Intracoronary Stem Cell Delivery to the Right Ventricle: A Preclinical Study

Semin Thorac Cardiovasc Surg. 2016;28(4):817-824. doi: 10.1053/j.semtcvs.2016.10.003. Epub 2016 Oct 14.

Abstract

Clinical protocols for stem cell-based therapies are currently under development for patients with hypoplastic left heart syndrome. An ideal cell delivery method should have minimal safety risks and provide a wide distribution of cells to the nonischemic right ventricle (RV). However, the optimal strategy for stem cell delivery to the RV has yet to be explored in a preclinical model, necessary for a hypoplastic left heart syndrome trial. Human c-kit+ cardiac stem cells (CSCs) were delivered to healthy Yorkshire swine through the proximal right coronary artery with a stop and reflow technique. The effect of premedication with antiarrhythmic (AA) medications in this model was retrospectively reviewed, with the primary outcome of survival 2 hours after infusion. A group underwent CSC delivery to the RV without prophylactic AA medication (no AA, n = 7), whereas the second group was premedicated with a loading dose and intravenous infusion of amiodarone and lidocaine (AA, n = 13). Cardiac biopsies were obtained from each chamber to ascertain the biodistribution of CSCs. Survival was significantly greater in the prophylactic AA group compared with the group without AA (13/13 [100%] vs 1/7 [14.3%], P < 0.0001). Cardiac arrest during balloon inflation was the cause of death in each of the nonmedicated animals. In the premedicated group, 9 (69.2%) pigs experienced transient ST segment changes in the precordial leads during CSC delivery, which resolved spontaneously. Most c-kit+ CSCs were distributed to lateral segments of the RV free wall, consistent with the anatomical course of the right coronary artery (lateral RV, 19.2 ± 1.5 CSCs/field of view vs medial RV, 10.4 ± 1.3 CSCs/field of view, P < 0.0001). Few c-kit+ CSCs were identified in the right atrium, septum, or left ventricle. Prophylactic infusion of AA enhances survival in swine undergoing intracoronary delivery of human c-kit+ CSCs to the RV. Additionally, intracoronary delivery results in a limited biodistribution of c-kit+ CSCs within the RV. Human clinical protocols can be optimized by requiring infusion of AA medications before cell delivery.

Keywords: congenital heart disease; right ventricle; stem cell.

MeSH terms

  • Amiodarone / administration & dosage*
  • Animals
  • Anti-Arrhythmia Agents / administration & dosage*
  • Arrhythmias, Cardiac / etiology
  • Arrhythmias, Cardiac / physiopathology
  • Arrhythmias, Cardiac / prevention & control*
  • Biomarkers / metabolism
  • Cell Survival
  • Cells, Cultured
  • Female
  • Graft Survival
  • Heart Ventricles / metabolism
  • Heart Ventricles / pathology
  • Heart Ventricles / physiopathology
  • Heart Ventricles / surgery*
  • Heterografts
  • Humans
  • Lidocaine / administration & dosage*
  • Male
  • Models, Animal
  • Phenotype
  • Proto-Oncogene Proteins c-kit / metabolism
  • Retrospective Studies
  • Stem Cell Transplantation* / adverse effects
  • Stem Cell Transplantation* / methods
  • Stem Cells* / metabolism
  • Stem Cells* / pathology
  • Sus scrofa
  • Time Factors

Substances

  • Anti-Arrhythmia Agents
  • Biomarkers
  • Lidocaine
  • Proto-Oncogene Proteins c-kit
  • Amiodarone