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Mitochondrial transplantation for myocardial protection in ex-situ‒perfused hearts donated after circulatory death.

Authors :
Guariento A
Doulamis IP
Duignan T
Kido T
Regan WL
Saeed MY
Hoganson DM
Emani SM
Fynn-Thompson F
Matte GS
Del Nido PJ
McCully JD
Source :
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation [J Heart Lung Transplant] 2020 Nov; Vol. 39 (11), pp. 1279-1288. Date of Electronic Publication: 2020 Jun 29.
Publication Year :
2020

Abstract

Background: Donation after circulatory death (DCD) offers an additional source of cardiac allografts, potentially allowing expansion of the donor pool, but is limited owing to the effects of ischemia. In this study, we investigated the efficacy of mitochondrial transplantation to enhance myocardial function of DCD hearts.<br />Methods: Circulatory death was induced in Yorkshire pigs (40-50 kg, n = 29) by a cessation of mechanical ventilation. After 20 minutes of warm ischemia, cardioplegia was administered. The hearts were then reperfused on an ex-situ blood perfusion system. After 15 minutes of reperfusion, hearts received either vehicle alone (vehicle [VEH], 10 ml; n = 8) or vehicle containing autologous mitochondria (vehicle with mitochondria as a single injection [MT], 5 × 10 <superscript>9</superscript> in 10 ml, n = 8). Another group of hearts (serial injection of mitochondria [MT <subscript>S</subscript> ]; n = 6) received a second injection of mitochondria (5 × 10 <superscript>9</superscript> in 10 ml) after 2 hours of ex-situ heart perfusion and reperfused for an additional 2 hours. A Sham group (sham hearts; n = 6) did not undergo any warm ischemia.<br />Results: At the end of 4 hours of reperfusion, MT and MT <subscript>S</subscript> groups showed a significantly increased left ventricle/ventricular peak developed pressure (p = 0.002), maximal left ventricle/ventricular pressure rise (p < 0.001), fractional shortening (p < 0.001), and myocardial oxygen consumption (p = 0.004) compared with VEH. Infarct size was significantly decreased in MT and MT <subscript>S</subscript> groups compared with VEH (p < 0.001). No differences were found in arterial lactate levels among or within groups throughout reperfusion.<br />Conclusions: Mitochondrial transplantation significantly preserves myocardial function and oxygen consumption in DCD hearts, thus providing a possible option for expanding the heart donor pool.<br /> (Copyright © 2020 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1557-3117
Volume :
39
Issue :
11
Database :
MEDLINE
Journal :
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
Publication Type :
Academic Journal
Accession number :
32703639
Full Text :
https://doi.org/10.1016/j.healun.2020.06.023