Cardiovascular diseases, including cardiomyopathy, are the major complications in diabetes. A deeper understanding of the molecular mechanisms leading to cardiomyopathy is critical for developing novel therapies. We proposed phosphoinositide3-kinase gamma (PI3Kγ) as a molecular target against diabetic cardiomyopathy, given the role of PI3Kγ in cardiac remodeling to pressure overload. Given the availability of a pharmacological inhibitor of this molecular target GE21, we tested the validity of our hypothesis by inducing diabetes in mice with genetic ablation of PI3Kγ or knock-in for a catalytically inactive PI3Kγ.
PI3Kγ Inhibition Protects Against Diabetic Cardiomyopathy in Mice / Maffei, Angelo; Cifelli, Giuseppe; Carnevale, Raimondo; Iacobucci, Roberta; Pallante, Fabio; Fardella, Valentina; Fardella, Stefania; Hirsch, Emilio; Lembo, Giuseppe; Carnevale, Daniela. - In: REVISTA ESPAÑOLA DE CARDIOLOGÍA. - ISSN 1885-5857. - (2017). [10.1016/j.rec.2016.04.034]
PI3Kγ Inhibition Protects Against Diabetic Cardiomyopathy in Mice
LEMBO, Giuseppe;CARNEVALE, DANIELA
2017
Abstract
Cardiovascular diseases, including cardiomyopathy, are the major complications in diabetes. A deeper understanding of the molecular mechanisms leading to cardiomyopathy is critical for developing novel therapies. We proposed phosphoinositide3-kinase gamma (PI3Kγ) as a molecular target against diabetic cardiomyopathy, given the role of PI3Kγ in cardiac remodeling to pressure overload. Given the availability of a pharmacological inhibitor of this molecular target GE21, we tested the validity of our hypothesis by inducing diabetes in mice with genetic ablation of PI3Kγ or knock-in for a catalytically inactive PI3Kγ.File | Dimensione | Formato | |
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Maffei_PI3K-Inhibition_2016.pdf
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