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Inhibitory Activity of Diacylglycerol Acyltransferase by Tanshinones from the Root of Salvia miltiorrhiza  

Ko, Jeong-Suk (Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology)
Ryu, Shi-Young (Korea Research Institute of Chemical Technology)
Kim, Young-Sup (Korea Research Institute of Chemical Technology)
Chung, Mi-Yeon (Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology)
Kang, Jong-Seong (College of Pharmacy, Chungnam National University)
Rho, Mun-Chual (Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology)
Lee, Hyun-Sun (Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology)
Kim, Young-Kook (Cardiovascular Research Laboratory, Korea Research Institute of Bioscience and Biotechnology)
Publication Information
Archives of Pharmacal Research / v.25, no.4, 2002 , pp. 446-448 More about this Journal
Abstract
The inhibitory activity of tanshinones from Salvia miltiorrhiza was tested on rat liver diacylglycerol acyltransferase (DGAT). Cryptotanshinone (1) and 15,16-dihydrotanshinone I (3) exhibited potent DGAT inhibitory activities dose-dependently with $IC_{50}$ values of $10.5 {\;}{\mu\textrm{g}}/ml{\;}and{\;}11.1{\;}{\mu\textrm{g}}/ml$. However, tanshinone IIA (2) and tanshinone I (4) showed very weak inhibition ($IC_{50}{\;}value:{\;}>{\;}250{\;}{\mu\textrm{g}}/ml$). A dihydrofuran moiety was seemed to be responsible for the stronger inhibitory activity
Keywords
Salvia miltiorrhiza; Labiatae; Tanshinones; Diacylglycerol acyltransferase;
Citations & Related Records

Times Cited By Web Of Science : 20  (Related Records In Web of Science)
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1 Lehner R, Kuksis A., Biosynthesis of triacylglycerols. Prog. Lipid Res., 35, 169-201 (1996)   DOI   ScienceOn
2 Ryu, S. Y., Lee, C. O., and Choi, S. U., In vitro cytotoxicity of tanshinones from Salvia miltiorrhiza. Planta Med., 63, 339-342 (1997)   DOI   ScienceOn
3 Tabata N, Ito M, Tomoda H, Omura S. Xanthohumols, diacylglycerol acyltransferase inhibitors, from Humulus lupulus. Phytochemistry, 46, 683-687 (1997)   DOI   ScienceOn
4 Chang, H., and But, P. (Eds). Pharmacology and Applications of Chinese Materia Medica; World Scientific Publishing Co., Singapore, pp. 255-268 (1986)
5 Coleman RA. Diacylglycerol acyltransferase and monoacylglycerol acyltransferase from liver and intestine. Methods Enzymol., 209, 98-103 (1992)   DOI   PUBMED
6 Smith SJ, Cases S, Jensen DR, Chen HC, Sande E, Tow Bryan, Sanan DA, Rober J, Eckel RH, Farese Jr RV. Obesity resistance and multiple mechanisms of triglyceride synthesis in mice lacking Dgat. Nat. Genet., 25, 87-90 (2000)   DOI   ScienceOn
7 Cases S, Smith S, Zheng Y, Myers H, Lear SR., Sande E, Novak S, Collins C, Welch B, Lusis AJ, Erickson SK, Farese Jr RV. Identification of a gene encoding an acyl CoA:diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis. Proc. Natl. Acad. Sci. USA, 95, 13018-13023 (1998)   DOI   ScienceOn
8 Gray GA, Tartaglia LA. Medicinal strategies in the treatment of obesity. Curr. Opin. Lipidol., 11, 229-234 (2000)   DOI   ScienceOn
9 Tomoda H, Ito M, Tabata N, Masuma R, Yamaguchi Y, Omura S. Amidepsines, inhibitors of diacylglycerol acyltransferase produced by Humicola sp. FO-2942. J. Antibiotics, 48, 937-941(1995)   DOI
10 Tomoda H, Ohyama Y., Abe T, Tabata N, Namikoshi M, Yamaguchi Y, Masuma R, Omura S. Roselipines, inhibitors of diacylglycerol acyltransferase, produced by Gliocalidum roseum KF-1040. J. Antibiotics, 52, 689-694 (1999)   DOI