Epigallocatechin-3-gallate potently inhibits the in vitro activity of hydroxy-3-methyl-glutaryl-CoA reductase

被引:75
作者
Cuccioloni, Massimiliano [1 ]
Mozzicafreddo, Matteo [1 ]
Spina, Michele [1 ]
Chi Nhan Tran [1 ]
Falconi, Maurizio [1 ]
Eleuteri, Anna Maria [1 ]
Angeletti, Mauro [1 ]
机构
[1] Univ Camerino, Sch Biosci & Biotechnol, I-62032 Camerino, Italy
关键词
cholesterol; reduced nicotinamide adenine dinucleotide phosphate; epigallocatechin-3-gallate; inhibition; HMG-COA REDUCTASE; COENZYME-A REDUCTASE; GREEN TEA POLYPHENOL; ENOYL-ACP REDUCTASE; CARDIOVASCULAR-DISEASE; DIHYDROFOLATE-REDUCTASE; PLASMODIUM-FALCIPARUM; CHOLESTEROL-SYNTHESIS; PLASMA-CHOLESTEROL; METABOLIC SYNDROME;
D O I
10.1194/jlr.M011817
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydroxy-3-methyl-glutaryl-CoA reductase (HMGR) is the rate-controlling enzyme of cholesterol synthesis, and owing to its biological and pharmacological relevance, researchers have investigated several compounds capable of modulating its activity with the hope of developing new hypocholesterolemic drugs. In particular, polyphenol-rich extracts were extensively tested for their cholesterol-lowering effect as alternatives, or adjuvants, to the conventional statin therapies, but a full understanding of the mechanism of their action has yet to be reached. Our work reports on a detailed kinetic and equilibrium study on the modulation of HMGR by the most-abundant catechin in green tea, epigallocatechin- 3-gallate (EGCG).jlr Using a concerted approach involving spectrophotometric, optical biosensor, and chromatographic analyses, molecular docking, and site-directed mutagenesis on the cofactor site of HMGR, we have demonstrated that EGCG potently inhibits the in vitro activity of HMGR (K-i in the nanomolar range) by competitively binding to the cofactor site of the reductase. Finally, we evaluated the effect of combined EGCG-statin administration.-Cuccioloni, M., M. Mozzicafreddo, M. Spina, C. N. Tran, M. Falconi, A. M. Eleuteri, and M. Angeletti. Epigallocatechin-3-gallate potently inhibits the in vitro activity of hydroxy-3-methyl-glutaryl-CoA reductase. J. Lipid Res. 2011. 52: 897-907.
引用
收藏
页码:897 / 907
页数:11
相关论文
共 63 条
[1]   Green tea polyphenols: Novel and potent inhibitors of squalene epoxidase [J].
Abe, I ;
Seki, T ;
Umehara, K ;
Miyase, T ;
Noguchi, H ;
Sakakibara, J ;
Ono, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (03) :767-771
[2]  
ANGELIN B, 1984, J LIPID RES, V25, P1159
[3]   Epigallocatechin gallate is a slow-tight binding inhibitor of enoyl-ACP reductase from Plasmodium falciparum [J].
Banerjee, Tanushree ;
Sharma, Shailendra Kumar ;
Surolia, Namita ;
Surolia, Avadhesha .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 377 (04) :1238-1242
[4]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[5]   Prevalence and Progression of Subclinical Atherosclerosis in Younger Adults With Low Short-Term but High Lifetime Estimated Risk For Cardiovascular Disease The Coronary Artery Risk Development in Young Adults Study and Multi-Ethnic Study of Atherosclerosis [J].
Berry, Jarett D. ;
Liu, Kiang ;
Folsom, Aaron R. ;
Lewis, Cora E. ;
Carr, J. Jeffrey ;
Polak, Joseph F. ;
Shea, Steven ;
Sidney, Stephen ;
O'Leary, Daniel H. ;
Chan, Cheeling ;
Lloyd-Jones, Donald M. .
CIRCULATION, 2009, 119 (03) :382-389
[6]  
Bevington P. R., 2002, Data reduction and error analysis for the physical sciences
[7]  
Bieth J, 1974, SOME KINETIC CONSEQU
[8]   Prediction of binding constants of protein ligands: A fast method for the prioritization of hits obtained from de novo design or 3D database search programs [J].
Bohm, HJ .
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 1998, 12 (04) :309-323
[9]   THE COMPUTER-PROGRAM LUDI - A NEW METHOD FOR THE DENOVO DESIGN OF ENZYME-INHIBITORS [J].
BOHM, HJ .
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 1992, 6 (01) :61-78
[10]   The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice [J].
Bose, Mousumi ;
Lambert, Joshua D. ;
Ju, Jihyeung ;
Reuhl, Kenneth R. ;
Shapses, Sue A. ;
Yang, Chung S. .
JOURNAL OF NUTRITION, 2008, 138 (09) :1677-1683