Prevention of in vitro oxidation of low density lipoproteins (LDL) by amaranth peptides released by gastrointestinal digestion

The objective of this work was to analyze the capacity of amaranth peptides generated by gastrointestinal digestion to prevent LDL oxidation. A simulated gastrointestinal digest from protein isolate (Id); Id fractions separated by gel filtration FPLC, and synthetic peptides (products of digestion) w...

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Detalles Bibliográficos
Autores: García Fillería, Susan Fiorella, Tironi, Valeria Anahi
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/57197
Acceso en línea:http://hdl.handle.net/11336/57197
Access Level:acceso abierto
Palabra clave:Amaranth Proteins
Gastrointestinal Digestion
Ldl Oxidation
Peptides
https://purl.org/becyt/ford/2.11
https://purl.org/becyt/ford/2
Descripción
Sumario:The objective of this work was to analyze the capacity of amaranth peptides generated by gastrointestinal digestion to prevent LDL oxidation. A simulated gastrointestinal digest from protein isolate (Id); Id fractions separated by gel filtration FPLC, and synthetic peptides (products of digestion) were evaluated. The evolution of conjugated dienes (CD) and, for most active samples, TBARS, fluorescent compounds (FC) evolution and electrophoretic mobility (EM) during Cu+2/H2O2-induced-LDL-oxidation were evaluated. Id was able to increase the lag time and to decrease the propagation rate for CD and FC formation; however, EM was not modified. Most active FPLC fractions (0.59–1.4 kDa) attained a complete inhibition of CD, and partial or total prevention of FC formation and electrophoretic changes. Peptides evaluation indicated that the presence of histidine, hydrophobic and aromatic residues would be important in the inhibition of Cu+2/H2O2-induced LDL oxidation. The most active were cationic or neutral peptides.