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http://dx.doi.org/10.3746/jkfn.2010.39.3.350

Protective Effect of Theanine on the Acetaminophen-induced Hepatotoxicity  

Eu, Jung-Bu (School of Food Science International University of Korea)
Kim, Sun-Oh (Jeonnam Natural Resources Research Institute)
Seoung, Tae-Jong (School of Food Science International University of Korea)
Choi, Sung-Gil (Division of Applied Life Sciences, Graduate School, Institute of Agricultural & Agricultural & Life Sciences, Gyeongsang National University)
Cho, Sung-Hwaon (Division of Applied Life Sciences, Graduate School, Institute of Agricultural & Agricultural & Life Sciences, Gyeongsang National University)
Choi, Chul-Yung (Dept. of Pharmaceutical Formulation Engineering, International University of Korea)
Publication Information
Journal of the Korean Society of Food Science and Nutrition / v.39, no.3, 2010 , pp. 350-355 More about this Journal
Abstract
The hepatoprotective effects of theanine on acetaminophen (APAP)-induced hepatotoxicity were investigated in vivo and in vitro. The effects of theanine on liver toxicity induced by APAP were assessed by blood biochemical and histopathological analyses. APAP treatment (400 mg/kg) caused severe liver injury in mice as indicated by their significantly elevated plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Pretreatment with theanine for 3 days attenuated the increase in ALT and AST when challenged with APAP. These protective effects of theanine against APAP-induced toxicity were consistent with the results from the histopathological examinations. We next examined the effects of theanine on the GSH concentration in liver plasma. The hepatic GSH level was significantly elevated in a dose-dependent manner by theanine treatment. The results suggest that the protective effects of theanine APAP-induced hapatotoxicity by antioxidative effect and GSH induction, implying that theanine should be considered a potential chemopreventive agent.
Keywords
theanine; MDA; GSH; acetaminophen; hepatoprotection;
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1 Goto T, Yoshida Y, Amano I, Horie H. 1996. Simultaneous analysis of individual catechins and caffeine in green tea. Foods & Food Ingred J Jpn 170: 46-51.
2 Graham HN. 1992. Green tea composition, consumption, and polyphenol chemistry. Prev Med 21: 334-350.   DOI
3 Hasegawa R, Chujo T. 1995. Preventive effects of green tea against liver oxidative DNA damage and hepatotoxicity in rate treated with 2-nitropane. Food Chem Toxicol 33: 961-970.   DOI
4 Ashihara H, Sano H, Crozier A. 2008. Caffeine and related purine alkaloids: biosynthesis, catabolism, function and genetic engineering. Phytochemistry 69: 841-856.   DOI
5 Imaeda AB, Watanabe A, Sohail MA, Mahmood S, Mohamadnejad M, Sutterwala FS, Flavell RA, Mehal WZ. 2009. Acetaminophen-induced hepatotoxicity in mice is dependent on Tlr9 and the Nalp3 inflammasome. J Clin Invest 119: 305-314.
6 Lee WM. 2004. Acetaminophen and the US Acute Liver Failure Study Group: lowering the risks of hepatic failure. Hepatology 40: 6-9.   DOI
7 Laine JE, Auriola S, Pasanen M, Juvonen RO. 2009. Acetaminophen bioactivation by human cytochrome P450 enzymes and animal microsomes. Xenobiotica 39: 11-21.   DOI
8 Fischer LJ, Green MD, Harman AW. 1986. Levels of acetaminophen and its metabolites in mouse tissue after a toxic dose. J Pharmacol EXP Ther 219: 281-286.
9 Shim CK. 2004. Implementation and policy direction of the Korean health functional food law and its regulations. Food Sci Ind 37: 37-40.
10 Kim HK. 2004. Current status and prospect of nutraceuticals. Food Ind Nutr 9: 1-14.   과학기술학회마을
11 Matsuzaki T, Hata Y. 1985. Antioxidative activity of tea leaf catechins. Nippon Nogeikagaku Kaish 59: 129-134.   DOI
12 Wang EJ, Li Y, Lin M, Chen L, Stein A, Reuhl KR, Yang CS. 1996. Protective effects of garlic and related organosulfur compounds on acetaminophen-induced hepatotoxicity in mice. Toxicol Appl Pharmacol 136: 146-154.   DOI
13 Wu YL, Piao DM, Han XH, Nan JX. 2008. Protective effects of salidroside against acetaminophen-induced toxicity in mice. Biol Pharm Bull 31: 1523-1529.   DOI
14 Friedman M, Mackey BE, Kim HJ, Lee IS, Lee KR, Lee SU, Kozukue E, Kozukue N. 2007. Structure-activity relationships of tea compounds against human cancer cells. J Agric Food Chem 24: 243-253.
15 Casimir J, Jadot J, Renard M. 1960. Separation and characterization of N-ethyl-$\gamma$-glutamine from Xerocomus badius. Biochim Biophys Acta 39: 462-468.   DOI
16 Guengerich FP, Kim DH, Iwasaki M. 1991. Role of human cytochrome P-450 IIEL in the oxidation of many low molecular weight cancer suspects. Chem Res Toxicol 4: 168-179.   DOI
17 Crozier A, Yokota T, Jaganath IB, Marks SC, Saltmarsh M, Clifford MN. 2006. Secondary metabolites in fruits, vegetables, beverages and other plant-based dietary components. In Plant Secondary Metabolites. Blackwell, Oxford, England. Chapter 7, p 208-302.
18 Sakato A. 1949. The chemical constituents of tea. III. A new amide theanine. Nippon Nogeikagaku Kaishi 23: 262-267.
19 Pacheco GS, Panatto JP, Fagundes DA, Scaini G, Bassani C, Jeremias IC, Rezin GT, Constantino L, Dal-Pizzol F, Streck EL. 2009. Brain creatine kinase activity is inhibited after hepatic failure induced by carbon tetrachloride or acetaminophen. Metab Brain Dis 24: 383-394.   DOI
20 Biaglow JE, Varnes ME, Roizen-Towle L, Clark EP, Epp ER, Astor MB, Hall EJ. 1986. Biochemistry of reduction of nitro heterocycles. Biochem Pharmacol 35: 77-90.   DOI
21 Vermeulen NPE, Bessems JGM, Van de Straat R. 1992. Molecular aspects of paracetamol-induced hepatotoxicty and its mechanism-based prevention. Drug Metab Rev 24: 367-407.   DOI
22 Sun J, Schnackenberg LK, Beger RD. 2009. Studies of acetaminophen and metabolites in urine and their correlations with toxicity using metabolomics. Drug Metab Lett 3: 130-136.   DOI
23 Marchetti A, Rossiter R. 2009. Managing acute acetaminophen poisoning with oral versus intravenous N-acetylcysteine: a provider-perspective cost analysis. J Med Econ 12: 384-391.   DOI
24 Schwabe RF, Uchinami H, Qian T, Bennett BL, Lemasters JJ, Brenner DA. 2004. Differential requirement for c-Jun NH2-terminal kinase in TNF$\alpha$- and Fas-mediated apoptosis in hepatocytes. FASEB J 18: 720-722.
25 Clissold SP. 1986. Pracetamol and phenacetin. Drugs 4: 46-59.
26 Hinson JA, Roberts DW, James LP. 2010. Mechanisms of acetaminophen-induced liver necrosis. Handb Exp Pharmacol 196: 369-405.   DOI
27 Jaeschke H, Bajt ML. 2006. Intracellular signaling mechanisms of acetaminophen-induced liver cell death. Toxicol Sci 89: 31-41.   DOI
28 Yokozawa T, Dong E, Chung HY, Oura H, Nakagawa H. 1997. Inhibitory effect of green tea on injury to a cultured renal epithelial cell line, LLC-PK1. Biosci Biotechnol Biochem 61: 204-206.   DOI
29 Lee KJ, You HJ, Park SJ, Chung YC, Jeong TC, Jeong HG. 2001. Hepatoprotective effects of Platycodon grandiflofum on acetaminophen-induced liver damage in mice. Cancer Lett 174: 73-81.   DOI
30 Lee YS, Han OK, Jeon TW, Lee ES, Kim KJ, Park CW, Kim HJ. 2002. Effect of Astrahali radix extract on acetaminophen-induced hepatotoxicity in mice. Korean J Oriental Physiol Pathol 16: 707-713.
31 Levine RL, Garland D, Oliver CN, Amici A, Climet I, Lenz AG, Ahn BW, Shaltiel S, Stadtman ER. 1990. Determination of carbony content in oxidatively modified proteins. Methods Enzymol 186: 464-478.   DOI
32 Sugiyama T, Sadzuka Y. 2004. Theanine, a specific glutamate derivative in green tea, reduces the adverse reactions of doxorubicin by changing the glutathione level. Cancer Lett 212: 177-184.   DOI
33 Yeung JH, Chiu LC, Ooi VE. 1994. Effect of polysaccharide peptide (PSP) on glutathion and protection against paracetamol-induced hepatotoxicity in the rat. Methods Find Exp Clin Pharmacol 16: 723-729.
34 Cohen SD, Khairallah EA. 1997. Selective protein arylation and acetaminophen-induced hepatotoxicty. Prug Metab Rev 29: 59-101.   DOI
35 Lee KJ, You HJ, Park SJ, Kim YS, Chung YC, Jeong TC, Jeong HG. 2001. Hepatoprotective effects of Platycodon grandiflorum on acetaminophen-induced liver damage in mice. Cancer Lett 174: 73-81.   DOI