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成年猪心脏的体外复苏

Ex vivo resuscitation of adult pig hearts.

作者信息

Rosenstrauch Doreen, Akay Hakan M, Bolukoglu Hakki, Behrens Lars, Bryant Laura, Herrera Peter, Eya Kazuhiro, Tuzun Egemen, Clubb Fred J, Radovancevic Branislav, Frazier O H, Kadipasaoglu Kamuran A

机构信息

Cullen Cardiovascular Research Laboratories, Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, Texas 77030, USA.

出版信息

Tex Heart Inst J. 2003;30(2):121-7.

PMID:12809253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC161897/
Abstract

One possible way to expand the human heart donor pool is to include non-heart-beating human donors. To begin validating this approach, we developed an ex vivo cardiac perfusion circuit to support large mammalian hearts in Langendorff mode and beating-ejecting mode and to assess and improve their ischemic tolerance. In vivo hemodynamic data and heparinized blood (4.0 +/- 0.5 L) were collected from 6 anesthetized pigs. Hearts were isolated and connected to a recirculating perfusion circuit primed with autologous buffered blood (pH, 7.40). After retrograde aortic perfusion in Langendorff mode, the left atrium was gravity-filled at 10-20 mmHg, and the left ventricle began to eject against a compliance chamber in series with a systemic reservoir set to a hydraulic afterload of 100-120 mmHg. Left ventricular function was restored and maintained in all 6 hearts for 30 min. Cardiac output, myocardial oxygen consumption, stroke work, aortic pressure, left atrial pressure, and heart rate were measured. The mean myocardial oxygen consumption was 4.8 +/- 2.7 mL/min/100 g (95.8% of in vivo value); and mean stroke work, 5.3 +/- 1.1 g x m/100 g (58.95% of in vivo value). One resuscitated heart was exposed to 30 min of normothermic ischemic arrest, then flushed with Celsior and re-resuscitated. The ex vivo perfusion method described herein restored left ventricular ejection function and allowed assessment of ischemic tolerance in large mammalian hearts, potentially a 1st step toward including non-heart-beating human donors in the human donor pool.

摘要

扩大人类心脏供体库的一种可能方法是纳入非心脏跳动的人类供体。为了开始验证这种方法,我们开发了一种体外心脏灌注回路,以在Langendorff模式和跳动-射血模式下支持大型哺乳动物心脏,并评估和提高其缺血耐受性。从6只麻醉猪身上收集体内血流动力学数据和肝素化血液(4.0±0.5升)。分离心脏并连接到用自体缓冲血液(pH值7.40)预充的循环灌注回路。在Langendorff模式下进行逆行主动脉灌注后,左心房在10-20 mmHg压力下重力充盈,左心室开始对着与设置为100-120 mmHg液压后负荷的体循环储液器串联的顺应性腔室射血。所有6颗心脏的左心室功能均恢复并维持30分钟。测量心输出量、心肌耗氧量、每搏功、主动脉压力、左心房压力和心率。平均心肌耗氧量为4.8±2.7 mL/min/100 g(为体内值的95.8%);平均每搏功为5.3±1.1 g·m/100 g(为体内值的58.95%)。一颗复苏的心脏经历30分钟的常温缺血性停搏,然后用Celsior冲洗并再次复苏。本文所述的体外灌注方法恢复了左心室射血功能,并允许评估大型哺乳动物心脏的缺血耐受性,这可能是将非心脏跳动的人类供体纳入人类供体库的第一步。

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Transplantation of Hearts Donated after Circulatory Death.循环性死亡后捐献心脏的移植
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本文引用的文献

1
A comparative study of Celsior and University of Wisconsin solutions based on 12-hr preservation followed by transplantation in canine models.基于在犬类模型中进行12小时保存后移植,对赛而斯欧液和威斯康星大学溶液的一项比较研究。
J Heart Lung Transplant. 1999 Dec;18(12):1202-10. doi: 10.1016/s1053-2498(99)00092-3.
2
Successful orthotopic pig heart transplantation from non-heart-beating donors.非心脏跳动供体原位猪心脏移植成功。
J Heart Lung Transplant. 1999 Jun;18(6):597-606. doi: 10.1016/s1053-2498(98)00017-5.
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Transplantation. 1996 Sep 27;62(6):729-34. doi: 10.1097/00007890-199609270-00005.
4
Coenzyme Q10 protects coronary endothelial function from ischemia reperfusion injury via an antioxidant effect.辅酶Q10通过抗氧化作用保护冠状动脉内皮功能免受缺血再灌注损伤。
Surgery. 1996 Aug;120(2):189-96. doi: 10.1016/s0039-6060(96)80287-x.
5
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J Surg Res. 1996 Jun;63(1):220-4. doi: 10.1006/jsre.1996.0251.
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Tex Heart Inst J. 1993;20(1):33-9.
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The contribution of endothelial cells to hyperacute rejection in xenogeneic perfused working hearts.内皮细胞在异种灌注工作心脏超急性排斥反应中的作用。
Transplantation. 1994 Jan;57(2):262-7. doi: 10.1097/00007890-199401001-00019.
8
Lack of successful reanimation of pig hearts harvested more than 10 minutes after death.对死后超过10分钟摘取的猪心脏进行复苏未获成功。
J Heart Lung Transplant. 1995 Mar-Apr;14(2):322-8.
9
Categories of non-heart-beating donors.非心脏跳动供体的类别。
Transplant Proc. 1995 Oct;27(5):2893-4.
10
Oxygen consumption in rabbit Langendorff hearts perfused with a saline medium.用盐溶液灌注的兔离体心脏的耗氧量。
Acta Physiol Scand. 1981 Sep;113(1):117-22. doi: 10.1111/j.1748-1716.1981.tb06870.x.