Bone marrow mesenchymal stromal cells rescue cardiac function in streptozotocin-induced diabetic rats

Int J Cardiol. 2014 Feb 1;171(2):199-208. doi: 10.1016/j.ijcard.2013.12.013. Epub 2013 Dec 18.

Abstract

Objectives: In the present study, we investigated whether MSC-transplantation can revert cardiac dysfunction in streptozotocin-induced diabetic rats and the immunoregulatory effects of MSC were examined.

Background: Cardiac complications are one of the main causes of death in diabetes. Several studies have shown anti-diabetic effects of bone marrow mesenchymal stromal cells (MSC).

Methods/results: The rats were divided in three groups: Non-diabetic, Diabetic and Diabetic-Treated with 5 × 10(6) MSC 4 weeks after establishment of diabetes. Four weeks after MSC-therapy, systemic metabolic parameters, immunological profile and cardiac function were assessed. MSC-transplantation was able to revert the hyperglycemia and body weight loss of the animals. In addition, after MSC-transplantation a decrease in corticosterone and IFN-γ sera levels without restoration of insulin and leptin plasma levels was observed. Also, MSC-therapy improved electrical remodeling, shortening QT and QTc in the ECG and action potential duration of left ventricular myocytes. No arrhythmic events were observed after MSC-transplantation. MSC-therapy rescued the cardiac beta-adrenergic sensitivity by increasing beta-1 adrenergic receptor expression. Both alpha and beta cardiac AMPK and p-AMPK returned to baseline values after MSC-therapy. However, total ERK1 and p-ERK1/2 were not different among groups.

Conclusion: The results indicate that MSC-therapy was able to rescue cardiac impairment induced by diabetes, normalize cardiac AMPK subunit expression and activity, decrease corticosterone and glycemia and exert systemic immunoregulation.

Keywords: AMPK; Cardiac electrophysiology; Diabetes; Immunoregulation; Mesenchymal stromal cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Corticosterone / blood
  • Diabetes Complications / etiology
  • Diabetes Complications / immunology
  • Diabetes Complications / therapy*
  • Diabetes Mellitus, Experimental / complications*
  • Diabetes Mellitus, Experimental / immunology
  • Heart Conduction System / physiology
  • Heart Diseases / etiology
  • Heart Diseases / immunology
  • Heart Diseases / therapy*
  • Hyperglycemia / etiology
  • Hyperglycemia / immunology
  • Hyperglycemia / therapy*
  • Male
  • Mesenchymal Stem Cell Transplantation / methods*
  • Mesenchymal Stem Cells
  • Rats
  • Rats, Wistar
  • Signal Transduction / physiology
  • Ventricular Remodeling / physiology

Substances

  • Biomarkers
  • Blood Glucose
  • Corticosterone