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1.
J Cardiovasc Transl Res ; 3(5): 580-96, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20593256

RESUMO

Type 2 diabetes (T2DM) and its complications such as cardiomyopathy, contribute significantly to morbidity and mortality worldwide. Increased adoption of westernized diets and decreased physical activity are contributing to the obesity epidemic which, in turn, increases the risk for T2DM. Other risk factors for T2DM include insulin resistance, dyslipidemia, hypertension, metabolic syndrome, and a genetic predisposition. Risk measures for assessing these factors include family history, blood pressure, body weight, waist circumference, fasting glucose, insulin, and lipid levels, and calculated indices such as BMI, HOMA, and QUIKI. Most of these risk measures routinely done in annual check-ups, should help a primary care physician in making an early diagnosis of impending diabetic condition. The underlying mechanisms of these clinical, anthropometric and biochemical risk measures may also be involved in the etiology of diabetes and its complications. Their levels and changes over time therefore, may indeed reflect the disease process. Early and continued assessment of diabetes risk, as part of patient care, will help identify individuals most likely to develop diabetes and allow for early interventions to reduce risk factors as well as delay or may even prevent disease onset. In T2DM patients, ongoing measurement of risk markers and implementation of intervention where appropriate will improve the diabetic condition, decrease risk of cardiovascular and other complications, and decrease morbidity.


Assuntos
Cardiomiopatias/etiologia , Complicações do Diabetes/etiologia , Diabetes Mellitus Tipo 2/etiologia , Animais , Cardiomiopatias/prevenção & controle , Complicações do Diabetes/prevenção & controle , Diabetes Mellitus Tipo 2/diagnóstico , Diabetes Mellitus Tipo 2/prevenção & controle , Progressão da Doença , Dislipidemias/complicações , Diagnóstico Precoce , Feminino , Humanos , Hipertensão/complicações , Resistência à Insulina , Masculino , Obesidade/complicações , Valor Preditivo dos Testes , Prognóstico , Medição de Risco , Fatores de Risco , Fatores de Tempo , Resultado do Tratamento
2.
Biol Res ; 39(2): 307-19, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16874406

RESUMO

Type-1 5'-iodothyronine deiodinase (5'-DI) is responsible for conversion of T4 to T3. Selenium (Se) is an integral part of this enzyme. Keeping in view the strong association between atherosclerosis and hypothyroidism, the present study examined the behavior of 5'-DI in liver, aorta and thyroid during hypercholesterolemia following different Se status, i.e., Se deficiency (0.02 ppm), adequate (0.2 ppm) and excess dose (1 ppm) in SD male rats. Animals were fed a control or high-cholesterol diet (2%) for 1 and 2 months. 5'-DI activity and mRNA expression was measured by RIA and RT-PCR respectively. In liver and aorta, 5'-DI expression significantly decreased with the Se-deficient and the high-cholesterol diet. The trend was opposite in thyroid, i.e., mRNA expression increased significantly during selenium deficiency and with a high-cholesterol feeding. But with 1 ppm Se supplementation, the 5'-DI expression increased in all the three tissues. The present study indicates that hypercholesterolemia along with selenium deficiency is co-responsible for differential regulation of 5'-DI enzyme in thyroidal vs. extrathyroidal tissues. Distinct regulation of 5'-DI in the thyroid reflects the clinical importance of this selenoprotein during hypercholesterolemia as this enzyme is essential for T3 production, which further has a vital role in the maintenance of lipid metabolism.


Assuntos
Colesterol na Dieta/administração & dosagem , Hipercolesterolemia/metabolismo , Iodeto Peroxidase/metabolismo , RNA Mensageiro/metabolismo , Selênio/análise , Animais , Aorta/enzimologia , Colesterol na Dieta/metabolismo , Hipercolesterolemia/enzimologia , Iodeto Peroxidase/genética , Lipídeos/sangue , Fígado/enzimologia , Masculino , Radioimunoensaio , Ratos , Ratos Sprague-Dawley , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Selênio/metabolismo , Glândula Tireoide/enzimologia , Fatores de Tempo
3.
Biol. Res ; 39(2): 307-319, 2006. ilus, tab
Artigo em Inglês | LILACS | ID: lil-432433

RESUMO

Type-1 5'-iodothyronine deiodinase (5'-DI) is responsible for conversion of T4 to T3. Selenium (Se) is an integral part of this enzyme. Keeping in view the strong association between atherosclerosis and hypothyroidism, the present study examined the behavior of 5'-DI in liver, aorta and thyroid during hypercholesterolemia following different Se status, i.e., Se deficiency (0.02ppm), adequate (0.2ppm) and excess dose (1ppm) in SD male rats. Animals were fed a control or high-cholesterol diet (2%) for 1 and 2 months. 5'-DI activity and mRNA expression was measured by RIA and RT-PCR respectively. In liver and aorta, 5'-DI expression significantly decreased with the Se-deficient and the high-cholesterol diet. The trend was opposite in thyroid, i.e., mRNA expression increased significantly during selenium deficiency and with a high-cholesterol feeding. But with 1ppm Se supplementation, the 5'-DI expression increased in all the three tissues. The present study indicates that hypercholesterolemia along with selenium deficiency is co-responsible for differential regulation of 5'-DI enzyme in thyroidal vs. extrathyroidal tissues. Distinct regulation of 5'-DI in the thyroid reflects the clinical importance of this selenoprotein during hypercholesterolemia as this enzyme is essential for T3 production, which further has a vital role in the maintenance of lipid metabolism.


Assuntos
Animais , Masculino , Ratos , Colesterol na Dieta/administração & dosagem , Hipercolesterolemia/metabolismo , Iodeto Peroxidase/metabolismo , RNA Mensageiro/metabolismo , Selênio/análise , Aorta/enzimologia , Colesterol na Dieta/metabolismo , Hipercolesterolemia/enzimologia , Iodeto Peroxidase/genética , Lipídeos/sangue , Fígado/enzimologia , Radioimunoensaio , Ratos Sprague-Dawley , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Selênio/metabolismo , Fatores de Tempo , Glândula Tireoide/enzimologia
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