Effects of a catechin-free fraction derived from green tea on gene expression of enzymes related to lipid metabolism in the mouse liver.

Many biological activities of green tea have been attributed to a major constituent, (minus;)-epigallocatechin gallate (EGCG). We previously reported that EGCG and an EGCG-free fraction derived from green tea modulated the gene expression of gluconeogenic enzymes, glucose-6-phosphatase and phosphoenolpyruvate carboxykinase, in the mouse liver. EGCG is also known to affect the gene expression of enzymes related to lipid metabolism. However, it remains to be examined whether or not a constituent other than EGCG contributes to the change in gene expression of these enzymes. In this study, we prepared an EGCG-free water-soluble fraction (GT-W), and examined its effects on the hepatic gene expression of lipogenic enzymes in mice. The results of quantitative real-time PCR assays indicated that the dietary administration of GT-W for 4 weeks reduced the hepatic gene expression of lipogenic enzymes: fatty acid synthase, hydroxymethylglutaryl coenzyme A reductase, and acetyl-coenzyme A carboxylase alpha. Also, the gene expression of sterol regulatory element-binding transcription factor (Srebf)1 and/or Srebf2 was reduced, suggesting that the reduction of Srebfs contributed to the down-regulation of the lipogenic enzymes, since these transcription factors bind the promoter region to enhance their expression. The plasma levels of triglycerides and cholesterol were reduced with statistical significance in the group given a diet containing GT-W. These results suggest that in addition to EGCG, green tea contains some component(s) which may help to prevent arteriosclerosis and obesity.

[1]  H. Tanabe,et al.  Effects of a catechin-free fraction derived from green tea on gene expression of gluconeogenic enzymes in rat hepatoma H4IIE cells and in the mouse liver. , 2011, Biomedical research.

[2]  H. Tanabe,et al.  Effects of catechin-rich green tea on gene expression of gluconeogenic enzymes in rat hepatoma H4IIE cells. , 2010, Biomedical research.

[3]  M. Jois,et al.  Green tea, black tea, and epigallocatechin modify body composition, improve glucose tolerance, and differentially alter metabolic gene expression in rats fed a high-fat diet. , 2009, Nutrition research.

[4]  Xin Wang,et al.  Cancer prevention by tea: animal studies, molecular mechanisms and human relevance , 2009, Nature Reviews Cancer.

[5]  Ji-Young Lee,et al.  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. , 2009, The Journal of nutrition.

[6]  H. Tanabe,et al.  Effects of chronic ingestion of catechin-rich green tea on hepatic gene expression of gluconeogenic enzymes in rats. , 2009, Biomedical research.

[7]  Jen-kun Lin,et al.  Epigallocatechin gallate (EGCG) attenuates high glucose-induced insulin signaling blockade in human hepG2 hepatoma cells. , 2008, Molecular nutrition & food research.

[8]  Takuji Suzuki,et al.  Differentiation-associated alteration in gene expression of importins and exportins in human leukemia HL-60 cells. , 2008, Biomedical research.

[9]  S. Wolfram Effects of Green Tea and EGCG on Cardiovascular and Metabolic Health , 2007, Journal of the American College of Nutrition.

[10]  Ying Wang,et al.  Epigallocatechin gallate supplementation alleviates diabetes in rodents. , 2006, The Journal of nutrition.

[11]  Reyes Artacho,et al.  Beneficial Effects of Green Tea—A Review , 2006, Journal of the American College of Nutrition.

[12]  C. Cho,et al.  Pharmacological effects of green tea on the gastrointestinal system. , 2004, European journal of pharmacology.

[13]  M. T. Travers,et al.  Induction of transcripts derived from promoter III of the acetyl-CoA carboxylase-alpha gene in mammary gland is associated with recruitment of SREBP-1 to a region of the proximal promoter defined by a DNase I hypersensitive site. , 2003, The Biochemical journal.

[14]  J. Inoue,et al.  Sterol Regulatory Element-binding Protein-2 Interacts with Hepatocyte Nuclear Factor-4 to Enhance Sterol Isomerase Gene Expression in Hepatocytes* , 2003, Journal of Biological Chemistry.

[15]  T. Murase,et al.  Beneficial effects of tea catechins on diet-induced obesity: stimulation of lipid catabolism in the liver , 2002, International Journal of Obesity.

[16]  D. Granner,et al.  Epigallocatechin Gallate, a Constituent of Green Tea, Represses Hepatic Glucose Production* , 2002, The Journal of Biological Chemistry.

[17]  T. Osborne,et al.  Sterol Regulatory Element-binding Proteins (SREBPs): Key Regulators of Nutritional Homeostasis and Insulin Action* , 2000, The Journal of Biological Chemistry.

[18]  M. Boschmann,et al.  The potential role of green tea catechins in the prevention of the metabolic syndrome - a review. , 2009, Phytochemistry.