Effects of intracoronary infusion of escalating doses of cardiac stem cells in rats with acute myocardial infarction

Academic Article

Abstract

  • © 2015 American Heart Association, Inc. Background-Although c-kitpos cardiac stem cells (CSCs) preserve left ventricular (LV) function and structure after myocardial infarction, CSC doses have been chosen arbitrarily, and the dose-effect relationship is unknown. Methods and Results-Rats underwent a 90-minute coronary occlusion followed by 35 days of reperfusion. Vehicle or CSCs at 5 escalating doses (0.3×106, 0.75×106, 1.5×106, 3.0×106, and 6.0×106 cells/heart) were given intracoronarily 4 h after reperfusion. The lowest dose (0.3×106) had no effect on LV function and morphology, whereas 0.75, 1.5, and 3.0×106 significantly improved regional and global LV function (echocardiography and hemodynamic studies). These 3 doses had similar effects on echocardiographic parameters (infarct wall thickening fraction, LV end-systolic and end-diastolic volumes, LV ejection fraction) and hemodynamic variables (LV end-diastolic pressure, LV dP/dtmax, preload adjusted maximal power, end-systolic elastance, preload recruitable stroke work) and produced similar reductions in apoptosis, scar size, infarct wall thinning, and LV expansion index and similar increases in viable myocardium in the risk region (morphometry). Infusion of 6.0×106 CSCs markedly increased postprocedural mortality. Green fluorescent protein and 5-bromo-2′-deoxyuridine staining indicated that persistence of donor cells and formation of new myocytes were negligible with all doses. Conclusions-Surprisingly, in this rat model of acute myocardial infarction, the dose-response relationship for intracoronary CSCs is flat. A minimal dose between 0.3 and 0.75×106 is necessary for efficacy; above this threshold, a 4-fold increase in cell number does not produce greater improvement in LV function or structure. Further increases in cell dose are harmful.
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    Author List

  • Tang XL; Rokosh G; Sanganalmath SK; Tokita Y; Keith MCL; Shirk G; Stowers H; Hunt GN; Wu W; Dawn B
  • Start Page

  • 757
  • End Page

  • 765
  • Volume

  • 8
  • Issue

  • 4