doi:10.1186/1749-8546-4-5

Published: 26 March 2009

Abstract

Background

Chinese medicine has been proposed as a novel strategy for the prevention of metabolic disorders such as obesity. The present study tested 17 Chinese medicinal herbs were tested for their potential anti-obesity effects.

Methods

The herbs were evaluated in terms of their abilities to stimulate the transcription of Apolipoprotein A-IV (ApoA-IV) in cultured Caco-2/TC7 enterocytes. The herbs that showed stimulating effects on ApoA-IV transcription were further evaluated in terms of their abilities to reduce the formation of triglyceride in differentiated 3T3-L1 adipocytes.

Results

ApoA-IV transcription was stimulated by Rhizoma Alismatis and Radix Angelica Sinensis in a dose- and time-dependent manner in cultured Caco-2/TC7 cells. Moreover, these two herbs reduced the amount of triglyceride in differentiated 3T3-L1 adipocytes.

Conclusion

The results suggest that Rhizoma Alistmatis and Radix Angelica Sinensis may have potential anti-obesity effects as they stimulate ApoA-IV transcription and reduce triglyceride formation.


© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.