Literature DB >> 16506810

Modulation of cholesterol metabolism by the green tea polyphenol (-)-epigallocatechin gallate in cultured human liver (HepG2) cells.

Christina A Bursill1, Paul D Roach.   

Abstract

Epidemiological and animal studies have found that green tea is associated with lower plasma cholesterol. This study aimed to further elucidate how green tea modulates cholesterol metabolism. When HepG2 cells were incubated with the main green tea constituents, the catechins, epigallocatechin gallate (EGCG) was the only catechin to increase LDL receptor binding activity (3-fold) and protein (2.5-fold) above controls. EGCG increased the conversion of sterol regulatory element binding protein-1 (SREBP-1) to its active form (+56%) and lowered the cellular cholesterol concentration (-28%). At 50 microM, EGCG significantly lowered cellular cholesterol synthesis, explaining the reduction in cellular cholesterol. At 200 microM EGCG, cholesterol synthesis was significantly increased even though cellular cholesterol was lower, but there was a significant increase seen in medium cholesterol. This indicates that, at 200 microM, EGCG increases cellular cholesterol efflux. This study provides mechanisms by which green tea modulates cholesterol metabolism and indicates that EGCG might be its active constituent.

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Year:  2006        PMID: 16506810     DOI: 10.1021/jf051736o

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  20 in total

1.  Nanoencapsulation enhances epigallocatechin-3-gallate stability and its antiatherogenic bioactivities in macrophages.

Authors:  Jia Zhang; Shufang Nie; Shu Wang
Journal:  J Agric Food Chem       Date:  2013-09-10       Impact factor: 5.279

Review 2.  Role of the gut in modulating lipoprotein metabolism.

Authors:  Alan A Hennessy; R Paul Ross; Gerald F Fitzgerald; Noel Caplice; Catherine Stanton
Journal:  Curr Cardiol Rep       Date:  2014-08       Impact factor: 2.931

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

Authors:  Massimiliano Cuccioloni; Matteo Mozzicafreddo; Michele Spina; Chi Nhan Tran; Maurizio Falconi; Anna Maria Eleuteri; Mauro Angeletti
Journal:  J Lipid Res       Date:  2011-02-25       Impact factor: 5.922

4.  Hypolipidemic and antioxidant activity of the aqueous extract from the uneaten pulp of the fruit from Cordia dichotoma in healthy and hyperlipidemic Wistar albino rats.

Authors:  Samah A El-Newary; A M Sulieman; S R El-Attar; M Z Sitohy
Journal:  J Nat Med       Date:  2016-03-11       Impact factor: 2.343

5.  Progress of research in treatment of hyperlipidemia by monomer or compound recipe of Chinese herbal medicine.

Authors:  Xiao-bing Dou; Xing-de Wo; Chun-lei Fan
Journal:  Chin J Integr Med       Date:  2008-06-21       Impact factor: 1.978

6.  Green tea catechin EGCG inhibits ileal apical sodium bile acid transporter ASBT.

Authors:  Fadi Annaba; Pradeep Kumar; Amish K Dudeja; Seema Saksena; Ravinder K Gill; Waddah A Alrefai
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2010-01-07       Impact factor: 4.052

7.  GCG-rich tea catechins are effective in lowering cholesterol and triglyceride concentrations in hyperlipidemic rats.

Authors:  Sang Min Lee; Chae Wook Kim; Jung Kee Kim; Hyun Jung Shin; Joo Hyun Baik
Journal:  Lipids       Date:  2008-03-26       Impact factor: 1.880

8.  Green and black tea extracts inhibit HMG-CoA reductase and activate AMP kinase to decrease cholesterol synthesis in hepatoma cells.

Authors:  Dev K Singh; Subhashis Banerjee; Todd D Porter
Journal:  J Nutr Biochem       Date:  2008-10-15       Impact factor: 6.048

9.  A green tea catechin extract upregulates the hepatic low-density lipoprotein receptor in rats.

Authors:  Christina A Bursill; Paul D Roach
Journal:  Lipids       Date:  2007-06-21       Impact factor: 1.880

10.  Dietary green tea extract lowers plasma and hepatic triglycerides and decreases the expression of sterol regulatory element-binding protein-1c mRNA and its responsive genes in fructose-fed, ovariectomized rats.

Authors:  Sudeep Shrestha; Sarah J Ehlers; Ji-Young Lee; Maria-Luz Fernandez; Sung I Koo
Journal:  J Nutr       Date:  2009-02-04       Impact factor: 4.798

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