EL-Malkey, N., Michael, M., Ibrahim, M., Moawad, R., Abdul Rahman, M., Ebrahim, E. (2022). Comparative Protective and Therapeutic Effects of Folic Acid on Cardiac Electrical and Structural Changes in a Rat Model of Diabetic-Cardiomyopathy. Egyptian Journal of Histology, 45(4), 1049-1067. doi: 10.21608/ejh.2021.75755.1479
Naness Fouad EL-Malkey; Mariam Nasr Michael; Maher Nageb Ibrahim; Rania Said Moawad; Maha M. Ahmed Abdul Rahman; Ebtesam Mohamed Ebrahim. "Comparative Protective and Therapeutic Effects of Folic Acid on Cardiac Electrical and Structural Changes in a Rat Model of Diabetic-Cardiomyopathy". Egyptian Journal of Histology, 45, 4, 2022, 1049-1067. doi: 10.21608/ejh.2021.75755.1479
EL-Malkey, N., Michael, M., Ibrahim, M., Moawad, R., Abdul Rahman, M., Ebrahim, E. (2022). 'Comparative Protective and Therapeutic Effects of Folic Acid on Cardiac Electrical and Structural Changes in a Rat Model of Diabetic-Cardiomyopathy', Egyptian Journal of Histology, 45(4), pp. 1049-1067. doi: 10.21608/ejh.2021.75755.1479
EL-Malkey, N., Michael, M., Ibrahim, M., Moawad, R., Abdul Rahman, M., Ebrahim, E. Comparative Protective and Therapeutic Effects of Folic Acid on Cardiac Electrical and Structural Changes in a Rat Model of Diabetic-Cardiomyopathy. Egyptian Journal of Histology, 2022; 45(4): 1049-1067. doi: 10.21608/ejh.2021.75755.1479
Comparative Protective and Therapeutic Effects of Folic Acid on Cardiac Electrical and Structural Changes in a Rat Model of Diabetic-Cardiomyopathy
1Medical Physiology department, Faculty of medicine, Zagazig University Egypt
2anatomy and embryology
faculty of medicine zagazig university
3Human anatomy and Embryology, Faculty of medicine, Zagazig University Egypt
Abstract
Introduction: Diabetic cardiomyopathy (DCM) is a cardiac disorder that could progress to heart failure. There is conflicting data about the role of folic acid supplementation in treatment DCM. Aim of the Work: This study was performed to compare between the protective and therapeutic effects of folic acid on ECG and structural changes of DCM rat model. Materials and Methods: Sixty rats were divided as follows: Normal control groups (Ia and Ib), DCM groups (IIa and IIb): Fed high fat diet for 4 weeks then injected with streptozotocin (25 mg/kg/ i.p), and folic acid treated groups (IIIa and IIIb): rats received 5 mg/kg/day orally for 8 weeks from first day of confirmation of diabetes in rats in group (IIIa), and from the end of 7th week after confirmation of diabetes in rats in group (IIIb). ECG, blood pressure, lactate dehydrogenase, Creatine kinase-MB, soluble receptor of advanced glycation end products (sRAGE), oxidative stress (OS) and inflammatory markers were assessed. Histopathological analysis of left ventricular tissue using Hematoxylin & eosin, Masson’s Trichrome stains, and immunohistochemical analysis of Caspase3 and iNOS expression were performed. Results: A significant improvement in R wave amplitude, ST segment deviation and a reduction in sRAGE in folic acid protective not therapeutic group were found when compared to untreated DCM group. Moreover, cardiac enzymes, histopathological changes, collagen fiber deposition, oxidative stress (OS), inflammation, and apoptosis significantly improved in both folic acid treatment groups when compared to untreated DCM groups. Conclusion: The protective role of folic acid on cardiac injury in DCM rat model was more effective than the therapeutic ones that could be attributed to better glycemic, OS control and amelioration of AGE/RAGE signaling and improvement in cardiac structural changes.
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