Early changes in myocyte contractility and cardiac function in streptozotocin-induced type 1 diabetes in rats

Author(s)

Marchini, Gustavo S. ^[1] ; Cestari, Ismar N. ^[2] ; Salemi, Vera M. C. ^[2] ; Irigoyen, Maria Claudia ^[2] ; Arnold, Alexandre ^[2] ; Kakoi, Adelia ^[2] ; Rocon, Camila ^[2] ; Aiello, Vera D. ^[2] ; Cestari, Idagene A. ^{[2, 1]}

Affiliation

^[1] Univ Sao Paulo, Biomed Engn Grad Progam, Polytech Sch, Sao Paulo - Brazil

^[2] Univ Sao Paulo, Heart Inst InCor, Med Sch, Sao Paulo - Brazil

• Document type: Journal article
• Source: PLoS One; v. 15, n. 8 AUG 21 2020.
• Web of Science Citations: 0

Abstract

Diabetes can elicit direct deleterious effects on the myocardium, independent of coronary artery disease or hypertension. These cardiac disturbances are termed diabetic cardiomyopathy showing increased risk of heart failure with or without reduced ejection fraction. Presently, there is no specific treatment for this type of cardiomyopathy and in the case of type I diabetes, it may start in early childhood independent of glycemic control. We hypothesized that alterations in isolated myocyte contractility and cardiac function are present in the early stages of experimental diabetes in rats before overt changes in myocardium structure occur. Diabetes was induced by single-dose injection of streptozotocin (STZ) in rats with data collected from control and diabetic animals 3 weeks after injection. Left ventricle myocyte contractility was measured by single-cell length variation under electrical stimulation. Cardiac function and morphology were studied by high-resolution echocardiography with pulsed-wave tissue Doppler imaging (TDI) measurements and three-lead surface electrocardiogram. Triglycerides, cholesterol and liver enzyme levels were measured from plasma samples obtained from both groups. Myocardial collagen content and perivascular fibrosis of atria and ventricle were studied by histological analysis after picrosirius red staining. Diabetes resulted in altered contractility of isolated cardiac myocytes with increased contraction and relaxation time intervals. Echocardiography showed left atrium dilation, increased end-diastolic LV and posterior wall thickness, with reduced longitudinal systolic peak velocity (S') of the septum mitral annulus at the apical four-chamber view obtained by TDI. Triglycerides, aspartate aminotransferase and alkaline phosphatase were elevated in diabetic animals. Intertitial collagen content was higher in atria of both groups and did not differ among control and diabetic animals. Perivascular intramyocardial arterioles collagen did not differ between groups. These results suggest that alterations in cardiac function are present in the early phase in this model of diabetes type 1 and occur before overt changes in myocardium structure appear as evaluated by intersticial collagen deposition and perivascular fibrosis of intramyocardial arterioles. (AU)

• FAPESP's process: 12/50283-6 - Circulatory support in pediatric patients: ventricular assist device and extracorporeal membrane oxygenation
• Grantee: Idágene Aparecida Cestari
• Support Opportunities: Research Projects - Thematic Grants
• FAPESP's process: 13/24543-3 - Contractility changes in isolated cardiomyocytes following pediatric VAD support
• Grantee: Gustavo Shimabukuro Marchini
• Support Opportunities: Scholarships in Brazil - Doctorate (Direct)