Preclinical and clinical effects of Coleus forskohlii, Salacia reticulata and Sesamum indicum modifying pancreatic lipase inhibition in vitro and reducing total body fat

被引:16
作者
Badmaev, Vladimir [1 ]
Hatakeyama, Yoshitaka [2 ]
Yamazaki, Noriyuki [2 ]
Noro, Akira [2 ]
Mohamed, Faizal [3 ]
Ho, Chi-Tang [4 ]
Pan, Min-Hsiung [5 ,6 ,7 ]
机构
[1] Amer Med Holdings Inc, New York, NY 10314 USA
[2] New Drug Res Ctr Inc, Eniwa, Hokkaido, Japan
[3] Bio Act Japan KK, Tokyo, Japan
[4] Rutgers State Univ, Dept Food Sci, New Brunswick, NJ 08901 USA
[5] Natl Taiwan Univ, Inst Food Sci & Technol, Taipei 10617, Taiwan
[6] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung 40402, Taiwan
[7] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung, Taiwan
关键词
Coleus forskohlii; Salacia reticulata; Sesamum indicum; Pancreatic lipase; Body fat; EXTRACTS; DIET;
D O I
10.1016/j.jff.2015.03.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The herbal composition of Coleus forskohlii, Salacia reticulata, and Sesamum indicum, standardized for forskolin, mangiferin, and sesamin, respectively, were shown, in vitro, to inhibit pancreatic lipase with differing degrees and dynamics. In the placebo controlled six weeks clinical study the daily intake of 1000 mg C. forskohlii stand-alone standardized for 10% forskolin, showed statistically significant lowering of total body fat vs. baseline and placebo group (p <0.05). The computerized tomography showed decrease of total body fat and visceral fat in C.forskohlii group in comparison to the baseline. The potential of three herbal extracts preventing dietary fat absorption was emphasized by the in vitro synergy between C. forskohlii and S. reticulata inhibiting pancreatic lipase at higher rate than the fat-blocking activity generated by each component alone. The in vitro addition of S. indicum to the formula was found to synergistically assist inhibition of the pancreatic lipase in a lower dose range, while moderating the pancreatic lipase inhibition in a higher dose range. This dual mechanism of S. indicum was postulated as a safety mechanism preventing any potential side effects resulting from excessive inhibition of pancreatic lipase activity. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:44 / 51
页数:8
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