Myoglobin-H(2)O(2) catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis


Autoria(s): GANINI, Douglas; CHRISTOFF, Marcelo; EHRENSHAFT, Marilyn; KADIISKA, Maria B.; MASON, Ronald P.; BECHARA, Etelvino J. H.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

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

http://dx.doi.org/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