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Antioxidant, Angiotensin-Converting Enzyme Inhibitory Properties and Blood-Pressure-Lowering Effect of Rice Bran Protein Hydrolysates

dc.contributor.authorPiotrowicz, Inajara Beatriz Brose
dc.contributor.authorGarcés Rimón, Marta
dc.contributor.authorMoreno Fernández, Silvia
dc.contributor.authorAleixandre De Artiñano, María Amaya
dc.contributor.authorSalas Mellado, Myriam
dc.contributor.authorMiguel Castro, Marta
dc.date.accessioned2023-06-17T09:11:35Z
dc.date.available2023-06-17T09:11:35Z
dc.date.issued2020-06-20
dc.description.abstractThis research aimed to investigate the biological properties of different hydrolysates derived from industrial and laboratory defatted rice bran proteins. Industrial and laboratory defatted rice bran protein concentrates were hydrolyzed with alcalase or flavorzyme. The degree of hydrolysis (DH), oxygen radical absorbance capacity (ORAC), reducing power, total phenolic compounds (TPC), and angiotensin-converting enzyme (ACE) inhibitory activity, were determined in the hydrolysates and the molecular fractions lower than 3 kDa. Systolic blood pressure (SBP) was measured using the tail-cuff method before and after oral administration of 80 mg/kg of different rice bran protein hydrolysate (RBPH) fractions lower than 3 kDa in male spontaneously hypertensive rats (SHR) and normotensive Wistar–Kyoto (WKY) rats. The highest values of in vitro antioxidant activity and TPC were observed in RBPH with alcalase defatted by industry (RBPH2A), and, in all cases, these bioactivities were higher in the molecular fractions lower than 3 kDa. Once again, fractions lower than 3 kDa obtained with alcalase showed a potent ACE inhibitory activity (RBPH1A<3). The administration of RBPH1A<3 caused a significant decrease in the SBP in SHR, where the maximum decrease was reached at 8 h after administration. SBP in WKY rats was not modified after the administration of RBPH1A<3. These results suggest that the rice bran protein hydrolysates obtained from industry after treatment with alcalase could be an interesting source of bioactive peptides, with potential action on hypertension and other related pathologies.en
dc.description.departmentDepto. de Farmacología y Toxicología
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)/Fondo Europeo de Desarrollo Regional
dc.description.sponsorshipCoordinación de la Formación del Personal de Nivel Superior (Brasil)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/67523
dc.identifier.citationPiotrowicz, I. B. B., Garcés Rimón, M., Moreno Fernández, S. et al. «Antioxidant, Angiotensin-Converting Enzyme Inhibitory Properties and Blood-Pressure-Lowering Effect of Rice Bran Protein Hydrolysates». Foods, vol. 9, n.o 6, junio de 2020, p. 812. DOI.org (Crossref), https://doi.org/10.3390/foods9060812.
dc.identifier.doi10.3390/foods9060812
dc.identifier.issn2304-8158
dc.identifier.officialurlhttps://doi.org/10.3390/foods9060812
dc.identifier.relatedurlhttps://www.mdpi.com/2304-8158/9/6/812
dc.identifier.urihttps://hdl.handle.net/20.500.14352/8366
dc.issue.number6
dc.journal.titleFoods
dc.language.isoeng
dc.page.initial812
dc.publisherMDPI
dc.relation.projectIDAGL2017-89213
dc.relation.projectID99999.010839/2014-03
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordDefatted rice bran
dc.subject.keywordAntioxidant hydrolysates
dc.subject.keywordAntihypertensive activity
dc.subject.keywordBioactive compounds
dc.subject.keywordHypertensive rats
dc.subject.ucmDietética y nutrición (Medicina)
dc.subject.ucmFarmacología (Medicina)
dc.subject.ucmSistema cardiovascular
dc.subject.unesco3206 Ciencias de la Nutrición
dc.subject.unesco2411.03 Fisiología Cardiovascular
dc.titleAntioxidant, Angiotensin-Converting Enzyme Inhibitory Properties and Blood-Pressure-Lowering Effect of Rice Bran Protein Hydrolysatesen
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublication69e1c358-e1c6-40ee-9e03-e8b914f92d27
relation.isAuthorOfPublication.latestForDiscovery69e1c358-e1c6-40ee-9e03-e8b914f92d27

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