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1.
Food Res Int ; 105: 210-220, 2018 03.
Article in English | MEDLINE | ID: mdl-29433209

ABSTRACT

Addition of ß-acids extracted from hop at different levels (0, 30mgkg-1, 60mgkg-1, 240mgkg-1) to the diet of broiler chickens demonstrated significant effects on the average concentration of polar metabolites and fatty acids of relevance for meat quality. The largest metabolic differences between control group and chicken fed different levels of ß-acids were achieved using 30mgkg-1 of supplement. As determined by EPR spin-trapping, increased redox stability was also obtained for meat from chicken fed 30mgkg-1 of ß-acids which also had highest level of endogenous antioxidants, especially anserine, carnosine, NADH and PUFAs. Diet and storage period were found to affect protein oxidation and myosin and actin were recognized as the main targets of protein oxidation. Myofibrillar proteins from chicken fed hop ß-acids showed to be less susceptible to oxidation. A moderated level of hop ß-acids as dietary supplement accordingly improve the overall redox stability, protecting myofibrillar proteins and fatty acids against oxidation and improve the nutritional properties of meat from broiler chickens.


Subject(s)
Animal Feed , Chickens , Humulus/chemistry , Meat/analysis , Terpenes/chemistry , Animals , Cyclohexanones/chemistry , Cyclohexanones/metabolism , Metabolome , Muscle Proteins/analysis , Muscle Proteins/chemistry , Oxidation-Reduction , Terpenes/metabolism
2.
Free Radic Res ; 49(1): 102-11, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25363553

ABSTRACT

Astaxanthin when esterified with ferulic acid is better singlet oxygen quencher with k2 = (1.58 ± 0.1) 10(10) L mol(-1)s(-1) in ethanol at 25°C compared with astaxanthin with k2 = (1.12 ± 0.01) 10(9) L mol(-1)s(-1). The ferulate moiety in the astaxanthin diester is a better radical scavenger than free ferulic acid as seen from the rate constant of scavenging of 1-hydroxyethyl radicals in ethanol at 25°C with a second-order rate constant of (1.68 ± 0.1) 10(8) L mol(-1)s(-1) compared with (1.60 ± 0.03) 10(7) L mol(-1)s(-1) for the astaxanthin:ferulic acid mixture, 1:2 equivalents. The mutual enhancement of antioxidant activity for the newly synthetized astaxanthin diferulate becoming a bifunctional antioxidant is rationalized according to a two-dimensional classification plot for electron donation and electron acceptance capability.


Subject(s)
Antioxidants/chemistry , Antioxidants/pharmacology , Antioxidants/chemical synthesis , Carotenoids/chemistry , Coumaric Acids/chemistry , Coumaric Acids/pharmacology , Oxidation-Reduction , Oxidative Stress , Xanthophylls/chemical synthesis , Xanthophylls/chemistry , Xanthophylls/pharmacology
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