TY - JOUR
T1 - Poly(ADP-ribose) polymerase inhibition attenuates biventricular reperfusion injury after orthotopic heart transplantation
AU - Szabó, Gábor
AU - Soós, Pál
AU - Heger, Ulrike
AU - Flechtenmacher, Christa
AU - Bährle, Susanne
AU - Zsengellér, Zsuzsanna
AU - Szabó, Csaba
AU - Hagl, Siegfried
PY - 2005/2
Y1 - 2005/2
N2 - Objective: Poly (ADP-ribose) polymerase (PARP) activation plays a key role in free radical induced injury in ischemia/reperfusion. We investigated the effects of INO-1001 a novel PARP inhibitor on postischemic myocardial and endothelial function. Methods: In dogs, 12 orthotopic heart transplantations were performed after 4 h ischemic preservation. At the beginning of reperfusion either saline vehicle (control, n=6), or INO-1001 (1 mg/kg, n=6) was applied. Before explantation and after 120 min of reperfusion we measured biventricular pressure-volume relationships by a combined conductance catheter and the adaptation potential of the right ventricle to acute afterload increase by pulmonary banding. Coronary blood flow (CBF), vasoreactivity, PARP-activation and ATP-content were also determined. Results: INO-1001 led to significantly better recovery of contractility (91±3 vs. 44±7%, P<0.05) and CBF (44±4 vs. 29±3 ml/min, P<0.05) and higher increase in CBF after acetylcholine (61±10 vs. 27±8%, P<0.05). In addition, the inotropic adaptation potential of the right ventricle to an increased afterload was better preserved after INO-1001. ATP content was significantly higher in the INO-1001 group (11.0±2.1 vs. 4.5±1.1 μmol/g drw). Immunhistology revealed PARP activation in the control group which was abolished by INO-1001 treatment. Conclusions: PARP inhibition reduces myocardial and endothelial reperfusion injury after orthotopic heart transplantation.
AB - Objective: Poly (ADP-ribose) polymerase (PARP) activation plays a key role in free radical induced injury in ischemia/reperfusion. We investigated the effects of INO-1001 a novel PARP inhibitor on postischemic myocardial and endothelial function. Methods: In dogs, 12 orthotopic heart transplantations were performed after 4 h ischemic preservation. At the beginning of reperfusion either saline vehicle (control, n=6), or INO-1001 (1 mg/kg, n=6) was applied. Before explantation and after 120 min of reperfusion we measured biventricular pressure-volume relationships by a combined conductance catheter and the adaptation potential of the right ventricle to acute afterload increase by pulmonary banding. Coronary blood flow (CBF), vasoreactivity, PARP-activation and ATP-content were also determined. Results: INO-1001 led to significantly better recovery of contractility (91±3 vs. 44±7%, P<0.05) and CBF (44±4 vs. 29±3 ml/min, P<0.05) and higher increase in CBF after acetylcholine (61±10 vs. 27±8%, P<0.05). In addition, the inotropic adaptation potential of the right ventricle to an increased afterload was better preserved after INO-1001. ATP content was significantly higher in the INO-1001 group (11.0±2.1 vs. 4.5±1.1 μmol/g drw). Immunhistology revealed PARP activation in the control group which was abolished by INO-1001 treatment. Conclusions: PARP inhibition reduces myocardial and endothelial reperfusion injury after orthotopic heart transplantation.
KW - Heart transplantation
KW - PARP
KW - Reperfusion
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U2 - 10.1016/j.ejcts.2004.10.055
DO - 10.1016/j.ejcts.2004.10.055
M3 - Article
C2 - 15691675
AN - SCOPUS:13244278121
SN - 1010-7940
VL - 27
SP - 226
EP - 234
JO - European Journal of Cardio-thoracic Surgery
JF - European Journal of Cardio-thoracic Surgery
IS - 2
ER -