Fig.Ā 4From: Irisin attenuates type 1 diabetic cardiomyopathy by anti-ferroptosisĀ via SIRT1-mediated deacetylation of p53Erastin abolishes the protective effect of irisin on diabetic cardiomyopathy. Type 1 diabetic mice were treated with irisin (10Ā Ī¼g/kg body weight/day) in the presence or absence of the ferroptosis inducer erastin (40Ā mg/kg body weight/day, 3 consecutive days for 4Ā weeks). A1. Representative echocardiographic images from a mouse in each of the five groups of mice. Quantification of (A2) LVEF%, (A3) LVFS%, (A4) LVIDd, and (A5) LVIDs are shown (nā=ā6 per group). B Representative Masson staining images of heart tissues from a mouse in each of the five groups of mice: (B1) quantification (B2) of the fibrotic area (Scale barā=ā50Ā Ī¼m; nā=ā6 per group). C Representative TEM images from the heart of a mouse in each of the five groups of mice (C1) and corresponding relative Flameng scores (Bottom) (C2) of the mitochondria in myocardial tissues of each group (Scale barsā=ā500Ā nm; nā=ā6 per group). Data are presented as the meanāĀ±āSD. One-way ANOVA, and Bonferroniās post-hoc test. *Pā<ā0.05, **Pā<ā0.01. STZ streptozotocin, LVEF left ventricular ejection fraction, LVFS left ventricular fractional shortening, LVIDd left ventricular internal diameter at end-diastole, and LVIDs left ventricular internal diameter at end-systole, TEM transmission electron microscopyBack to article page