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Effect of Diet Supplemented with Quinoa Seeds on Oxidative Status in Plasma and Selected Tissues of High Fructose-Fed Rats

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Abstract

Oxidative stress plays an important role as a mediator of damage produced by fructose metabolism. This work was designed to investigate the effect of diet supplemented with quinoa seeds on oxidative stress in plasma, heart, kidney, liver, spleen, lung, testis and pancreas of fructose administered rats. Fructose administration (310 g/kg fodder for 5 weeks) caused oxidative stress that was manifested by the increase in plasma malondialdehyde (MDA) (p<0.05), and by the non-significant changes in the enzymatic antioxidant potential in plasma and most of tissues. Co-administration of quinoa seeds (310 g/kg fodder) maintained normal activities of some enzymes. It also influenced the oxidative stress as was evidenced by decreasing MDA in plasma, and decreasing the activities of antioxidant enzymes (erythrocyte superoxide dismutase - eSOD, catalase -CAT, plasma glutathione peroxidase - pGPX). These findings demonstrate that quinoa seeds can act as a moderate protective agent against potential of fructose-induced changes in rats by reducing lipid peroxidation and by enhancing the antioxidant capacity of blood (plasma) and heart, kidney, testis, lung and pancreas.

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Abbreviations

CAT:

catalase

eSOD:

erythrocyte superoxide dismutase

GPX:

glutathione peroxidase

FRAP:

ferric reducing ability of plasma

MDA:

malondialdehyde

pGPX:

plasma glutathione peroxidase

SOD:

superoxide dismutase

References

  1. Basciano H, Federico L, Adeli K (2005) Fructose, insulin resistance, and metabolic dyslipidemia. Nutr Metab 2:1–14

    Article  Google Scholar 

  2. Isganaitis E, Lustig RH (2005) Fast food, central nervous system insulin resistance and obesity. Arterioscler Thromb Vasc Biol 25:2451–2462

    Article  CAS  Google Scholar 

  3. Girard A, Madani S, El Boustani ES, Belleville J, Prost J (2005) Changes in lipid metabolism and antioxidant defense status in spontaneously hypertensive rats and Wistar rats fed a diet enriched with fructose and saturated fatty acids. Nutrition 21:240–248

    Article  CAS  Google Scholar 

  4. Gorinstein S, Vargas OJM, Jaramillo NO, Salas IA, Ayala AM, Arancibia-Avila P, Toledo F, Katrich E, Trakhtenberg S (2007) The total polyphenols and the antioxidant potentials of some selected cereals and pseudocereals. Eur Food Res Technol 225:321–328

    Article  CAS  Google Scholar 

  5. Paśko P, Bartoń H, Zagrodzki P, Gorinstein S, Fołta M, Zachwieja Z (2009) Anthocyanins, total polyphenols and antioxidant activity in amaranth and quinoa seeds and sprouts during their growth. Food Chem 115:994–998

    Article  Google Scholar 

  6. Ryan E, Galvin K, O’Connor T, Maguire A, O’Brien N (2007) Phytosterol, squalene, tocopherol content and fatty acid profile of selected seeds, grains, and legumes. Plant Foods Hum Nutr 62:85–91

    Article  CAS  Google Scholar 

  7. Zagrodzki P, Joniec A, Gawlik M, Gawlik M, Krośniak M, Fołta M, Bartoń H, Paśko P, Chłopicka J, Zachwieja Z (2007) High fructose model of oxidative stress and metabolic disturbances in rats. Part I. Antioxidant status of rats’ tissues. Bull Vet Inst Pulawy 51:407–412

    Google Scholar 

  8. Busserolles J, Gueux E, Rock E, Mazur A, Rayssiguier Y (2002) Substituting honey for refined carbohydrates protects rats from hypertriglyceridemic and prooxidative effects of fructose. J Nutr 132:3379–3382

    CAS  Google Scholar 

  9. Farombi EO, Hansen M, Ravn-Haren G, Møller P, Dragsted LO (2004) Commonly consumed and naturally occurring dietary substances affect biomarkers of oxidative stress and DNA damage in healthy rats. Food Chem Toxicol 42:1315–1322

    Article  CAS  Google Scholar 

  10. Qin F, Liu YX, Zhao HW, Huang X, Ren P, Zhu ZY (2009) Chinese medicinal formula Guan-Xin-Er-Hao protects the heart against oxidative stress induced by acute ischemic myocardial injury in rats. Phytomedicine 16:215–221

    Article  CAS  Google Scholar 

  11. Błaszczyk I, Grucka-Mamczar E, Kasperczyk S, Brikner E (2008) Influence of fluoride on rat kidney antioxidant system: effect of methionine and vitamin E. Biol Trace Elem Res 121:51–59

    Article  Google Scholar 

  12. Bouderbala S, Lamri-Senhadji M, Prost J, Lacaille-Dubois M, Bouchenak M (2008) Changes in antioxidant defense status in hypercholesterolemic rats treated with Ajuga iva. Phytomedicine 15:453–61

    Article  CAS  Google Scholar 

  13. Gonzalez J, Roldan A, Gallardo M, Escudero T, Prado F (1989) Quantitative determination of chemical compounds with nutritional value from Inca crops: Chenopodium chinoa (quinoa). Plant Foods Hum Nutr 39:331–337

    Article  CAS  Google Scholar 

  14. Saravanan R, Pugalendi V (2006) Impact of ursolic acid on chronic ethanol-induced oxidative stress in the rat heart. Pharmacol Rep 58:41–47

    CAS  Google Scholar 

  15. Kumar HS, Anandan R (2007) Biochemical studies on the cardioprotective effect of glutamine on tissue antioxidant defense system in isoprenaline-induced myocardial infarction in rats. J Clin Biochem Nutr 40:49–55

    Article  CAS  Google Scholar 

  16. Mehmetcik G, Özdemirler G, Kocak-Toker N, Cevikbas U, Uysal M (2008) Effect of pretreatment with artichoke extract on carbon tetrachloride—induced liver injury and oxidative stress. Exp Toxicol Pathol 60:475–480

    Article  Google Scholar 

  17. Kaleem M, Asif M, Ahmed QU, Bano B (2006) Antidiabetic and antioxidant activity of Annona squamosa extract in streptozotocin-induced diabetic rats. Singapore Med J 47:670–675

    CAS  Google Scholar 

  18. Talas Z, Ozdemir I, Yilmaz I, Gok Y (2009) Antioxidative effects of novel synthetic organoselenium compound in rat lung and kidney. Ecotoxicol Environ Saf 72:916–921

    Article  CAS  Google Scholar 

  19. Wongmekiat O, Leelarugrayub N, Thamprasert K (2008) Beneficial effect of shallot extract on cyclosporine nephrotoxicity in rats. Food Chem Toxicol 46:1844–1850

    Article  CAS  Google Scholar 

  20. Medan MS, Absy G, Zeidan AE, Khalil MH, Khalifa HH, Abdel-Salaam AM, Abdel-Khalek TM (2008) Survival and fertility rate of cooled dromedary camel spermatozoa supplemented with catalase enzyme. J Reprod Dev 54:84–89

    Article  CAS  Google Scholar 

  21. Melis MS (1999) Effects of chronic administration of Stevia rebaudiana on fertility in rats. J Ethnopharmacol 167:157–161

    Article  Google Scholar 

  22. Türk G, Sönmez M, Aydin M, Yüce A, Gür S, Yüksel M, Aksu E, Aksoy H (2008) Effects of pomegranate juice consumption on sperm quality, spermatogenic cell density, antioxidant activity and testosterone level in male rats. Clin Nutr 27:289–296

    Article  Google Scholar 

  23. Hemmati A, Nazari Z, Samei M (2008) A comparative study of grape seed extract and vitamin E effects on silica—induced pulmonary fibrosis in rats. Pulm Pharmacol Ther 21:668–674

    Article  CAS  Google Scholar 

  24. Coskun O, Ocakci A, Bayraktaroglu T, Kanter M (2004) Exercise training prevents and protects streptozotocin–induced oxidative stress and B–cell damage in rat pancreas. Tohoku J Exp Med 203:145–154

    Article  CAS  Google Scholar 

  25. Czakó L, Hegyi P, Takács T, Góg C, Farkas A, Mandy Y, Varga IS, Tiszlavicz L, Lonovics J (2004) Effects of octreotide on acute necrotizing pancreatitis in rabbits. World J Gastroenterol 10:2082–2086

    Google Scholar 

  26. Parthasarathy NJ, Kumar RS, Manikandan S, Devi RS (2006) Methanol-induced oxidative stress in rat lymphoid organs. J Occup Health 48:20–27

    Article  CAS  Google Scholar 

  27. Jung CH, Seog HM, Choi IW, Choi HD, Cho HY (2005) Effects of wild ginseng (Panax ginseng C.A. Meyer) leaves on lipid peroxidation levels and antioxidant enzyme activities in streptozotocin diabetic rats. J Ethnopharmacol 98:245–250

    Article  Google Scholar 

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Acknowledgement

This work was supported in part by the grant PBZ-KBN 094/P06/2003/08 from Polish Ministry of Science and Higher Education.

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Correspondence to Pawel Pasko.

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Pasko, P., Barton, H., Zagrodzki, P. et al. Effect of Diet Supplemented with Quinoa Seeds on Oxidative Status in Plasma and Selected Tissues of High Fructose-Fed Rats. Plant Foods Hum Nutr 65, 146–151 (2010). https://doi.org/10.1007/s11130-010-0164-6

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  • DOI: https://doi.org/10.1007/s11130-010-0164-6

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