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1.
Med Sci Monit ; 12(7): RA130-47, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16810145

RESUMO

Diabetes mellitus has now assumed epidemic proportions in many countries of the world. With the present population of 19.4 million diabetics, and approximately 60 million by the year 2025, India would rank first in its share of the global burden of diabetes. Diabetes mellitus is characterized by derangement in carbohydrate, protein, and fat metabolism caused by complete or relative insufficiency of insulin secretion and/or insulin action. There are two main forms of diabetes, type 1 (insulin-dependent diabetes mellitus) and type 2 (non-insulin-dependent diabetes mellitus). Insulin sensitizers (thiazolidinediones), new-generation insulin secretagogue (glimepiride), acarbose, and designer insulin (lispro and aspart) have enormously helped in achieving better metabolic control. Despite the great strides that have been made in the understanding and management of type 2 diabetes, insulin resistance and diabetes-related complications are increasing unabated. The present review not only updates our knowledge in delineating the molecular mechanism(s) causal to insulin sensitivity or resistance, but also provides clues for the prognosis of diabetes and its better management.


Assuntos
Complicações do Diabetes , Consumo de Bebidas Alcoólicas , Complicações do Diabetes/dietoterapia , Complicações do Diabetes/tratamento farmacológico , Complicações do Diabetes/etiologia , Complicações do Diabetes/fisiopatologia , Humanos , Resistência à Insulina , Síndrome Metabólica/complicações , Síndrome Metabólica/terapia
2.
Acta Pharm ; 53(2): 91-100, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-14764243

RESUMO

Hepatoprotective activity of 3-bromo-6-(4-chlorophenyl)-4-methylthio-2H-pyran-2-one, an isostere of dimethyl ricinine, was evaluated in adult male albino rats intoxicated with carbon tetrachloride, paracetamol or thioacetamide. The test compound showed significant hepatoprotection at 6.0 mg kg(-1) body mass daily dose, given to the rats for seven consecutive days. The carbon tetrachloride, paracetamol and thioacetamide were given, respectively, on days 3, 5, and 7, on day 6 and on day 6 post treatment with the test compound. The protective effect was evident in a battery of serum and liver biochemical parameters related to hepatotoxicity.


Assuntos
Acetaminofen/toxicidade , Analgésicos não Narcóticos/toxicidade , Intoxicação por Tetracloreto de Carbono/prevenção & controle , Carcinógenos/toxicidade , Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Hidrocarbonetos Halogenados/uso terapêutico , Pironas/uso terapêutico , Tioacetamida/toxicidade , Animais , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Doença Hepática Induzida por Substâncias e Drogas/patologia , Colesterol/metabolismo , DNA/biossíntese , Fígado/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Testes de Função Hepática , Glicogênio Hepático/metabolismo , Masculino , Biossíntese de Proteínas , RNA/biossíntese , Ratos , Ratos Sprague-Dawley
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