Skip to main content
Log in

Amaranth Peptides from Simulated Gastrointestinal Digestion: Antioxidant Activity Against Reactive Species

  • Original Paper
  • Published:
Plant Foods for Human Nutrition Aims and scope Submit manuscript

Abstract

We evaluated the capacity of simulated gastrointestinal digests or alcalase hydrolysates of protein isolates from amaranth to scavenge diverse physiologically relevant reactive species. The more active hydrolysate was obtained with the former method. Moreover, a prior alcalase treatment of the isolate followed by the same simulated gastrointestinal digestion did not improve the antioxidant capacity in any of the assays performed and even produced a negative effect under some conditions. Gastrointestinal digestion produced a strong increment in the scavenging capacity against peroxyl radicals (ORAC assay), hydroxyl radicals (ESR-OH assay), and peroxynitrites; thus decreasing the IC50 values to approximately 20, 25, and 20 %, respectively, of the levels attained with the nonhydrolyzed proteins. Metal chelation (HORAC assay) also enhanced respect to isolate levels, but to a lesser extent (decreasing IC50 values to only 50 %). The nitric-oxide– and superoxide-scavenging capacities of the digests were not relevant with respect to the methodologies used. The gastrointestinal digests from amaranth proteins acted against reactive species by different mechanisms, thus indicating the protein isolate to be a potential polyfunctional antioxidant ingredient.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Halliwell B, Gutteridge J (1999) Free rad in biology and med. Clarendon, Oxford

    Google Scholar 

  2. Kohen R, Nyska A (2002) Oxidation of biological systems: oxidative stress phenomena, antioxidants, redox reactions, and methods for their quantification. Toxicol Pathol 30:620–650

    Article  CAS  Google Scholar 

  3. Noguchi N, Watanabe A, Shi H (2000) Diverse functions of antioxidants. Free Radic Res 33:809–817

    Article  CAS  Google Scholar 

  4. Hartmann R, Meisel H (2007) Food-derived peptides with biological activity: from research to food applications. Curr Opin Biotechnol 18:163–169

    Article  CAS  Google Scholar 

  5. Sarmadi B, Ismail A (2010) Antioxidative peptides from food proteins: a review. Peptides 31:1949–1956

    Article  CAS  Google Scholar 

  6. Udenigwe C, Aluko R (2012) Food protein-derived bioactive peptides: production, processing, and potential health benefits. J Food Sci 77(1):R11–R24

    Article  CAS  Google Scholar 

  7. Huerta Ocampo J, Barba de la Rosa A (2011) Amaranth: a pseudo-cereal with nutraceutical properties. Curr Nutr Food Sci 7:1–9

    Article  CAS  Google Scholar 

  8. Tironi V, Añón M (2010) Amaranth as a source of antioxidant peptides. Effect of proteolysis. Food Res Int 43:315–322

    Article  CAS  Google Scholar 

  9. Orsini Delgado M, Tironi V, Añón M (2011) Antioxidant activity of amaranth proteins or their hydrolysates under simulated gastrointestinal digestion. LWT Food Sci Technol 44:1752–1760

    Article  CAS  Google Scholar 

  10. Martinez N, Añón M (1996) Composition and structural characterization of amaranth protein isolates. An electrophoretic and calorimetric study. J Agric Food Chem 44:2523–2530

    Article  CAS  Google Scholar 

  11. Lowry O, Rosebrough N, Farr A, Randall R (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    CAS  Google Scholar 

  12. Ou B, Hampsch-Woodill M, Flanagan J et al (2002) Novel fluorometric assay for hydroxyl radical prevention capacity using fluorescein as the probe. J Agric Food Chem 50:2772–2777

    Article  CAS  Google Scholar 

  13. Moore J, Yin Y, Yu L (2006) Novel fluorometric assay for hydroxyl radical scavenging capacity (HOSC) estimation. J Agric Food Chem 54:617–626

    Article  CAS  Google Scholar 

  14. Hazra B, Biswas S, Mandal N (2008) Antioxidant and free radical scavenging activity of Spondias pinnata. BMC Complement Altern Med 8:63–73

    Article  Google Scholar 

  15. Oliveira M, Minotto J, Oliveira M et al (2010) Scavenging and antioxidant potential of physiological taurine concentrations against different reactive oxygen/nitrogen species. Pharmacol Rep 62:185–193

    Article  CAS  Google Scholar 

  16. Hughes M, Nicklin H (1968) The chemistry of peroxynitrites. Part I: kinetics of decompositions of peroxynitrous acid. J Chem Soc A:450–452

  17. Possel H, Noack H, Augustin W, Keilhof G, Wolf G (1997) 2,7-Dihydrodichlorofluorescein diacetate as a fluorescent marker for peroxynitrite formation. FEBS Lett 416:175–178

    Article  CAS  Google Scholar 

  18. Kooy N, Royall J, Ischlropoulos H (1997) Oxidation of 2′,7′-dichlorofluorescin by peroxynitrite. Free Radic Res 27:245–254

    Article  CAS  Google Scholar 

  19. Nakajima A, Matsuda E, Matsuda Y, Sameshima H, Ikenoue T (2012) Characteristics of the spin-trapping reaction of a free radical derived from AAPH: further development of the ORAC-ESR assay. Anal Bioanal Chem 403:1961–1970

    Article  CAS  Google Scholar 

  20. Ou B, Hampsch-Woodill M, Prior R (2001) Development and validation of an improved oxygen radical absorbance capacity assay using fluorescein as the fluorescent probe. J Agric Food Chem 49:4619–4626

    Article  CAS  Google Scholar 

  21. Kim G, Jang H, Kim C (2007) Antioxidant capacity of caseinophosphopeptides prepared from sodium caseinate using alcalase. Food Chem 104:1359–1365

    Article  CAS  Google Scholar 

  22. Samaranayaka A, Li-Chan E (2008) Autolysis assisted production of fish protein hydrolysates with antioxidant properties from pacific hake (Merluccius productus). Food Chem 107:768–776

    Article  CAS  Google Scholar 

  23. Zhou K, Caning C, Sun S (2013) Effects of rice protein hydrolysates prepared by microbial proteases and ultrafiltration on free radicals and meat lipid oxidation. LWT Food Sci Technol 50:331–335

    Article  CAS  Google Scholar 

  24. Silva F, O’Callagahan Y, O’Brien N, Netto F (2013) Antioxidant capacity of flaxseed products: the effect of in vitro digestion. Plant Foods Hum Nutr 68:24–30

    Article  CAS  Google Scholar 

  25. Minetti M, Pietraforte D, Di Stazi A, Mallozi C (1996) Nitric oxide-dependent NAD linkage to glyceraldehyde-3-phosphate dehydrogenase:possible involvement of a cysteine thiyl radical intermediate. Biochem J 319:369–375

    CAS  Google Scholar 

  26. Ma Y, Xiong Y, Zhai J, Zhu H, Dziubla T (2010) Fractionation and evaluation of radical scavenging peptides from in vitro digests of buckwheat protein. Food Chem 118:582–588

  27. Linxiang L, Abe Y, Kanagawa K et al (2007) Iron-chelating agents never suppress Fenton reaction but participate in quenching spin-trapped radicals. Anal Chim Acta 599:315–319

    Article  Google Scholar 

  28. Mendis E, Rajapakse N, Byun H, Kim S (2005) Investigation of jumbo squid (Dosidicus gigas) skin gelatin peptides for their in vitro antioxidant effects. Life Sci 70:2166–2178

  29. Zhong S, Ma C, Lin Y, Luo Y (2011) Antioxidant properties of peptide fractions from silver carp (Hypophthalmichthys molitrix) processing by-product protein hydrolysates evaluated by electron spin resonance spectrometry. Food Chem 126:1636–1642

    Article  CAS  Google Scholar 

  30. Ewing J, Janero D (1995) Microplate superoxide dismutase assay employing a nonenzymatic superoxide generator. Anal Biochem 232:243–248

    Article  CAS  Google Scholar 

  31. Moure A, Domínguez H, Parajo J (2006) Antioxidant properties of ultrafiltration-recovered soy protein fractions from industrial effluents and their hydrolysates. Process Biochem 41:447–456

    Article  CAS  Google Scholar 

  32. Quansah J, Udenigwe C, Saalia F, Yada R (2013) The effect of thermal and ultrasonic treatment on amino acid composition, radical scavenging and reducing potential of hydrolysates obtained from simulated gastrointestinal digestion of cowpea proteins. Plant Foods Hum Nutr 68:31–38

    Article  CAS  Google Scholar 

  33. Zhuang Y, Sun L (2011) Preparation of reactive oxygen scavenging peptides from tilapia (Oreochromis niloticus) skin gelatin: optimization using response surface methodology. J Food Sci 76(3):C483–C489

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT, Argentina) projects (PICT 2007–1114, PICT 2007–1119). Authors are members of CONICET (Argentina). Dr. Donald F. Haggerty, a retired career investigator and native English speaker, edited the final version of the manuscript.

Compliance with Ethics Requirements

Conflict of Interest

M. C. Orsini Delgado declares that she has no conflict of interest.

M. Galleano declares that she has no conflict of interest.

M. C. Añón declares that she has no conflict of interest.

V. Tironi declares that she has no conflict of interest.

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

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Valeria A. Tironi.

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM 1

AAPH-derived radicals scavenging with preparations I (●), Id (○), H (▲) and Hd (∆). Panel a: the ORAC assay; Panel b: the ESR assay. (DOC 1520 kb)

ESM 2

Typical ESR spectra obtained for Panel a: PBN-adduct of AAPH-derived radicals, Panel b: DMPO-OH adduct. (DOC 457 kb)

ESM 3

Hydroxyl radicals inhibition with preparations I (●), Id (○), H (▲) and Hd (∆). Panel a: the HORAC assay; Panel b: the ESR assay. (DOC 1061 kb)

ESM 4

Scavenging % with preparations I (●), Id (○), H (▲), Hd (∆). Panel a: superoxide, Panel b: nitric oxide (DOC 338 kb)

ESM 5

Peroxynitrites scavenging with preparations I (●), Id (○), H (▲) and Hd (∆). (DOC 472 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Delgado, M.C.O., Galleano, M., Añón, M.C. et al. Amaranth Peptides from Simulated Gastrointestinal Digestion: Antioxidant Activity Against Reactive Species. Plant Foods Hum Nutr 70, 27–34 (2015). https://doi.org/10.1007/s11130-014-0457-2

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11130-014-0457-2

Keywords

Navigation