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Protective Effect of Juglans regia L. Walnut Extract Against Oxidative DNA Damage

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Abstract

Walnuts (Juglans regia L.) are relevant components of the Mediterranean diet providing important macronutrients, micronutrients and other bioactive constituents including unsaturated fatty acids, proteins, fiber, vitamins, minerals, phytosterols and polyphenols. Although the walnut beneficial effects in human health are widely recognized by a lot of epidemiologic studies very little is known regarding its effect on damaged DNA. The aim of the present study was to investigate the effect of Juglans regia L. ethanolic extract from kernel on the induction of DNA strand breaks by thiol/Fe3+/O2 mixed function oxidase, tert-butyl hydroperoxide or UVC radiations in acellular and cellular models. Plasmid DNA cleavage and fast Halo assay were used to monitor oxidative damage to DNA. Both approaches showed protection of oxidatively injured DNA. These results agree with a lot of scientific proofs which recommend walnut as dietary adjunct in health promotion and prevention as well as in treatment of lifestyle-related oxidative diseases.

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Abbreviations

ANOVA:

analysis of variance

CPD:

cyclobutane pyrimidine dimer

DMEM:

Dulbecco’s modified eagle medium

DMSO:

dimethylsulphoxide

DSB:

double strand break

DTT:

1,4-dithiothreitol

EDTA:

ethylenediaminetetraacetic acid

EtBr:

ethidium bromide

HEPES:

(4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid)

JRE:

Junglans regia ethanolic extract

MFO:

thiol/Fe3+/O2 mixed-function oxidase

MTT:

(3-(4,5-dimethylthiazol-2-yl)-2,5-dipheniltetrazolium bromide)

NDF:

nuclear diffusion factor

ON:

overnight

PBS:

phosphate buffered saline

ROS:

reactive oxygen species

SSB:

single strand break

tBOOH:

tert-buthylhydroperoxide

UVC:

ultraviolet C

References

  1. Beer R, Kaiser F, Schmidt K, Ammann B, Carraro G, Grisa E, Tinner W (2008) Vegetation history of the walnut forests in Kyrgyzstan (Central Asia). Quat Sc Rev 27:621–632

    Article  Google Scholar 

  2. Ducci F, Rogatis A, Proietti R (1997) Protezione delle risorse genetiche di Juglans regia L. Ann Ist Sper Selv 25(26):35–55

    Google Scholar 

  3. Martınez ML, Labuckas DO, Lamarque AL, Maestri DM (2010) Walnut (Juglans regia L.): genetic resources, chemistry, by-products. J Sci Food Agric 90:1959–1967

    Google Scholar 

  4. Bolling BW, McKay DL, Blumberg JB (2010) The phytochemical composition and antioxidant actions of tree nuts. Asia Pac J Clin Nutr 19:117–123

    CAS  Google Scholar 

  5. Amaral JS, Casal S, Pereira JA, Seabra R, Oliveira BPP (2003) Determination of sterol and fatty acid compositions, oxidative stability, and nutritional value of six walnut (Juglans regia L.) cultivars grown in Portugal. J Agric Food Chem 51:7698–7702

    Article  CAS  Google Scholar 

  6. Jenab M, Sabate J, Slimani N et al (2006) Consumption and portion sizes of tree nuts, peanuts and seeds in the European prospective investigation into cancer and nutrition (EPIC) cohorts from 10 European countries. Br J Nutr 96:S12–S23

    Article  CAS  Google Scholar 

  7. Sabate J, Fraser GE, Burke K, Knutsen SFM, Bennett H, Lindsted KD (1993) Effects of walnuts on serum lipid levels and blood pressure in normal men. N Engl J Med 328:603–607. doi:10.1056/NEJM199303043280902

    Article  CAS  Google Scholar 

  8. Zambon D, Sabate J, Munoz S, Campero B, Casals E, Merlos M, Laguna J, Ros E (2000) Substituting walnuts for monounsaturated fat improves the serum lipid profile of hypercholesterolemic men and women: a randomised crossover. Trial Ann Intern Med 137:538–546

    Article  Google Scholar 

  9. Kris-Etherton PM, Zhao G, Binkoski AE, Coval SM, Etherton TD (2001) The effects of nuts on coronary heart disease risk. Nutr Rev 59:103–111

    Article  CAS  Google Scholar 

  10. Cortes B, Nunez I, Cofan M, Gilabert R, Perez-Heras A, Casals E, Deulofeu R, Ros E (2006) Acute effects of high-fat meals enriched with walnuts or olive oil on postprandial endothelial function. J Am Coll Cardiol 48:1666–1671. doi:10.1016/j.jacc.2006.06.057

    Article  CAS  Google Scholar 

  11. Kris-Etherton PM, Hu FB, Ros E, Sabaté J (2008) The role of tree nuts and peanuts in the prevention of coronary heart disease: multiple potential mechanisms. J Nutr 138:1746S–1751S

    CAS  Google Scholar 

  12. Jenkins DJA, Hu FB, Tapsell LC, Josse AR, Kendall CWC (2008) Possible benefit of nuts in type 2 diabetes. J Nutr 138:1752S–1756S

    CAS  Google Scholar 

  13. Casas-Agustench P, López-Uriarte P, Bullo M, Ros E, Cabré-Vila JJ, Salas-Salvadó J (2011) Effects of one serving of mixed nuts on serum lipids, insulin resistance and inflammatory markers in patients with the metabolic syndrome. Nutr Metab Cardiovasc Dis 21:126–135. doi:10.1016/j.numecd.2009.08.005

    Article  CAS  Google Scholar 

  14. Jenab M, Ferrari P, Slimani N, Norat T, Casagrande C, Overad K (2004) Association of nut and seed intake with colorectal cancer risk in the European prospective investigation into cancer and nutrition. Cancer Epidemiol Biomark Prev 13:1595–1603

    CAS  Google Scholar 

  15. Hardman WE (2014) Walnuts have potential for cancer prevention and treatment in mice. J Nutr 144:555S–560S. doi:10.3945/jn.113.188466

    Article  CAS  Google Scholar 

  16. Nakanishi M, Chen Y, Qendro V, Miyamoto S, Weinstock E, Weinstock GM, Rosenberg DW (2016) Effects of walnut consumption on colon carcinogenesis and microbial community structure. Cancer Prev Res (Phila) 9:692–703. doi:10.1158/1940-6207.CAPR-16-0026

  17. Tsoukas MA, Ko BJ, Witte TR, Dincer F, Hardman WE, Mantzoros CS (2015) Dietary walnut suppression of colorectal cancer in mice: mediation by miRNA patterns and fatty acid incorporation. J Nutr Biochem 26:776–783. doi:10.1016/j.jnutbio.2015.02.009.1

    Article  CAS  Google Scholar 

  18. Vadivel V, Kunyanga CN, Biesalski HK (2012) Health benefits of nut consumption with special reference to body weight control. Nutrition 28:1089–1097. doi:10.1016/j.nut.2012.01.004

    Article  CAS  Google Scholar 

  19. Haider S, Batool Z, Tabassum S, Perveen T, Saleem S, Naqvi F, Javed H, Haleem DJ (2011) Effects of walnuts (Juglans regia) on learning and memory functions. Plant Foods Hum Nutr 66:335–340. doi:10.1007/s1130-011-0260-2

    Article  CAS  Google Scholar 

  20. Laubertová L, Koňariková K, Gbelcová H, Duracková Z, Zitnanová I (2014) Effect of walnut oil on hyperglycemia-induced oxidative stress and pro-inflammatory cytokines production. Eur J Nutr 54:291-299. doi:10.1007/s00394-014-0710-3

  21. Prieto P, Pineda M, Aguilar M (1999) Spectrophotometric quantitation of antioxidant capacity through the formation of a phosphomolybdenum complex: specific application to the determination of vitamin E. Anal Biochem 269:337–341. doi:10.1006/abio.1999.4019

    Article  CAS  Google Scholar 

  22. Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Meth 65(1–2):55–63

    Article  CAS  Google Scholar 

  23. Sestili P, Martinelli C, Stocchi V (2006) The fast Halo assay: an improved method to quantify genomic DNA strand breakage at the single-cell level. Mutat Res 607:205–214. doi:10.1016/j.mrgentox.2006.04.018

    Article  CAS  Google Scholar 

  24. Svobodovà A, Walterovà D, Psotovà J (2006) Influence of Silymarin and its flavolignans on H2O2-induced oxidative stress in human keratinocytes and mouse. Burns 32(8):973-979. doi:10.1016/j.burns.2006.04.004

  25. Valko M, Leibfritz D, Moncola J, Cronin MD (2007) Free radicals and antioxidants in normal physiological functions and human disease. Review. Int J Biochem Cell Biol 39:44–84. doi:10.1016/j.biocel.2006.07.001

    Article  CAS  Google Scholar 

  26. Albishi T, John JA, Al-Khalifa AS, Shahidi F (2013) Antioxidant, anti-inflammatory and DNA scission inhibitory activities of phenolic compounds in selected onion and potato varieties. J Funct Foods 5:930–939. doi:10.1016/j.jff.2013.02.005

    Article  CAS  Google Scholar 

  27. Chandrasekara A, Shahidi F (2011) Antiproliferative potential and DNA scission inhibitory activity of phenolics from whole millet grains. J Funct Foods 3:159–170. doi:10.1016/j.jff.2011.03.008

    Article  CAS  Google Scholar 

  28. Lin S, Yang B, Chen F, Jiang G, Li Q, Duan X et al (2012) Enhanced DPPH radical scavenging activity and DNA protection effect of litchi pericarp extract by Aspergillus awamori bioconversion. Chem Cent J 6:108. doi:10.1186/1752-153X-6-108

  29. Breen AP, Murphy JA (1995) Reactions of oxyl radicals with DNA. Free Radic Biol Med 18:1033–1077

    Article  CAS  Google Scholar 

  30. Ward JF (1985) Biochemistry of DNA lesions. Radiat Res 104:S103–S111

    Article  CAS  Google Scholar 

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Acknowledgements

The present research was supported by funds of the University of Urbino Carlo Bo.

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Correspondence to Lucia Potenza.

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This article does not contain any studies with human subjects or animal models.

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Calcabrini, C., De Bellis, R., Mancini, U. et al. Protective Effect of Juglans regia L. Walnut Extract Against Oxidative DNA Damage. Plant Foods Hum Nutr 72, 192–197 (2017). https://doi.org/10.1007/s11130-017-0609-2

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