Inhibition of the formation of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethyl-3H-imidazo[4,5-f]quinoxaline (MeIQx) by phenolics in model systems and beef patties

The comparative inhibition of the formation of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethyl-3H-imidazo[4,5-f]quinoxaline (MeIQx) by phenolics in both model systems and beef patties was studied to better understand the protective role of these compounds. Model syste...

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Detalhes bibliográficos
Autores: Caro-Cabarcas, Angye D., Alcón, Esmeralda, Mariotti-Cellis, María Salomé, Pedreschi, Franco, Hidalgo, Francisco J., Zamora, Rosario
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2025
País:España
Recursos:Consejo Superior de Investigaciones Científicas (CSIC)
Repositório:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/402701
Acesso em linha:http://hdl.handle.net/10261/402701
https://api.elsevier.com/content/abstract/scopus_id/105001475943
Access Level:Acceso aberto
Palavra-chave:Acrolein (PubChem ID: 7847)
Carbonyl-amine reactions
Carbonyl-phenol reactions
Food carbonylome
Heterocyclic aromatic amines
Maillard reaction
MeIQx (PubChem ID: 62275)
PhIP (PubChem ID: 1530)
Phenylacetaldehyde (PubChem ID: 998)
Phenylalanine (PubChem ID: 6140)
Reactive carbonyls
Threonine (PubChem ID: 6288)
Descrição
Resumo:The comparative inhibition of the formation of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethyl-3H-imidazo[4,5-f]quinoxaline (MeIQx) by phenolics in both model systems and beef patties was studied to better understand the protective role of these compounds. Model systems were selected to produce PhIP and MeIQx by carbonyl-amine reactions. Obtained results showed that their formation was inhibited up to 100 % by assayed phenolics. Among simple phenolics, m-diphenols were usually more effective than o-diphenols, and MeIQx was better inhibited than PhIP because m-diphenols both produce the Strecker degradation of amino acids to a lower extent than o-diphenols, and trap acrolein (responsible for MeIQx formation) better than phenylacetaldehyde (responsible for PhIP formation). When complex phenolics were assayed, other groups also contributed to the observed protective function. However, relative inhibitions of both compounds in model systems and beef patties were correlated, therefore suggesting that the formation of PhIP and MeIQx also occurs in beef patties by carbonyl-amine reactions.