“…It should be noted that a relatively novel group of anti-diabetic agents, the SGLT2 inhibitors, have been shown to attenuate hyperglycemia-induced cardiac dysfunction in lipodystrophic mice[ 43 ]. In concordance, they exert a cardioprotective effect manifested by improved systolic function, decreased fibrosis and reduced inflammation in At II infusion-induced cardiomyopathy in diabetic mice[ 44 ], elucidating the beneficial effects of SGLT2 inhibitors observed in human studies[ 45 ]. Mechanisms by which SGLT2 inhibition mitigates DCM and HF in general is an increase in natriuresis, osmotic diuresis, plasma volume contraction, reduction of blood pressure and arterial stiffness and lastly, by providing highly energy-efficient substrates for cardiac metabolism, such as β-hydroxybutyrate[ 43 , 45 ].…”