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Abstract:

Some late complications of diabetes are associated with alterations in the structure and function of proteins due to glycation and free radicals generation. Aspirin inhibits protein glycation by acetylation of free amino groups. In the diabetic status, it was demonstrated that several enzymes of heme pathway were diminished. The aim of this work has been to investigate the in vivo effect of short and long term treatment with acetylsalicylic acid in streptozotocin induced diabetic mice. In both treatments, the acetylsalicylic acid prevented δ-aminolevulinic dehydratase and porphobilinogen deaminase inactivation in diabetic mice and blocked the accumulation of lipoperoxidative aldehydes. Catalase activity was significantly augmented in diabetic mice and the long term treatment with aspirin partially reverted it. We propose that oxidative stress might play an important role in streptozotocin induced diabetes. Our results suggest that aspirin can prevent some of the late complications of diabetes, lowering glucose concentration and probably inhibiting glycation by acetylation of protein amino groups. Copyright (C) 2000 Elsevier Science Ireland Ltd.

Registro:

Documento: Artículo
Título:Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition
Autor:Caballero, F.; Gerez, E.; Batlle, A.; Vazquez, E.
Filiación:Department of Biological Chemistry, FCEN, Univ. Buenos Aires, Ctro. I., Buenos Aires, Argentina
Palabras clave:Acetylsalicylic acid; Experimental diabetes mellitus; Glycation; Heme enzymes inactivation; Lipid peroxidation; Oxidative stress; acetylsalicylic acid; catalase; glucose; heme; porphobilinogen deaminase; porphobilinogen synthase; animal experiment; animal model; animal tissue; article; controlled study; enzyme activity; enzyme inactivation; glycation; lipid peroxidation; liver; male; mouse; nonhuman; oxidative stress; protein glycosylation; streptozocin diabetes; Animals; Aspirin; Blood Glucose; Catalase; Diabetes Mellitus, Experimental; Diet; Eating; Enzyme Inhibitors; Hemoglobin A, Glycosylated; Hydroxymethylbilane Synthase; Lipid Peroxidation; Male; Mice; Oxidative Stress; Porphobilinogen Synthase; Streptozocin
Año:2000
Volumen:126
Número:3
Página de inicio:215
Página de fin:225
DOI: http://dx.doi.org/10.1016/S0009-2797(00)00168-X
Título revista:Chemico-Biological Interactions
Título revista abreviado:Chem.-Biol. Interact.
ISSN:00092797
CODEN:CBINA
CAS:Aspirin, 50-78-2; Blood Glucose; Catalase, EC 1.11.1.6; Enzyme Inhibitors; Hemoglobin A, Glycosylated; Hydroxymethylbilane Synthase, EC 2.5.1.61; Porphobilinogen Synthase, EC 4.2.1.24; Streptozocin, 18883-66-4
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00092797_v126_n3_p215_Caballero

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Citas:

---------- APA ----------
Caballero, F., Gerez, E., Batlle, A. & Vazquez, E. (2000) . Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition. Chemico-Biological Interactions, 126(3), 215-225.
http://dx.doi.org/10.1016/S0009-2797(00)00168-X
---------- CHICAGO ----------
Caballero, F., Gerez, E., Batlle, A., Vazquez, E. "Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition" . Chemico-Biological Interactions 126, no. 3 (2000) : 215-225.
http://dx.doi.org/10.1016/S0009-2797(00)00168-X
---------- MLA ----------
Caballero, F., Gerez, E., Batlle, A., Vazquez, E. "Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition" . Chemico-Biological Interactions, vol. 126, no. 3, 2000, pp. 215-225.
http://dx.doi.org/10.1016/S0009-2797(00)00168-X
---------- VANCOUVER ----------
Caballero, F., Gerez, E., Batlle, A., Vazquez, E. Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition. Chem.-Biol. Interact. 2000;126(3):215-225.
http://dx.doi.org/10.1016/S0009-2797(00)00168-X