2016
Moderate hypothermia during ex vivo machine perfusion promotes recovery of hearts donated after cardiocirculatory death
TOLBOOM, Herman; Veronika OLEJNÍČKOVÁ; Diana RESER; Barbara ROSSER; Markus J. WILHELM et al.Základní údaje
Originální název
Moderate hypothermia during ex vivo machine perfusion promotes recovery of hearts donated after cardiocirculatory death
Autoři
TOLBOOM, Herman; Veronika OLEJNÍČKOVÁ; Diana RESER; Barbara ROSSER; Markus J. WILHELM; Max GASSMANN; Anna BOGDANOVA a Volkmar FALK
Vydání
European Journal Cardio-Thoracic Surgery, Cary, Oxford University Press, 2016, 1010-7940
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.759
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/16:00089079
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Heart transplantation; Organ preservation; Machine perfusion; Declaration of cardiocirculatory death; Ischaemia-reperfusion
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 8. 2016 10:59, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
OBJECTIVES To establish the optimal machine perfusion temperature for recovery of hearts in a rodent model of donation after declaration of cardiocirculatory death (DCD). METHODS Hearts from male Lewis rats (n = 14/group) were subjected to 25 min of in situ warm (37°C) ischaemia to simulate DCD. They were then explanted and reperfused with diluted autologous blood for 60 min at 20, 25, 30, 33 or 37°C, after which they were stored at 0-4°C in Custodiol preservation solution for 240 min. Fresh-excised and cold-stored ischaemic hearts were used as controls. The viability of the different groups was assessed by comparing heart rate and left ventricular contractility in a Langendorff circuit, as well as perfusate levels of troponin-t and creatine kinase (CK), and myocardial levels of adenosine triphosphate (ATP) and reduced glutathione. RESULTS During ex vivo reperfusion, hearts in all groups resumed beating within minutes. The mean heart rate was highest in the 37°C group at 154.72 +/- 33.01 beats × min-1 (bpm), and declined in proportion to temperature to 39.72 +/- 5.53 bpm at 20°C. Troponin-t levels were highest in the 37°C group (79.49 +/- 20.79 µg/l), the values were significantly lower in all other reconditioned groups with a minimum of 12.472 +/- 7.08 µg/l in the 20°C group (P < 0.0001). Tissue ATP levels ranged from 4.32 ± 1.71 µmol/g at 33°C to 4.59 +/- 1.41 µmol/g at 30°C, all significantly higher than the mean ATP level of 1.41 +/- 0.93 µmol/g in untreated ischaemic hearts (P 0.0001). During Langendorff assessment, the mean heart rate and contractility of all groups were higher than those of cold-stored ischaemic hearts (P 0.0001), yet not significantly different from those of fresh controls. The perfusate levels of troponin-t and CK, and myocardial levels of reduced-glutathione and ATP were not significantly different between groups. CONCLUSION Our results suggest that mild hypothermia during ex vivo reperfusion improves recovery of ischaemic hearts in a rodent DCD model.