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J Cardiovasc Pharmacol Ther ; 25(1): 86-97, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31533469

RESUMO

BACKGROUND: Diabetic cardiomyopathy (DCM) is accompanied by microvascular complications that lead to myocardial dysfunction and heart failure. Most conventional therapies cannot ameliorate the microvascular insufficiency in DCM. In this study, we tested the hypothesis that undercarboxylated osteocalcin (ucOC) may be a new adjuvant therapy against the progression of DCM and its underlying microvascular pathology. MATERIALS AND METHODS: Diabetes was induced in Wistar rats with a high-fat diet combined with streptozotocin injections, and ucOC was upregulated after warfarin administration in the treated group. After 8 weeks, cardiac functions were assessed using a Langendorff apparatus. Cardiac tissue samples were also extracted to assess the ucOC receptor and vascular endothelial growth factor (VEGF) for histopathological studies. RESULTS: Both the systolic and the diastolic dysfunction observed in the DCM group were significantly improved after the increase in ucOC blood levels. Significant improvement in VEGF and CD31 expression after warfarin injection was associated with increased capillary density, neovascularization, and decreased myocardial fibrosis together with the reestablishment of myocardial structural and ultrastructural patterns. CONCLUSION: Undercarboxylated osteocalcin may have a promising effect in improving microvascular insufficiency and myocardial dysfunction in DCM.


Assuntos
Ácidos Carboxílicos/metabolismo , Circulação Coronária , Diabetes Mellitus Experimental/complicações , Cardiomiopatias Diabéticas/tratamento farmacológico , Cardiomiopatias Diabéticas/etiologia , Microcirculação , Miocárdio/metabolismo , Osteocalcina/metabolismo , Animais , Circulação Coronária/efeitos dos fármacos , Diabetes Mellitus Experimental/metabolismo , Cardiomiopatias Diabéticas/metabolismo , Cardiomiopatias Diabéticas/fisiopatologia , Fibrose , Preparação de Coração Isolado , Masculino , Microcirculação/efeitos dos fármacos , Miocárdio/ultraestrutura , Molécula-1 de Adesão Celular Endotelial a Plaquetas/metabolismo , Processamento de Proteína Pós-Traducional , Ratos Wistar , Transdução de Sinais , Regulação para Cima , Fator A de Crescimento do Endotélio Vascular/metabolismo , Remodelação Ventricular , Varfarina/farmacologia
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