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Oxid Med Cell Longev ; 2022: 9014155, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35464763

RESUMO

Diabetes mellitus (DM) is associated with mitochondrial dysfunction and oxidative stress that can lead to diabetic cardiomyopathy (DCM), which can often remain undetected until late stages of the disease. However, myocardial injury occurs before the onset of measurable cardiac dysfunction, although its molecular correlates are poorly understood. In this study, we made a DM rat induced by a high-fat diet combined with low and high doses of streptozotocin (STZ) to emulate pre and early DCM. RNA-sequencing analysis of ventricular tissue revealed a differential transcriptome profile and abnormal activation of pathways involved in fatty acid metabolism, oxidative phosphorylation, cardiac structure and function, insulin resistance, calcium signalling, apoptosis, and TNF signalling. Moreover, using high glucose-treated human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM), we recapitulated the cardiac cellular phenotype of DM and identified several molecular correlates that may promote the development of DCM. In conclusion, we have developed an experimental framework to target pathways underlying the progression of DCM.


Assuntos
Diabetes Mellitus Experimental , Cardiomiopatias Diabéticas , Células-Tronco Pluripotentes Induzidas , Animais , Apoptose , Diabetes Mellitus Experimental/tratamento farmacológico , Cardiomiopatias Diabéticas/metabolismo , Humanos , Células-Tronco Pluripotentes Induzidas/metabolismo , Miócitos Cardíacos/metabolismo , Estresse Oxidativo , Ratos , Estreptozocina/efeitos adversos
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