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3/2017 vol. 67
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Effect of Green Tea Extract-Enriched Diets on Insulin and Leptin Levels, Oxidative Stress Parameters and Antioxidant Enzymes Activities in Obese Mice
Hana Bártíková
,
 
Iva Boušová
,
 
Petra Matoušková
,
 
Barbora Szotáková
,
 
Lenka Skálová
 
 
 
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Publication date: 2017-09-30
 
 
Pol. J. Food Nutr. Sci. 2017;67(3):233-240
DOI: https://doi.org/10.1515/pjfns-2017-0004
 
 
Article (PDF)
References (41) Citations (6)
 
KEYWORDS
monosodium glutamate induced obesity
catechins
Oxidative stress
polyphenon 60
 
ABSTRACT
Green tea and green tea extracts (GTE) are often incorporated into diet intended to weight reduction, although the information about their efficacy in obese individuals is insufficient. The present study was designed to follow up the effect of defined and standardized GTE in mice with obesity induced by monosodium L-glutamate. Obese mice were fed with GTE-supplemented diet in three dosage regimens: 28-day and 3-day intake of 1 g GTE in 1 kg of diet and 28-day intake of 0.1 g GTE in 1 kg of diet. The information on body weight, food intake, oxidation stress parameters in blood and antioxidant enzymes activity in liver and small intestine was obtained. High doses of GTE decreased the specific activities of glutathione reductase and catalase and increase concentrations of malondialdehyde in blood. Specific activities of antioxidant enzymes in the liver and small intestine were not altered after GTE treatment except the decrease of NAD(P)H:quinone oxidoreductase activity. Our results showed that GTE did not affect average body weight and did not markedly improve antioxidant status in glutamate-induced obese mice. Moreover, intake of high doses of GTE made antioxidant defense in obese animals even worse.
 
REFERENCES (41)
1.
Afrin S., Gasparrini M., Forbes-Hernandez T.Y., Reboredo-Rodriguez P., Mezzetti B., Varela-Lopez A., Giampieri F., Battino M., Promising health benefits of the strawberry: A focus on clinical studies. J. Agric. Food Chem., 2016, 64, 4435-4449.
Google Scholar
 
 
2.
Akaberi M., Hosseinzadeh H., Grapes (Vitis vinifera) as a potential candidate for the therapy of the metabolic syndrome. Phytotherap. Res., 2016, 30, 540-556.
Google Scholar
 
 
3.
Alarcon-Aguilar F.J., Zamilpa A., Perez-Garcia M.D., Almanza-Perez J.C., Romero-Nunez E., Campos-Sepulveda E.A., Vazquez-Carrillo L.I., Roman-Ramos R., Effect of Hibiscus sabdariffa on obesity in MSG mice. J. Ethnopharmacol., 2007, 114, 66-71.
Google Scholar
 
 
4.
Amiot M.J., Riva C., Vinet A., Effects of dietary polyphenols on metabolic syndrome features in humans: a systematic review. Obesity Rev., 2016, 17, 573-586.
Google Scholar
 
 
5.
Bartikova H., Skalova L., Valentova K., Matouskova P., Szotakova B., Martin J., Kvita V., Bousova I., Effect of oral administration of green tea extract in various dosage schemes on oxidative stress status of mice in vivo. Acta Pharm., 2015, 65, 65-73.
Google Scholar
 
 
6.
Boušová I., Matoušková P., Bártíková H., Szotáková B. Hanušová V., Tománková V., Anzenbacherová E., Lišková B., Anzenbacher P., Skálová L., Influence of diet supplementation with green tea extract on drug-metabolizing enzymes in a mouse model of monosodium glutamate-induced obesity. Eur. J. Nutr., 2016, 55, 361-371.
Google Scholar
 
 
7.
Cullen J.J., Hinkhouse M.M., Grady M., Gaut A.W., Liu J., Zhang Y.P., Weydert C.J., Domann F.E., Oberley L.W., Dicumarol inhibition of NADPH:quinone oxidoreductase induces growth inhibition of pancreatic cancer via a superoxide-mediated mechanism. Cancer Res, 2003, 63, 5513-5520.
Google Scholar
 
 
8.
Del Rio D., Stewart A.J., Pellegrini N., A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutr Metab Cardiovasc Dis, 2005, 15, 316-328.
Google Scholar
 
 
9.
Fitzsimmons S.A., Workman P., Grever M., Paull K., Camalier R., Lewis A.D., Reductase enzyme expression across the National Cancer Institute Tumor cell line panel: correlation with sensitivity to mitomycin C and EO9. J Natl Cancer Inst, 1996, 88, 259-269.
Google Scholar
 
 
10.
Flohé L., Günzler W.A., Assays of glutathione peroxidase. Methods Enzymol, 1984, 105, 114-121.
Google Scholar
 
 
11.
Fujimoto M., Tsuneyama K., Fujimoto T., Selmi C., Gershwin M.E., Shimada Y., Spirulina improves non-alcoholic steatohepatitis, visceral fat macrophage aggregation, and serum leptin in a mouse model of metabolic syndrome. Dig Liver Dis, 2012a, 44, 767-774.
Google Scholar
 
 
12.
Fujimoto M., Tsuneyama K., Chen S.Y., Nishida T., Chen J.L., Chen Y.C., Fujimoto T., Imura J., Shimada Y., Study of the effects of monacolin k and other constituents of red yeast rice on obesity, insulin-resistance, hyperlipidemia, and nonalcoholic steatohepatitis using a mouse model of metabolic syndrome. Evid Based Complement Alternat Med, 2012b, 892697,.
Google Scholar
 
 
13.
Góth L., A simple method for determination of serum catalase activity and revision of reference range. Clin Chim Acta, 1991, 196, 143-151,.
Google Scholar
 
 
14.
Habig W.H., Pabst M.J., Jakoby W.B., Glutathione S-Transferases: The first enzymatic step in mercapturic acid formation. J Biol Chem, 1974, 249, 7130-7139,.
Google Scholar
 
 
15.
Handy D.E., Lubos E., Yang Y., Galbraith J.D., Kelly N., Zhang Y.Y., Leopold J.A., Loscalzo J., Glutathione peroxidase-1 regulates mitochondrial function to modulate redox-dependent cellular responses. J Biol Chem, 2009, 284, 11913-11921.
Google Scholar
 
 
16.
Henning S.M., Fajardo-Lira C., Lee H.W., Youssefian A.A., Go V.L., Heber D., Catechin content of 18 teas and a green tea extract supplement correlates with the antioxidant capacity. Nutr Cancer, 2003, 45, 226-235. missing in the text.
Google Scholar
 
 
17.
Chacko S.M., Thambi P.T., Kuttan R., Nishigaki I., Beneficial effects of green tea: a literature review. Chin Med, 2010, 5, 13.please move before Cullen acc. to alphabetical order.
Google Scholar
 
 
18.
Johnson R., Bryant S., Huntley A.L., Green tea and green tea catechin extracts: an overview of the clinical evidence. Maturitas, 2012, 73, 280-287,.
Google Scholar
 
 
19.
Khan N., Afaq F., Saleem M., Ahmad N., Mukhtar H., Targeting multiple signaling pathways by green tea polyphenol (-)-epigallocatechin-3-gallate. Cancer Res, 2006, 66, 2500-2505,.
Google Scholar
 
 
20.
Khan S.A., Priyamvada S., Arivarasu N.A., Khan S., Yusufi A.N., Influence of green tea on enzymes of carbohydrate metabolism, antioxidant defense, and plasma membrane in rat tissues. Nutrition, 2007, 23, 687-695,.
Google Scholar
 
 
21.
Khan S.G., Katiyar S.K., Agarwal R., Mukhtar H., Enhancement of antioxidant and phase II enzymes by oral feeding of green tea polyphenols in drinking water to SKH-1 hairless mice: possible role in cancer chemoprevention. Cancer Res, 1992, 52, 4050-4052,.
Google Scholar
 
 
22.
Lambert J.D., Lee M.J., Diamond L., Ju J., Hong J., Bose M., Newmark H.L., Yang C.S., Dose-dependent levels of epigallocatechin-3-gallate in human colon cancer cells and mouse plasma and tissues. Drug Metab Dispos, 2006, 34, 8-11,.
Google Scholar
 
 
23.
Lambert J.D., Lee M.J., Lu H., Meng X., Hong J.J., Seril D.N., Sturgill M.G., Yang C.S., Epigallocatechin-3-gallate is absorbed but extensively glucuronidated following oral administration to mice. J Nutr, 2003, 133, 4172-4177,.
Google Scholar
 
 
24.
Lin Y.L., Cheng C.Y., Lin Y.P., Lau Y.W., Juan I.M., Lin J.K., Hypolipidemic effect of green tea leaves through induction of antioxidant and phase II enzymes including superoxide dismutase, catalase, and glutathione S-transferase in rats. J Agric Food Chem, 1998, 46, 1893-1899,.
Google Scholar
 
 
25.
Martin M.A., Serrano A.B., Ramos S., Pulido M.I., Bravo L., Goya L., Cocoa flavonoids up-regulate antioxidant enzyme activity via the ERK1/2 pathway to protect against oxidative stress-induced apoptosis in HepG2 cells. J Nutr Biochem, 2010, 21, 196-205,.
Google Scholar
 
 
26.
Matouskova P., Bartikova H., Bousova I., Levorova L., Szotakova B., Skalova L., Drug-metabolizing and antioxidant enzymes in monosodium L-glutamate obese mice. Drug Metab Dispos, 2015, 43, 258-265,.
Google Scholar
 
 
27.
Matouskova P., Bartikova H., Bousova I., Szotakova B., Martin J., Skorkovska J., Hanusova V., Tomankova V., Anzenbacherova E., Liskova B., Anzenbacher P., Skalova L., Effect of defined green tea extract in various dosage schemes on drug-metabolizing enzymes in mice in vivo. J Funct Foods, 2014, 10, 327-335,.
Google Scholar
 
 
28.
Matyskova R., Maletinska L., Maixnerova J., Pirnik Z., Kiss A., Zelezna B., Comparison of the obesity phenotypes related to monosodium glutamate effect on arcuate nucleus and/or the high fat diet feeding in C57BL/6 and NMRI mice. Physiol Res, 2008, 57, 727-734.
Google Scholar
 
 
29.
Murakami A., Dose-dependent functionality and toxicity of green tea polyphenols in experimental rodents. Arch Biochem Biophys, 2014, 557, 3-10.
Google Scholar
 
 
30.
Na H.K., Surh Y.J., Modulation of Nrf2-mediated antioxidant and detoxifying enzyme induction by the green tea polyphenol EGCG. Food Chem Toxicol, 2008, 46, 1271-1278,.
Google Scholar
 
 
31.
Noeman S.A., Hamooda H.E., Baalash A.A., Biochemical study of oxidative stress markers in the liver, kidney and heart of high fat diet induced obesity in rats. Diabetol Metab Syndr, 2011, 3, 17-22,.
Google Scholar
 
 
32.
Olney J.W., Brain lesions, obesity, and other disturbances in mice treated with monosodium glutamate. Science, 1969, 164, 719-721,.
Google Scholar
 
 
33.
Osei-Hyiaman D., Liu J., Zhou L., Godlewski G., Harvey-White J., Jeong W.I., Batkai S., Marsicano G., Lutz B., Buettner C., Kunos G., Hepatic CB(1) receptor is required for development of diet-induced steatosis, dyslipidemia, and insulin and leptin resistance in mice. J Clin Invest, 2008, 118, 3160-3169.
Google Scholar
 
 
34.
Park H.J., DiNatale D.A., Chung M.Y., Park Y.K., Lee J.Y., Koo S.I., O'Connor M., Manautou J.E., Bruno R.S., 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,.
Google Scholar
 
 
35.
Picklo M., Claycombe K.J., Meydani M., Adipose Dysfunction, Interaction of Reactive Oxygen Species, and Inflammation. Adv Nutr, 2012, 3, 734-735,.
Google Scholar
 
 
36.
Ramesh E., Elanchezhian R., Sakthivel M., Jayakumar T., Senthil Kumar R.S., Geraldine P., Thomas P.A., Epigallocatechin gallate improves serum lipid profile and erythrocyte and cardiac tissue antioxidant parameters in Wistar rats fed an atherogenic diet. Fundam Clin Pharmacol, 2008, 22, 275-284.
Google Scholar
 
 
37.
Savini I., Catani M.V., Evangelista D., Gasperi V., Avigliano L., Obesity-associated oxidative stress: strategies finalized to improve redox state. Int J Mol Sci, 2013, 14, 10497-10538.
Google Scholar
 
 
38.
Seeley S.K., Poposki J.A., Maksimchuk J., Tebbe J., Gaudreau J., Mannervik B., Bull A.W., Metabolism of oxidized linoleic acid by glutathione transferases: peroxidase activity toward 13-hydroperoxyoctadecadienoic acid. Biochim Biophys Acta, 2006, 1760, 1064-1070,.
Google Scholar
 
 
39.
Tomankova V., Liskova B., Skalova L., Bartikova H., Bousova I., Jourova L., Anzenbacher P., Ulrichova J., Anzenbacherova E., Altered cytochrome P450 activities and expression levels in the liver and intestines of the monosodium glutamate-induced mouse model of human obesity. Life Sci, 2015, 133, 15-20.
Google Scholar
 
 
40.
Wang Y., Chun O.K., Song W.O., Plasma and Dietary Antioxidant Status as Cardiovascular Disease Risk Factors: A Review of Human Studies. Nutrients, 2013, 5, 2969-3004,.
Google Scholar
 
 
41.
Wiegand H., Boesch-Saadatmandi C., Regos I., Treutter D., Wolffram S., Rimbach G., Effects of quercetin and catechin on hepatic glutathione-S transferase (GST), NAD(P)H quinone oxidoreductase 1 (NQO1), and antioxidant enzyme activity levels in rats. Nutr Cancer, 2009, 61, 717-722.
Google Scholar
 
 
 
CITATIONS (6):
1.
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