Myoglobin-H(2)O(2) catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2011
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Resumo |
Acetoacetate (AA) and 2-methylacetoacetate (MAA) are accumulated in metabolic disorders such as diabetes and isoleucinemia. Here we examine the mechanism of AA and MAA aerobic oxidation initiated by myoglobin (Mb)/H(2)O(2). We propose a chemiluminescent route involving a dioxetanone intermediate whose thermolysis yields triplet alpha-dicarbonyl species (methylglyoxal and diacetyl). The observed ultraweak chemiluminescence increased linearly on raising the concentration of either Mb (10-500 mu M) or AA (10-100 mM). Oxygen uptake studies revealed that MAA is almost a 100-fold more reactive than AA. EPR spin-trapping studies with MNP/MAA revealed the intermediacy of an alpha-carbon-centered radical and acetyl radical. The latter radical, probably derived from triplet diacetyl, is totally suppressed by sorbate, a well-known quencher of triplet carbonyls. Furthermore, an EPR signal assignable to MNP-AA(center dot) adduct was observed and confirmed by isotope effects. Oxygen consumption and a-dicarbonyl yield were shown to be dependent on AA or MAA concentrations (1-50 mM) and on H(2)O(2) or tert-butOOH added to the Mb-containing reaction mixtures. That ferrylMb is involved in a peroxidase cycle acting on the substrates is suggested by the reaction pH profiles and immunospin-trapping experiments. The generation of radicals and triplet dicarbonyl products by Mb/H(2)O(2)/beta-ketoacids may contribute to the adverse health effects of ketogenic unbalance. (C) 2011 Elsevier Inc. All rights reserved. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Instituto Nacional de Ciencia e Tecnologia (INCT) Redoxoma Instituto Nacional de Ciencia e Tecnologia (INCT) Redoxoma National Institute of Environmental Health Sciences (NIEHS/NIH) National Institute of Environmental Health Sciences (NIEHS/NIH) |
Identificador |
FREE RADICAL BIOLOGY AND MEDICINE, v.51, n.3, p.733-743, 2011 0891-5849 http://producao.usp.br/handle/BDPI/30988 10.1016/j.freeradbiomed.2011.05.002 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE INC |
Relação |
Free Radical Biology and Medicine |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE INC |
Palavras-Chave | #Myoglobin #Acetoacetate #2-Methylacetoacetate #Free radicals #Triplet carbonyls #Methylglyoxal #Diacetyl #Ketosis #GLYCATION END-PRODUCTS #CULTURED U937 MONOCYTES #TYPE-2 DIABETIC-NEPHROPATHY #HYDROGEN-PEROXIDE #HORSERADISH-PEROXIDASE #XYLENOL ORANGE #RENAL-FUNCTION #RAT MODEL #ACETOACETATE #METHYLGLYOXAL #Biochemistry & Molecular Biology #Endocrinology & Metabolism |
Tipo |
article original article publishedVersion |