Abstract
Objective:
To examine in mice the acute effects of epigallocatechin gallate (EGCG), a green tea bioactive polyphenol on substrate metabolism with focus on the fate of dietary lipids.
Methods:
Male C57BL/6 mice were fed high-fat diets supplemented with EGCG extracted from green tea (TEAVIGO, DSM Nutritional Products Ltd, Basel, Switzerland) at different dosages up to 1% (w/w). Effects of EGCG on body composition (quantitative magnetic resonance), food intake and digestibility, oxidation and incorporation of exogenous lipids (stable isotope techniques: 13C-labeled palmitate and diet supplemented with corn oil as a natural source of 13C-enriched lipids) as well as gene expression (quantitative real-time PCR) in liver and intestinal mucosa were investigated.
Results:
Short-term supplementation (4–7 days) of dietary EGCG increased energy excretion, while food and energy intake were not affected. Fecal energy loss was accompanied by increased fat and nitrogen excretion. EGCG decreased post-prandial triglyceride and glycogen content in liver, increased oxidation of dietary lipids and decreased incorporation of dietary 13C-enriched lipids into fat tissues, liver and skeletal muscle. EGCG dose dependently reversed high-fat diet-induced effects on intestinal substrate transporters (CD36, FATP4 and SGLT1) and downregulated lipogenesis-related genes (ACC, FAS and SCD1) in liver in the post-prandial state.
Conclusions:
Anti-obesity effects of EGCG can be explained by a decreased food digestibility affecting substrate metabolism of intestinal mucosa and liver, leading to increased post-prandial fat oxidation and reduced incorporation of dietary lipids into tissues.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Wolf A, Bray GA, Popkin BM . A short history of beverages and how our body treats them. Obes Rev 2008; 9: 151–164.
Cabrera C, Artacho R, Giménez R . Beneficial effects of green tea--a review. J Am Coll Nutr 2006; 25: 79–99.
Khan N, Mukhtar H . Tea polyphenols for health promotion. Life Sci 2007; 81: 519–533.
Chen D, Milacic V, Chen MS, Wan SB, Lam WH, Huo C et al. Tea polyphenols, their biological effects and potential molecular targets. Histol Histopathol 2008; 23: 487–496.
Thielecke F, Boschmann M . The potential role of green tea catechins in the prevention of the metabolic syndrome - a review. Phytochemistry 2009; 70: 11–24.
Wolfram S, Wang Y, Thielecke F . Anti-obesity effects of green tea: from bedside to bench. Mol Nutr Food Res 2006; 50: 176–187.
Grove KA, Lambert JD . Laboratory, epidemiological, and human intervention studies show that tea (Camellia sinensis) may be useful in the prevention of obesity. J Nutr 2010; 140: 446–453.
Dulloo AG, Duret C, Rohrer D, Girardier L, Mensi N, Fathi M et al. Efficacy of a green tea extract rich in catechin polyphenols and caffeine in increasing 24-h energy expenditure and fat oxidation in humans. Am J Clin Nutr 1999; 70: 1040–1045.
Choo JJ . Green tea reduces body fat accretion caused by high-fat diet in rats through beta-adrenoceptor activation of thermogenesis in brown adipose tissue. J Nutr Biochem 2003; 14: 671–676.
Klaus S, Pültz S, Thone-Reineke C, Wolfram S . Epigallocatechin gallate attenuates diet-induced obesity in mice by decreasing energy absorption and increasing fat oxidation. Int J Obes (Lond) 2005; 29: 615–623.
Wolfram S . Effects of green tea and EGCG on cardiovascular and metabolic health. J Am Coll Nutr 2007; 26: 373S–388S.
Bose M, Lambert JD, Ju J, Reuhl KR, Shapses SA, Yang CS . The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice. J Nutr 2008; 138: 1677–1683.
Lee MS, Kim CT, Kim Y . Green tea (-)-epigallocatechin-3-gallate reduces body weight with regulation of multiple genes expression in adipose tissue of diet-induced obese mice. Ann Nutr Metab 2009; 54: 151–157.
Raederstorff DG, Schlachter MF, Elste V, Weber P . Effect of EGCG on lipid absorption and plasma lipid levels in rats. J Nutr Biochem 2003; 14: 326–332.
Boschmann M, Thielecke F . The effects of epigallocatechin-3-gallate on thermogenesis and fat oxidation in obese men: a pilot study. J Am Coll Nutr 2007; 26: 389S–395S.
Thielecke F, Rahn G, Böhnke J, Adams F, Birkenfeld AL, Jordan J et al. Epigallocatechin-3-gallate and postprandial fat oxidation in overweight/obese male volunteers: a pilot study. Eur J Clin Nutr 2010; 64: 704–713.
Donovan JL, Crespy V, Manach C, Morand C, Besson C, Scalbert A et al. Catechin is metabolized by both the small intestine and liver of rats. J Nutr 2001; 131: 1753–1757.
Hwang JT, Park IJ, Shin JI, Lee YK, Lee SK, Baik HW et al. Genistein, EGCG, and capsaicin inhibit adipocyte differentiation process via activating AMP-activated protein kinase. Biochem Biophys Res Commun 2005; 338: 694–699.
Moon HS, Chung CS, Lee HG, Kim TG, Choi YJ, Cho CS . Inhibitory effect of (-)-epigallocatechin-3-gallate on lipid accumulation of 3T3-L1 cells. Obesity (Silver Spring) 2007; 15: 2571–2582.
Sakurai N, Mochizuki K, Kameji H, Shimada M, Goda T . Epigallocatechin gallate enhances the expression of genes related to insulin sensitivity and adipocyte differentiation in 3T3-L1 adipocytes at an early stage of differentiation. Nutrition 2009; 25: 1047–1056.
Kim H, Hiraishi A, Tsuchiya K, Sakamoto K . Epigallocatechin gallate suppresses the differentiation of 3T3-L1 preadipocytes through transcription factors FoxO1 and SREBP1c. Cytotechnology 2010; 62: 245–255.
Klaus S . Increasing the protein:carbohydrate ratio in a high-fat diet delays the development of adiposity and improves glucose homeostasis in mice. J Nutr 2005; 135: 1854–1858.
Petzke KJ, Boeing H, Klaus S, Metges CC . Carbon and nitrogen stable isotopic composition of hair protein and amino acids can be used as biomarkers for animal-derived dietary protein intake in humans. J Nutr 2005; 135: 1515–1520.
Isken F, Klaus S, Petzke KJ, Loddenkemper C, Pfeiffer AF, Weickert MO . Impairment of fat oxidation under high- vs low-glycemic index diet occurs before the development of an obese phenotype. Am J Physiol Endocrinol Metab 2010; 298: E287–E295.
Fernandez-Quintela A, Churruca I, Portillo MP . The role of dietary fat in adipose tissue metabolism. Public Health Nutr 2007; 10: 1126–1131.
Petzke KJ, Klaus S . Reduced postprandial energy expenditure and increased exogenous fat oxidation in young woman after ingestion of test meals with a low protein content. Nutr Metab (Lond) 2008; 5: 25.
Katterle Y, Keipert S, Hof J, Klaus S . Dissociation of obesity and insulin resistance in transgenic mice with skeletal muscle expression of uncoupling protein 1. Physiol Genomics 2008; 32: 352–359.
Noatsch A, Petzke KJ, Millrose MK, Klaus S . Body weight and energy homeostasis was not affected in C57BL/6 mice fed high whey protein or leucine-supplemented low-fat diets. Eur J Nutr 2010; e-pub ahead of print 18 December 2010; doi:10.1007/s00394-010-0155-2.
Park HJ, Dinatale DA, Chung MY, Park YK, Lee JY, Koo SI et al. Green tea extract attenuates hepatic steatosis by decreasing adipose lipogenesis and enhancing hepatic antioxidant defenses in ob/ob mice. J Nutr Biochem 2011; 22: 393–400.
Lonac MC, Richards JC, Schweder MM, Johnson TK, Bell C . Influence of short term consumption of the caffeine free, epigallocatechin 3 gallate supplement, Teavigo, on resting metabolism and the thermic effect of feeding. Obesity 2011; 19: 298–304.
Unno T, Osada C, Motoo Y, Suzuki Y, Kobayashi M, Nozawa A . Dietary tea catechins increase fecal energy in rats. J Nutr Sci Vitaminol (Tokyo) 2009; 55: 447–451.
Shimizu M, Kobayashi Y, Suzuki M, Satsu H, Miyamoto Y . Regulation of intestinal glucose transport by tea catechins. Biofactors 2000; 13: 61–65.
Papadopoulou A, Frazier RA . Characterization of protein-polyphenol interactions. Trends Food Sci Technol 2004; 15: 186–190.
Tadera K, Minami Y, Takamatsu K, Matsuoka T . Inhibition of alpha-glucosidase and alpha-amylase by flavonoids. J Nutr Sci Vitaminol (Tokyo) 2006; 52: 149–153.
Juhel C, Armand M, Pafumi Y, Rosier C, Vandermander J, Lairon D . Green tea extract (AR25) inhibits lipolysis of triglycerides in gastric and duodenal medium in vitro. J Nutr Biochem 2000; 11: 45–51.
Ohnishi R, Iga K, Kiriyama S . Green tea polyphenols reduce protein digestibility and suppress cecal fermentation in rats. J Jpn Soc Nutr Food Sci 2005; 58: 199–208.
Hara Y, Honda M . Inhibition of alpha-amylase by tea polyphenols. Agric Biol Chem 1990; 54: 1939–1945.
Murase T, Nagasawa A, Suzuki J, Hase T, Tokimitsu I . Beneficial effects of tea catechins on diet-induced obesity: stimulation of lipid catabolism in the liver. Int J Obes Relat Metab Disord 2002; 26: 1459–1464.
Murase T, Misawa K, Haramizu S, Hase T . Catechin-induced activation of the LKB1/AMP-activated protein kinase pathway. Biochem Pharmacol 2009; 78: 78–84.
Suzuki Y, Unno T, Kobayashi M, Nozawa A, Sagesaka Y, Kakuda T . Dose-dependent suppression of tea catechins with a galloyl moiety on postprandial hypertriglyceridemia in rats. Biosci Biotechnol Biochem 2005; 69: 1288–1291.
Ikeda I, Tsuda K, Suzuki Y, Kobayashi M, Unno T, Tomoyori H et al. Tea catechins with a galloyl moiety suppress postprandial hypertriacylglycerolemia by delaying lymphatic transport of dietary fat in rats. J Nutr 2005; 135: 155–159.
Shimomura Y, Tamura T, Suzuki M . Less body fat accumulation in rats fed a safflower oil diet than in rats fed a beef tallow diet. J Nutr 1990; 120: 1291–1296.
Dulloo AG, Mensi N, Seydoux J, Girardier L . Differential effects of high-fat diets varying in fatty acid composition on the efficiency of lean and fat tissue deposition during weight recovery after low food intake. Metabolism 1995; 44: 273–279.
Flint A, Helt B, Raben A, Toubro S, Astrup A . Effects of different dietary fat types on postprandial appetite and energy expenditure. Obes Res 2003; 11: 1449–1455.
Acknowledgements
We are grateful to Antje Sylvester, Karin Schaller, Elke Thom, and Elisabeth Meyer for excellent technical assistance. SK is a member of EU COST action MITOFOOD (FA0602). This study was supported by DSM Nutritional Products, Human Nutrition and Health, Basel, Switzerland.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
Dr Raederstorff and Dr Wolfram are employees of DSM Nutritional Products Ltd, which also provided TEAVIGO and research funding to Dr Klaus. Dr Friedrich and Dr Petzke declare no potential conflict of interest.
Additional information
Supplementary Information accompanies the paper on International Journal of Obesity website
Supplementary information
Rights and permissions
About this article
Cite this article
Friedrich, M., Petzke, K., Raederstorff, D. et al. Acute effects of epigallocatechin gallate from green tea on oxidation and tissue incorporation of dietary lipids in mice fed a high-fat diet. Int J Obes 36, 735–743 (2012). https://doi.org/10.1038/ijo.2011.136
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/ijo.2011.136
Keywords
This article is cited by
-
High-fat diet accelerate hepatic fatty acids synthesis in offspring male rats induced by perinatal exposure to nonylphenol
BMC Pharmacology and Toxicology (2021)
-
Extended indirect calorimetry with isotopic CO2 sensors for prolonged and continuous quantification of exogenous vs. total substrate oxidation in mice
Scientific Reports (2019)
-
Effect of Epigallo-Catechin-3-Gallate on Lipid Metabolism Related Gene Expression and Yolk Fatty Acid Profiles of Laying Hens Exposed to Vanadium
Biological Trace Element Research (2019)
-
Neurobehavioral changes in mice offspring exposed to green tea during fetal and early postnatal development
Behavioral and Brain Functions (2017)
-
Daily ingestion of catechin-rich beverage increases brown adipose tissue density and decreases extramyocellular lipids in healthy young women
SpringerPlus (2016)