Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Bull Exp Biol Med ; 140(1): 41-3, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16254616

RESUMO

We measured the content of lipid peroxides in plasma LDL from patients with chronic CHD not accompanied by hypercholesterolemia; CHD and hypercholesterolemia; type 2 diabetes mellitus and decompensation of carbohydrate metabolism; and CHD, circulatory insufficiency, and type 2 diabetes mellitus (without hypercholesterolemia). The content of lipid peroxides in LDL isolated from blood plasma by differential ultracentrifugation in a density gradient was estimated by a highly specific method with modifications (reagent Fe(2+) xylene orange and triphenylphosphine as a reducing agent for organic peroxides). The content of lipid peroxides in LDL from patients was much higher than in controls (patients without coronary heart disease and diabetes). Hypercholesterolemia and diabetes can be considered as factors promoting LDL oxidation in vivo. Our results suggest that stimulation of lipid peroxidation in low-density lipoproteins during hypercholesterolemia and diabetes is associated with strong autooxidation of cholesterol and glucose during oxidative and carbonyl (aldehyde) stress, respectively. These data illustrate a possible mechanism of the progression of atherosclerosis in patients with diabetes mellitus.


Assuntos
Aterosclerose/metabolismo , Doença das Coronárias/metabolismo , Diabetes Mellitus Tipo 2/metabolismo , Hipercolesterolemia/metabolismo , Estresse Oxidativo/fisiologia , Adulto , Aterosclerose/complicações , LDL-Colesterol/sangue , LDL-Colesterol/metabolismo , Doença das Coronárias/complicações , Diabetes Mellitus Tipo 2/complicações , Feminino , Humanos , Hipercolesterolemia/complicações , Peróxidos Lipídicos/metabolismo , Masculino , Pessoa de Meia-Idade , Ultracentrifugação
2.
Ter Arkh ; 76(8): 10-5, 2004.
Artigo em Russo | MEDLINE | ID: mdl-15471387

RESUMO

AIM: To study an antioxidant action of antioxidant vitamins (vitamins C, E and provitamin A) in vitro and in vivo. MATERIAL AND METHODS: The study was made of kinetic parameters of copper-initiated free radical oxidation (FRO) of low density lipoproteins (HDLP) in human blood plasm, antioxidant potential of rat liver and myocardium, the level of FRO products in HDLP and activity of glutathione peroxidase in erythrocytes of 31 males aged 40-64 years with coronary heart disease (CHD). RESULTS: An antioxidant action of the combinations alpha-tocopherol+ascorbic acid and alpha-tocopherol+beta-carotin was much more potent than that of each of the component alone. The whole complex of the antioxidants completely suppressed FRO of HDLP in the model system. Feeding rats for 30 days with a complex of antioxidant vitamins and selenium produced a sharp enhancement of the antioxidant potential of the liver and a complete suppression of free radical processes in the myocardium. If this complex was given to CHD patients for 2 months, it sharply reduced the amount of FRO primary and secondary products in blood plasm LDLP in growing activity of erythrocytic selenium-containing glutathione peroxidase. CONCLUSION: The scheme is proposed for objective experimental assessment of antioxidant efficacy of multicomponent antioxidant medication in laboratory and clinical trials.


Assuntos
Antioxidantes/uso terapêutico , Doença das Coronárias/tratamento farmacológico , Coração/efeitos dos fármacos , Fígado/efeitos dos fármacos , Adulto , Animais , Antioxidantes/farmacologia , Ácido Ascórbico/farmacologia , Cobre/antagonistas & inibidores , Cobre/farmacologia , Doença das Coronárias/metabolismo , Combinação de Medicamentos , Radicais Livres/análise , Radicais Livres/metabolismo , Glutationa Peroxidase/sangue , Glutationa Peroxidase/metabolismo , Humanos , Lipoproteínas LDL/sangue , Lipoproteínas LDL/efeitos dos fármacos , Lipoproteínas LDL/metabolismo , Fígado/metabolismo , Masculino , Pessoa de Meia-Idade , Miocárdio/química , Miocárdio/metabolismo , Oxirredução , Ratos , Ratos Wistar , Vitamina E/farmacologia , Vitaminas/farmacologia , Vitaminas/uso terapêutico , beta Caroteno/farmacologia
3.
Bull Exp Biol Med ; 137(1): 20-3, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15085236

RESUMO

The severity of disturbances in carbohydrate metabolism in rats with alloxan-induced diabetes depended on activity of antioxidant enzymes in the target organ (pancreas). Damage to the pancreas is related to intensive generation of reactive oxygen species, free radicals, and lipid peroxides. Alloxan-induced diabetes in rats is a free radical disease, which in vivo serves as a useful model for the search for pharmacological preparations with antiradical and antioxidant properties. The antioxidant compound probucol indirectly increased activity of antioxidant enzymes in the pancreas and prevented the development of alloxan-induced diabetes in rats. Our results indicate that different sensitivity of laboratory animals of various species (rats and guinea pigs) to the influence of alloxan is associated with abnormal variations in activity of enzymes utilizing reactive oxygen species and lipid peroxides in mammalian pancreatic cells.


Assuntos
Antioxidantes/uso terapêutico , Diabetes Mellitus Experimental/enzimologia , Diabetes Mellitus Experimental/prevenção & controle , Ilhotas Pancreáticas/efeitos dos fármacos , Pâncreas/enzimologia , Probucol/uso terapêutico , Animais , Antioxidantes/farmacologia , Glutationa Peroxidase/análise , Glutationa Peroxidase/metabolismo , Glutationa Transferase/análise , Glutationa Transferase/metabolismo , Masculino , Estresse Oxidativo/efeitos dos fármacos , Pâncreas/química , Probucol/farmacologia , Ratos , Espécies Reativas de Oxigênio/farmacologia , Superóxido Dismutase/análise , Superóxido Dismutase/metabolismo
4.
Bull Exp Biol Med ; 136(2): 132-4, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-14631491

RESUMO

Glycosylation end-products formed during diabetes mellitus promoted atherogenic oxidative modification of low-density lipoproteins. We evaluated the effects of compensation of carbohydrate metabolism and therapy with antioxidant probucol on parameters of free radical oxidation in patients with type II diabetes mellitus. Compensation of carbohydrate metabolism reduced manifestations of oxidative stress, which was manifested in accelerated enzymatic utilization of reactive oxygen species and lipid peroxides and decreased content of free radical oxidation products in low-density lipoproteins. In patients with type II diabetes mellitus combination therapy with antioxidant probucol decreased the severity of oxidative stress and stabilized carbohydrate metabolism without increasing the dose of hypoglycemic preparations.


Assuntos
Metabolismo dos Carboidratos , Diabetes Mellitus Tipo 2/metabolismo , Estresse Oxidativo , Espécies Reativas de Oxigênio/metabolismo , Idoso , Antioxidantes/uso terapêutico , Diabetes Mellitus Tipo 2/tratamento farmacológico , Feminino , Hemoglobinas Glicadas/metabolismo , Humanos , Hipoglicemiantes/administração & dosagem , Hipoglicemiantes/uso terapêutico , Peroxidação de Lipídeos , Lipoproteínas LDL/sangue , Masculino , Malondialdeído/sangue , Pessoa de Meia-Idade , Oxirredução , Probucol/uso terapêutico
5.
Bull Exp Biol Med ; 136(2): 142-4, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-14631494

RESUMO

We studied the effect of a complex containing antioxidant vitamins C and E, provitamin A, and antioxidant element selenium on the contents of primary (lipid peroxides) and secondary products (malonic dialdehyde) of free radical lipid oxidation in low-density lipoproteins isolated from the plasma of patients with coronary heart disease and hypercholesterolemia by means of preparative ultracentrifugation. Activity of key antioxidant enzymes in the blood was measured during treatment with the antioxidant preparation. Combination treatment with antioxidant vitamins and antioxidant element selenium sharply decreased the contents of primary and secondary free radical oxidation products in circulating low-density lipoproteins and increased activity of antioxidant enzymes in erythrocytes. Activities of superoxide dismutase and selenium-containing glutathione peroxidase increased 1 and 2 months after the start of therapy, respectively.


Assuntos
Antioxidantes/metabolismo , Doença das Coronárias/metabolismo , Eritrócitos/enzimologia , Radicais Livres/metabolismo , Lipoproteínas LDL/metabolismo , Vitaminas/metabolismo , Adulto , Idoso , Antioxidantes/farmacologia , Catalase/sangue , Doença das Coronárias/tratamento farmacológico , Glutationa Peroxidase/sangue , Humanos , Peróxidos Lipídicos/metabolismo , Masculino , Malondialdeído/metabolismo , Pessoa de Meia-Idade , Oxirredução , Selênio/administração & dosagem , Selênio/metabolismo , Superóxido Dismutase/sangue , Vitaminas/farmacologia
6.
Bull Exp Biol Med ; 135(2): 143-6, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12802419

RESUMO

Antioxidant effect of a complex preparation including antioxidant vitamins C, E, provitamin A and selenium was studied on the model of Cu(2+)-initiated free-radical oxidation of LDL isolated from human blood plasma. The antioxidant effect of combined administration of alpha-tocopherol+ascorbic acid and alpha-tocopherol+beta-carotene is far more pronounced that the antioxidant effect of individual components of these cocktails. Moreover, in the model system the combined action of all antioxidant components completely inhibited free-radical oxidation of LDL. A 30-day course of peroral administration of antioxidant vitamin cocktail and selenium to rats pronouncedly enhanced the antioxidant potential of liver and completely suppressed free-radical processes in the myocardium. It is suggested that preparations containing antioxidant vitamins and selenium can be perspective for prevention and complex therapy of atherosclerosis.


Assuntos
Antioxidantes/metabolismo , Radicais Livres/metabolismo , Lipoproteínas LDL/metabolismo , Fígado/metabolismo , Miocárdio/metabolismo , Plasma/metabolismo , Vitaminas/metabolismo , Animais , Antioxidantes/administração & dosagem , Humanos , Fígado/citologia , Miocárdio/citologia , Oxirredução , Ratos , Selênio/metabolismo , Vitaminas/administração & dosagem , beta Caroteno/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...