1. The effects of exercise training on cardiac matrix metalloproteinases activity and cardiac function in mice with diabetic cardiomyopathy.
- Author
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Dede E, Liapis D, Davos C, Katsimpoulas M, Varela A, Mpotis I, Kostomitsopoulos N, and Kadoglou NPE
- Subjects
- Animals, Blood Glucose metabolism, Collagen genetics, Collagen metabolism, Diabetes Mellitus, Experimental chemically induced, Diabetes Mellitus, Experimental genetics, Diabetes Mellitus, Experimental physiopathology, Diabetic Cardiomyopathies chemically induced, Diabetic Cardiomyopathies genetics, Diabetic Cardiomyopathies physiopathology, Echocardiography, Elastin genetics, Elastin metabolism, Exercise Test, Extracellular Matrix genetics, Gene Expression Regulation, Heart Ventricles metabolism, Heart Ventricles physiopathology, Male, Matrix Metalloproteinase 9 metabolism, Mice, Mice, Inbred C57BL, Signal Transduction, Streptozocin administration & dosage, Tissue Inhibitor of Metalloproteinase-1 metabolism, Diabetes Mellitus, Experimental enzymology, Diabetic Cardiomyopathies enzymology, Extracellular Matrix enzymology, Matrix Metalloproteinase 9 genetics, Physical Conditioning, Animal physiology, Tissue Inhibitor of Metalloproteinase-1 genetics
- Abstract
Aim: To evaluate the effects of exercise training (ET) on cardiac extracellular matrix (ECM) proteins homeostasis and cardiac dysfunction in mice with diabetic cardiomyopathy., Methods: Thirty-six male C57BL/6 mice were randomized into 3 groups for 8 weeks (12mice/group): Diabetic control-DC: Diabetes was induced by single streptozotocin injection (200 mg/kg i.p.); Diabetic exercise-DE: Diabetic mice underwent ET program on motorized-treadmill (6-times/week, 60min/session); Non-diabetic control-NDC: Vehicle-treated, sedentary, non-diabetic mice served as controls. Before euthanasia, all groups underwent transthoracic echocardiography (TTE). Post-mortem, left-ventricle (LV) samples were histologically analysed for ECM proteins (collagen, elastin), matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs)., Results: DC group showed significantly higher cardiac contents of collagen and MMP-9 and lower elastic concentration than NDC (p < 0.001). The implementation of ET completely outweighed those diabetes-induced changes (DE vs NDC, p > 0.05). TIMP-1 levels significantly increased across all groups (DC: 18.98 ± 3.47%, DE: 24.24 ± 2.36%, NDC: 46.36 ± 5.91%; p < 0.05), while MMP-9/TIMP-1 ratio followed a reverse pattern. ET tended to increase MMP-2 concentrations versus DC (p = 0.055), but did not achieve non-diabetic levels (p < 0.05). TIMP-2 cardiac concentrations remained unaltered throughout the study (p > 0.05). Importantly, ET ameliorated both LV end-systolic internal diameter (LVESD) (p < 0.001) and the percentage of LV fractional shortening (FS%) (p = 0.006) compared to DC. Despite that favorable effect, the cardiac function level of DE group remained worse than NDC group (%FS: p = 0.002; LVESD: p < 0.001)., Conclusion: Systemic ET may favorably change ECM proteins, MMP-9 and TIMP-1 cardiac concentrations in mice with diabetic cardiomyopathy. Those results were associated with partial improvement of echocardiography-assessed cardiac function, indicating a therapeutic effect of ET in diabetic cardiomyopathy., Competing Interests: Declaration of competing interest The authors have no conflicts of interest to declare., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2022
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