{"title":"非酶促褐变蛋白与脂质氧化产物反应的抗氧化活性","authors":"F. Hidalgo, M. Alaiz, R. Zamora","doi":"10.1533/9781845698447.6.225","DOIUrl":null,"url":null,"abstract":"Summary Three oxidized lipid/amino acid reaction (OLAARP): (1-methyl-4-pentyl-1,4-dihydropyridine-3,5-dicarbaldehyde, 1-(5′-amino-1′-carboxypentyl)pyrrole, and N -(carbobenzyloxy)-1(3)-(1′-(formyl(methyl)-hexyl)-L-histidine dehydrate), and two browned proteins (the monomer and the dimmer produced in the reaction between BSA and 4,5( E )-epoxy-2- E )-hepatenal) were prepared and tested for antioxidative activity in a microsomal system in order to investigate the antioxidative function of OLAARP and non-enzymatically browned proteins in biological systems. The microsomal sytem consisted fo freshly prepared trout muscle microsomes, which were oxidized with Cu 2+ , Fe 3+ /ascorbate, or Cu 2+ /H 2 O 2 at 37 °C and in the presence of the compound to be tested as antioxidant. The three OLAARP (tested at 50 μM) and the two browned proteins (tested at 40 μg/mL) efficiently protected against lipid peroxidation, assessed by the formation of thiobarbituric acid-reactive substances, and protein damage, determined by amino acid analysis. These results suggest that the formation of non-enzymatically browned proteins by reaction with lipid oxidation products may constitute an antioxidative defense mechanism, which could play a significant role in vivo .","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"16 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Antioxidative Activity of Non-Enzymatically Browned Proteins by Reaction with Lipid Oxidation Products\",\"authors\":\"F. Hidalgo, M. Alaiz, R. Zamora\",\"doi\":\"10.1533/9781845698447.6.225\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Summary Three oxidized lipid/amino acid reaction (OLAARP): (1-methyl-4-pentyl-1,4-dihydropyridine-3,5-dicarbaldehyde, 1-(5′-amino-1′-carboxypentyl)pyrrole, and N -(carbobenzyloxy)-1(3)-(1′-(formyl(methyl)-hexyl)-L-histidine dehydrate), and two browned proteins (the monomer and the dimmer produced in the reaction between BSA and 4,5( E )-epoxy-2- E )-hepatenal) were prepared and tested for antioxidative activity in a microsomal system in order to investigate the antioxidative function of OLAARP and non-enzymatically browned proteins in biological systems. The microsomal sytem consisted fo freshly prepared trout muscle microsomes, which were oxidized with Cu 2+ , Fe 3+ /ascorbate, or Cu 2+ /H 2 O 2 at 37 °C and in the presence of the compound to be tested as antioxidant. The three OLAARP (tested at 50 μM) and the two browned proteins (tested at 40 μg/mL) efficiently protected against lipid peroxidation, assessed by the formation of thiobarbituric acid-reactive substances, and protein damage, determined by amino acid analysis. These results suggest that the formation of non-enzymatically browned proteins by reaction with lipid oxidation products may constitute an antioxidative defense mechanism, which could play a significant role in vivo .\",\"PeriodicalId\":359473,\"journal\":{\"name\":\"The Maillard Reaction in Foods and Medicine\",\"volume\":\"16 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Maillard Reaction in Foods and Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1533/9781845698447.6.225\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Maillard Reaction in Foods and Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1533/9781845698447.6.225","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Antioxidative Activity of Non-Enzymatically Browned Proteins by Reaction with Lipid Oxidation Products
Summary Three oxidized lipid/amino acid reaction (OLAARP): (1-methyl-4-pentyl-1,4-dihydropyridine-3,5-dicarbaldehyde, 1-(5′-amino-1′-carboxypentyl)pyrrole, and N -(carbobenzyloxy)-1(3)-(1′-(formyl(methyl)-hexyl)-L-histidine dehydrate), and two browned proteins (the monomer and the dimmer produced in the reaction between BSA and 4,5( E )-epoxy-2- E )-hepatenal) were prepared and tested for antioxidative activity in a microsomal system in order to investigate the antioxidative function of OLAARP and non-enzymatically browned proteins in biological systems. The microsomal sytem consisted fo freshly prepared trout muscle microsomes, which were oxidized with Cu 2+ , Fe 3+ /ascorbate, or Cu 2+ /H 2 O 2 at 37 °C and in the presence of the compound to be tested as antioxidant. The three OLAARP (tested at 50 μM) and the two browned proteins (tested at 40 μg/mL) efficiently protected against lipid peroxidation, assessed by the formation of thiobarbituric acid-reactive substances, and protein damage, determined by amino acid analysis. These results suggest that the formation of non-enzymatically browned proteins by reaction with lipid oxidation products may constitute an antioxidative defense mechanism, which could play a significant role in vivo .