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再灌注前逆行输注利多卡因或L-精氨酸可减小心肌梗死面积。

Retrograde infusion of lidocaine or L-arginine before reperfusion reduces myocardial infarct size.

作者信息

Lee R, Nitta T, Schmid R A, Schuessler R B, Harris K M, Gay W A

机构信息

Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Ann Thorac Surg. 1998 May;65(5):1353-9. doi: 10.1016/s0003-4975(98)00186-6.

Abstract

BACKGROUND

Retrograde perfusion preserves ischemic myocardium when initiated shortly after coronary artery occlusion. However, benefits diminish as the delay increases. In this study, we used this technique to deliver agents known to reduce the injury associated with the reperfusion of ischemic myocardium. We proposed that the local delivery of lidocaine or L-arginine before reperfusion would reduce the damage caused during reperfusion, even after a delay between onset of ischemia and intervention designed to approximate clinical reality.

METHODS

In a porcine model of myocardial ischemia, the left anterior descending coronary artery was snared immediately distal to its second diagonal branch. After 1 hour of occlusion, 34 animals were randomized into six groups: no intervention (control) (n = 6); administration of normal saline solution into the great cardiac vein (Retro-NS) (n = 6); administration of lidocaine either intravenously (i.v.-LID) (n = 6) or retrograde (Retro-LID) (n = 6); and administration of L-arginine either intravenously (i.v.-L-ARG) (n = 5) or retrograde (Retro-L-ARG) (n = 5). After 90 minutes of ischemia, the snare was released, and the myocardium was reperfused for 3 hours. Two-dimensional echocardiograms were made prior to occlusion and 60, 150, 210, and 270 minutes after occlusion. The infarct size and the area at risk were determined by lissamine green and triphenyltetrazolium chloride staining with computer planimetric quantification. Regional wall motion was assessed by a wall motion score: normal = 1; mild hypokinesia = 2.0; severe hypokinesia = 2.5; and akinesia = 3.

RESULTS

The area of the left ventricle at risk for infarction was similar in all groups and represented 25.4% (5.2% [standard deviation]) of the left ventricular mass (p = 0.63). The percent area of infarction in the area at risk after 3 hours of reperfusion was 76.7% (7.1% for the control group, 73.9% (5.7%) for the Retro-NS group, 72.1% (8.7%) for the i.v.-LID group, 54.5% (10.2%) for the Retro-LID group, 58.8% (4.0%) for the i.v.-L-ARG group, and 54.3% (4.0%) for the Retro-L-ARG group p < 0.005, Retro-LID and Retro-L-ARG versus Control, Retro-NS, and i.v.-LID; p < 0.03, i.v.-L-ARG versus control and Retro-NS). No significant difference in wall motion scores between groups was detected by echocardiography (p = 0.578).

CONCLUSIONS

Retrograde delivery of lidocaine or L-arginine before reperfusion reduces infarct size without acutely affecting wall motion after 90 minutes of ischemia and 3 hours of reperfusion. Lidocaine must be present before reperfusion to have an effect, whereas L-arginine is beneficial if it is delivered at the time of reperfusion.

摘要

背景

冠状动脉闭塞后不久开始逆行灌注可保护缺血心肌。然而,随着延迟时间增加,益处会减少。在本研究中,我们使用该技术来递送已知可减少与缺血心肌再灌注相关损伤的药物。我们提出,在再灌注前局部递送利多卡因或L-精氨酸将减少再灌注期间造成的损伤,即使在缺血发作与旨在模拟临床实际情况的干预之间存在延迟。

方法

在猪心肌缺血模型中,在左前降支冠状动脉第二对角支远端立即用圈套器套扎。闭塞1小时后,34只动物被随机分为六组:不干预(对照组)(n = 6);向心大静脉内注入生理盐水(逆行生理盐水组)(n = 6);静脉注射利多卡因(静脉利多卡因组)(n = 6)或逆行注射利多卡因(逆行利多卡因组)(n = 6);静脉注射L-精氨酸(静脉L-精氨酸组)(n = 5)或逆行注射L-精氨酸(逆行L-精氨酸组)(n = 5)。缺血90分钟后,松开圈套器,心肌再灌注3小时。在闭塞前以及闭塞后60、150、210和270分钟进行二维超声心动图检查。通过丽丝胺绿和氯化三苯基四氮唑染色及计算机平面测量法确定梗死面积和危险区域。通过壁运动评分评估局部壁运动:正常 = 1;轻度运动减弱 = 2.0;重度运动减弱 = 2.5;无运动 = 3。

结果

所有组梗死危险的左心室面积相似,占左心室质量的25.4%(标准差5.2%)(p = 0.63)。再灌注3小时后,危险区域内梗死面积百分比为76.7%(对照组为7.1%,逆行生理盐水组为73.9%(5.7%),静脉利多卡因组为72.1%(8.7%),逆行利多卡因组为54.5%(10.2%),静脉L-精氨酸组为58.8%(4.0%),逆行L-精氨酸组为54.3%(4.0%),p < 0.005,逆行利多卡因组和逆行L-精氨酸组与对照组、逆行生理盐水组和静脉利多卡因组相比;p < 0.03,静脉L-精氨酸组与对照组和逆行生理盐水组相比)。超声心动图未检测到组间壁运动评分有显著差异(p = 0.578)。

结论

再灌注前逆行递送利多卡因或L-精氨酸可减少梗死面积,在缺血90分钟和再灌注3小时后不会急性影响壁运动。利多卡因必须在再灌注前存在才能发挥作用,而L-精氨酸在再灌注时递送则有益。

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