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Fig.Ā 4 | Cardiovascular Diabetology

Fig.Ā 4

From: Irisin attenuates type 1 diabetic cardiomyopathy by anti-ferroptosisĀ via SIRT1-mediated deacetylation of p53

Fig.Ā 4

Erastin 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€‰=ā€‰6 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€‰=ā€‰50Ā Ī¼m; nā€‰=ā€‰6 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€‰=ā€‰500Ā nm; nā€‰=ā€‰6 per group). Data are presented as the meanā€‰Ā±ā€‰SD. One-way ANOVA, and Bonferroniā€™s post-hoc test. *Pā€‰<ā€‰0.05, **Pā€‰<ā€‰0.01. 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 microscopy

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