Lose Weight with Traditional Chinese Medicine? Potential Suppression of Fat Mass and Obesity-Associated Protein

被引:19
作者
Chang, Pei-Chun [1 ]
Wang, Jing-Doo [1 ]
Lee, Min-Min [1 ]
Chang, Su-Sen [2 ]
Tsai, Tsung-Ying [2 ]
Chang, Kai-Wei [2 ]
Tsai, Fuu-Jen [1 ,2 ]
Chen, Calvin Yu-Chian [1 ,2 ,3 ,4 ,5 ]
机构
[1] Asia Univ, Dept Bioinformat, Taichung 41354, Taiwan
[2] China Med Univ, Sch Chinese Med, Lab Computat & Syst Biol, Taichung 40402, Taiwan
[3] China Med Univ, Beigang Hosp, Yunlin, Taiwan
[4] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[5] MIT, Cambridge, MA 02139 USA
关键词
Obesity; Traditional Chinese Medicine (TCM); FTO; Docking; Molecular Dynamics; FTO GENE; COMMON VARIANT; BLOOD-PRESSURE; EXPRESSION; DISCOVERY; CELLS; RISK; ADIPOSITY; DYNAMICS; ENERGY;
D O I
10.1080/07391102.2011.10507399
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Overweight and obesity are common health problems in modern society, particularly in developed countries. Excessive body mass has been linked to numerous diseases, such as cardiovascular diseases, diabetes, and cancer. Fat mass and obesity-associated protein (FTO) activity have direct impact on food intake and results in obesity. Inhibition of FTO activity may cause weight loss and reduce obese-linked health risks. We investigated the potential weight loss effects of traditional Chinese medicine (TCM), particularly by inhibiting FTO functions. Molecular docking was performed to screen TCM compounds from TCM Database@Taiwan (http://tcm.cmu.edu.tw). Three candidates were identified that contained either a tetrahydropyridine group or potent electronegative phenol group in the structure scaffold. Molecular dynamics simulation analysis of the docking poses of each complex indicated stabilizing trends in the protein-ligand complex movements. In addition, the number of hydrogen bonds increased throughout the 20 ns simulation. These results suggest that these TCM candidates could be potential FTO inhibitors through competitive inhibition.
引用
收藏
页码:471 / 483
页数:13
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