miR-200a Attenuated Doxorubicin-Induced Cardiotoxicity through Upregulation of Nrf2 in Mice.
Model: Doxorubicin-induced cardiotoxicity; acute model using a single intraperitoneal injection of DOX-HCl at 15 mg/kg and chronic model using intraperitoneal DOX at 5 mg/kg weekly for four injections (cumulative dose 20 mg/kg)
miR-200a was decreased in doxorubicin-treated hearts. AAV9-mediated miR-200a overexpression restored cardiac miR-200a, blunted body weight loss, prevented the rise in cTnI and NT-proBNP, and preserved +dP/dt, ejection fraction and cardiac output after acute doxorubicin. It preserved the GSH/GSSG ra…
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