Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
JCR Impact Factor (IF) – 2.1
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Index Copernicus  – 161.11; MNiSW – 70 pts

ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
Periodicity – monthly

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Advances in Clinical and Experimental Medicine

2017, vol. 26, nr 3, May-June, p. 393–399

doi: 10.17219/acem/61834

Publication type: original article

Language: English

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Relationship between dietary antioxidant index (DAI) and antioxidants level in plasma of Kraków inhabitants

Emilia Kolarzyk1,2,A,C,F, Agata Pietrzycka3,B,E,F, Joanna Zając1,C,D,F, Joanna Morawiecka-Baranek4,C,F

1 Department of Hygiene and Dietetics, Jagiellonian University Medical College, Kraków, Poland

2 Cracow Higher School of Health Promotion, Kraków, Poland

3 Department of Pharmacobiology, Jagiellonian University Medical College, Kraków, Poland

4 The Regional Specialist Children’s Hospital of St. Ludwig, Kraków, Poland

Abstract

Background. Some literature data indicate that antioxidant-rich food may significantly increase antioxidants in serum and decrease the oxidative stress but results are ambiguous.
Objectives. The aim of this study was to estimate the total antioxidant capacity of food intake among the inhabitants of Kraków, Poland on the basis of dietary antioxidant index (DAI) and evaluation the relation between DAI and the level of antioxidants in plasma.
Material and Methods. Examination included 70 (37 women and 33 men) non-smoking inhabitants of Krakow aged 46.4 ± 13.7 years. DAI was investigated on the basis of Food Frequency Questionnaire including 145 food items. DAI was measured using the method by Benzi and expressed as FRAP (mMol/L). In plasma samples total antioxidant status (TAS) expressed as FRAP and malondialdehyde (MDA) concentration as a marker of lipids peroxidation were measured.
Results. The mean value of DAI of all examined persons was 46.74 ± 25.5 mMol/L (in female group: 54.13 ± 27.7 mMol/L; in male group: 37.83 ± 19.5 mMol/L; p < 0.05). The highest contribution in total DWA value had fruits (48.7%) opposite to vegetables (9.3%). Statistically significant positive correlations between DAI and FRAP in plasma was found in all: r = 0.42 and in female: r = 0.54 groups (not significant in men group: r = 0.20). Statistically significant negative correlation of DAI with MDA (malonylaldehyde) in female (-0.49) and male (-0.51) groups.
Conclusion. The obtained results confirmed the hypothesis that the intake of antioxidants in daily diet (measured as DAI) might increase antioxidants defense (measured by TAC as FRAP) and decrease oxidative stress (measured by MDA concentration in plasma). The dietary modification towards higher consumption of antioxidants (especially in men) should be highlighted in prevention of diseases in which oxidative stress play considerable role.

Key words

FRAP, MDA, healthy people, dietary antioxidant index, Food Frequency Questionnaire

References (30)

  1. Lobo V, Patil A, Phatak A, Chandra N. Free radicals, antioxidants and functional foods: Impact on human health. Pharmacogn Rev. 2010;4:118–126.
  2. Kalam S, Gul MZ, Singh R, Ankati S. Free radicals: Implications in etiology of chronic diseases and their amelioration through nutraceuticals. Pharmacologia. 2015;6:11–20.
  3. El-Beltagi HS, Mohamed HI. Reactive oxygen species, lipid peroxidation and antioxidative defense mechanism. Not Bot Horti Agrobo. 2013;41:44–57.
  4. Zelko I, Mariani T, Folz R. Superoxide dismutase multigene family: A comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression. Free Radic Biol Med. 2002;33:337–349.
  5. Johnson F, Giulivi C. Superoxide dismutases and their impact upon human health. Mol Aspects Med. 2005;26:340–352.
  6. Chelikani P, Fita I, Loewen PC. Diversity of structures and properties among catalases. Cell Mol Life Sci. 2004;61:192–208.
  7. Hayes J, Flanagan J, Jowsey I. Glutathione transferases. Ann Rev Pharmacol Toxicol. 2005;45:51–88.
  8. Padayatty S, Katz A, Wang Y, Eck P, Kwon O, Lee J. Vitamin C as an antioxidant: Evaluation of its role in disease prevention. J Am Coll Nutr. 2003;22:18–35.
  9. Clarke MW, Burnett JR, Croft KD. Vitamin E in human health and disease. Crit Rev Clin Lab Sci. 2008;45:417–450.
  10. Tinggi U. Selenium. Its role as antioxidant in human health. Environ Health Prev Med. 2008;13:102–108.
  11. Zilica SC, Zita VH, Sukalovic S, et al. Anti‐oxidant activity of small grain cereals caused by phenolics and lipid soluble antioxi‐dants. J Cereal Sci. 2011;54:417–424.
  12. Linares E, Thimonier C, Degre M. The effect of neopuntia(r) on blood lipid parameters-risk factors for the metabolic syndrome (syndrome x). Adv Ther. 2007;24:1115–1125.
  13. Ozkanlar S, Akcay F. Antioxidant vitamins in atherosclerosis–animal experiments and clinical studies. Adv Clin Exp Med. 2012;21:115–123.
  14. Landete JM. Dietary intake of natural antioxidants: Vitamins and polyphenols. Crit Rev Food Sci Nutr. 2013;53:706–721.
  15. Satia JA, Watters JL, Galanko JA. Validation of an antioxidant nutrient questionnaire in Whites and African Americans. J Am Diet Assoc. 2009;109;502–508.
  16. Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: The FRAP assay. Anal Biochem. 1996;239:70–76.
  17. Esterbauer H, Cheeseman KH. Determination of aldehydic lipid peroxidation products: Malonaldehyde and 4-hydroxynonenal. Methods Enzymol. 1990;186:407–421.
  18. Wasowicz W, Neve J, Peretz A. Optimized steps in fluorometric determination of thiobarbituric acid-reactive substances in serum: Importance of extraction pH and influence of sample preservation and storage. Clin Chem. 1993;39:2522–2526.
  19. http://www.izz.waw.pl
  20. Wawrzyniak A, Krotki M, Stoparczyk B. Właściwości antyoksydacyjne owoców i warzyw. Med Rodz. 2011;1:19–23.
  21. Człapka-Matysik, Kostrzewa-Tarnowska A, Bajerska J. Potencjał antyoksydacyjny racji pokarmowych pacjentów ze zdiagnozowanymi chorobami układu krążenia. Zyw Nauka Technol Jakosc. 2009;4:312–319.
  22. Butnariu M, Caunii A. Design management of functional foods for quality of life improvement. AAEM. 2013;20:736–741.
  23. Chun OK, Floegel A, Chung SJ, Chung CE, Song WO, Koo S. Estimation of antioxidant intakes from diet and supplements in U.S adults. J Nutr. 2010;140:317–324.
  24. Cook NR, Albert CM, Gaziano JM, et al. A randomized factorial trial of vitamins C and E and beta carotene in the secondary prevention of cardiovascular events in women: Results from the women’s antioxidant cardiovascular study. Arch Intern Med. 2007;167:1610–1618.
  25. Lee IM, Cook NR, Gaziano JM, et al. Vitamin E in the primary prevention of cardiovascular disease and cancer: The women’s health study: A randomized controlled trial. JAMA. 2005;294:56–65.
  26. Klein EA, Thompson IM Jr, Tangen CM, et al. Vitamin E and the risk of prostate cancer: The selenium and vitamin E cancer prevention trial (SELECT). JAMA. 2011;306:1549–1556.
  27. Jerome-Morais A, Diamond AM, Wright ME. Dietary supplements and human health: For better or for worse? Mol Nutr Food Res. 2011;55:122–135.
  28. Joshipura KJ, Hu FB, Manson JE, et al. The effect of fruit and vegetable intake on risk for coronary heart disease. J Nutr. 2006;136:2588–2593.
  29. Wang X, Ouyang Y, Liu J, et al. Fruit and vegetable consumption and mortality from all causes, cardiovascular disease, and cancer: Systematic review and dose-response meta-analysis of prospective Cohort studies. BMJ. 2014;349:g4490.
  30. Ayala A, Muñoz MF, Argüelles S. Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev. 2014:360438. doi: 10.1155/2014/360438. Epub 2014 May 8.