Smolens I A, Follette D M, Berkoff H A, Castellanos L M, Segel L D
Division of Cardiothoracic Surgery, University of California, Davis, Medical Center, Sacramento, USA.
J Heart Lung Transplant. 1995 Sep-Oct;14(5):906-15.
This study was designed to determine the function of isolated rabbit hearts after static preservation with modified University of Wisconsin solution for 24 hours. Commercially available University of Wisconsin solution, modified with CaCl2 1 mmol/L and 2,3-butanedione monoxime 30 mmol/L, was used as the preservative. After flushing the coronary vasculature with medium, hearts were submersion stored at 1 degree C to 4 degrees C. After preservation, isolated heart function at 37 degrees C was quantified for 30 minutes in a non-ejecting mode and for 4 hours ejecting at a physiologic workload. Fresh control hearts (n = 5) and University of Wisconsin solution-preserved hearts (n = 6) were studied.
Nonworking (non-ejecting) left ventricular function of the two groups did not differ, except for peak rate of left ventricular pressure development which was higher for the University of Wisconsin solution hearts than for controls. When the hearts were subjected to a physiologic workload, however, left ventricular function of the two groups differed significantly. Three of the six University of Wisconsin solution hearts failed before the 4-hour perfusion end point, whereas all five control hearts maintained stable working function for the full 4 hours. The University of Wisconsin solution hearts, while in the ejecting mode, exhibited significantly impaired function. Mean values were as follows (p < 0.05): left ventricular systolic pressure (in millimeters of mercury), control 105 +/- 1, University of Wisconsin solution 86 +/- 4; peak rate of left ventricular pressure development (in millimeters of mercury per millisecond), control 3.33 +/- 0.11, University of Wisconsin solution 2.39 +/- 0.24; cardiac output (in milliliters per minute per gram), control 400 +/- 25, University of Wisconsin solution 288 +/- 26; stroke work (in milliJoules per gram), control 20.1 +/- 1.3, University of Wisconsin solution 11.9 +/- 1.1; left ventricular end-diastolic pressure (in millimeters of mercury), control 5.4 +/- 0.3, University of Wisconsin solution 10.2 +/- 1.3; peak aortic flow rate (in milliliters per minute), control 946 +/- 9, University of Wisconsin solution 659 +/- 44; millimoles of lactate produced in 30 min/Joule stroke work, control 0.50 +/- 0.06, University of Wisconsin solution 6.99 +/- 0.37.
These results indicate that (1) hypothermic storage in this modified University of Wisconsin solution does not preserve hearts sufficiently to support a physiologic workload for an extended period and (2) assessment of post-preservation function with a non-ejecting heart model does not accurately predict the ability of the preserved heart to support a physiologic workload.
本研究旨在确定用改良的威斯康星大学溶液静态保存24小时后离体兔心的功能。使用添加了1 mmol/L氯化钙和30 mmol/L 2,3 - 丁二酮单肟的市售威斯康星大学溶液作为防腐剂。用培养基冲洗冠状动脉血管后,心脏于1℃至4℃浸没保存。保存后,在37℃下对离体心脏功能进行30分钟的非射血模式量化,并在生理负荷下射血4小时。研究了新鲜对照心脏(n = 5)和用威斯康星大学溶液保存的心脏(n = 6)。
两组的非工作(非射血)左心室功能无差异,但威斯康星大学溶液保存的心脏左心室压力上升峰值速率高于对照组。然而,当心脏承受生理负荷时,两组的左心室功能有显著差异。6个用威斯康星大学溶液保存的心脏中有3个在4小时灌注终点前衰竭,而所有5个对照心脏在整个4小时内均保持稳定的工作功能。用威斯康星大学溶液保存的心脏在射血模式下功能明显受损。平均值如下(p < 0.05):左心室收缩压(毫米汞柱),对照组105±1,威斯康星大学溶液组86±4;左心室压力上升峰值速率(毫米汞柱/毫秒),对照组3.33±0.11,威斯康星大学溶液组2.39±0.24;心输出量(毫升/分钟/克),对照组400±25,威斯康星大学溶液组288±26;每搏功(毫焦耳/克),对照组20.1±1.3,威斯康星大学溶液组11.9±1.1;左心室舒张末期压力(毫米汞柱),对照组5.4±0.3,威斯康星大学溶液组10.2±1.3;主动脉峰值流速(毫升/分钟),对照组946±9,威斯康星大学溶液组659±44;30分钟每焦耳每搏功产生的乳酸毫摩尔数,对照组0.50±0.06,威斯康星大学溶液组6.99±0.37。
这些结果表明,(1)在这种改良的威斯康星大学溶液中低温保存不能充分保存心脏以长时间支持生理负荷,(2)用非射血心脏模型评估保存后的功能不能准确预测保存心脏支持生理负荷的能力。