Instant coffee with high chlorogenic acid levels protects humans against oxidative damage of macromolecules

被引:112
作者
Hoelzl, Christine [1 ]
Knasmueller, Siegfried [1 ]
Wagner, Karl-Heinz [2 ]
Elbling, Leonilla [1 ]
Huber, Wolfgang [1 ]
Kager, Nina [1 ]
Ferk, Franziska [1 ]
Ehrlich, Veronika [1 ]
Nersesyan, Armen [1 ]
Neubauer, Oliver [2 ]
Desmarchelier, Aurelien [3 ]
Marin-Kuan, Maricel [3 ]
Delatour, Thierry [3 ]
Verguet, Clotilde [3 ]
Bezencon, Claudine [3 ]
Besson, Amelie [3 ]
Grathwohl, Dominik [3 ]
Simic, Tatjana [4 ]
Kundi, Michael [5 ]
Schilter, Benoit [3 ]
Cavin, Christophe [3 ]
机构
[1] Med Univ Vienna, Inst Canc Res, Dept Med 1, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Nutrit Sci, Vienna, Austria
[3] Nestle Res Ctr, CH-1000 Lausanne, Switzerland
[4] Univ Belgrade, Fac Med, Inst Med & Clin Biochem, Belgrade, Serbia
[5] Med Univ Vienna, Inst Environm Hlth, Vienna, Austria
关键词
Antioxidants; Chlorogenic acids; Instant coffee; Intervention trial; INDUCED DNA-DAMAGE; GLUTATHIONE S-TRANSFERASES; COMET ASSAY; IN-VITRO; ANTIOXIDANT CAPACITY; LIPID-PEROXIDATION; PLASMA; CONSUMPTION; DISEASE; HEALTH;
D O I
10.1002/mnfr.201000048
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Scope: Coffee is among the most frequently consumed beverages. Its consumption is inversely associated to the incidence of diseases related to reactive oxygen species; the phenomenon may be due to its antioxidant properties. Our primary objective was to investigate the impact of consumption of a coffee containing high levels of chlorogenic acids on the oxidation of proteins, DNA and membrane lipids; additionally, other redox biomarkers were monitored in an intervention trial. Methods and results: The treatment group (n = 36) consumed instant coffee co-extracted from green and roasted beans, whereas the control consumed water (800 mL/P/day, 5 days). A global statistical analysis of four main biomarkers selected as primary outcomes showed that the overall changes are significant. 8-Isoprostaglandin F2 alpha in urine declined by 15.3%, 3-nitrotyrosine was decreased by 16.1%, DNA migration due to oxidized purines and pyrimidines was (not significantly) reduced in lymphocytes by 12.5 and 14.1%. Other markers such as the total antioxidant capacity were moderately increased; e.g. LDL and malondialdehyde were shifted towards a non-significant reduction. Conclusion: The oxidation of DNA, lipids and proteins associated with the incidence of various diseases and the protection against their oxidative damage may be indicative for beneficial health effects of coffee.
引用
收藏
页码:1722 / 1733
页数:12
相关论文
共 64 条
[1]
OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[2]
[Anonymous], 1994, ZELL GEWEBEKULTUR
[3]
BAKURADZE T, 2009, 4 INT C POL HLTH U L, P266
[4]
Roasting effects on formation mechanisms of coffee brew melanoidins [J].
Bekedam, E. Koen ;
Loots, Mirjam J. ;
Schols, Henk A. ;
Van Boekel, Martinus A. J. S. ;
Smit, Gerrit .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (16) :7138-7145
[5]
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[6]
Coffee consumption protects human lymphocytes against oxidative and 3-amino-1-methyl-5H-pyrido [4,3-b]indole acetate (Trp-P-2) induced DNA-damage:: Results of an experimental study with human volunteers [J].
Bichler, J. ;
Cavin, C. ;
Simic, T. ;
Chakraborty, A. ;
Ferk, F. ;
Hoelzl, C. ;
Schulte-Hermann, R. ;
Kundi, M. ;
Haidinger, G. ;
Angelis, K. ;
Knasmueller, S. .
FOOD AND CHEMICAL TOXICOLOGY, 2007, 45 (08) :1428-1436
[7]
Coffee and cardiovascular disease:: In vitro, cellular, animal, and human studies [J].
Bonita, Jennifer Stella ;
Mandarano, Michael ;
Shuta, Donna ;
Vinson, Joe .
PHARMACOLOGICAL RESEARCH, 2007, 55 (03) :187-198
[8]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]
Induction of Nrf2-mediated cellular defenses and alteration of phase I activities as mechanisms of chemoprotective effects of coffee in the liver [J].
Cavin, C. ;
Marin-Kuan, M. ;
Langouet, S. ;
Bezencon, C. ;
Guignard, G. ;
Verguet, C. ;
Piguet, D. ;
Holzhaeuser, D. ;
Cornaz, R. ;
Schilter, B. .
FOOD AND CHEMICAL TOXICOLOGY, 2008, 46 (04) :1239-1248
[10]
Collins A, 1997, ENVIRON MOL MUTAGEN, V30, P139, DOI 10.1002/(SICI)1098-2280(1997)30:2<139::AID-EM6>3.0.CO