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递增剂量的多巴酚丁胺在冠状动脉狭窄所累及的功能失调左心室区域诱发双相反应。

Incremental doses of dobutamine induce a biphasic response in dysfunctional left ventricular regions subtending coronary stenoses.

作者信息

Chen C, Li L, Chen L L, Prada J V, Chen M H, Fallon J T, Weyman A E, Waters D, Gillam L

机构信息

Division of Cardiology, Hartford Hospital, University of Connecticut 06102, USA.

出版信息

Circulation. 1995 Aug 15;92(4):756-66. doi: 10.1161/01.cir.92.4.756.

DOI:10.1161/01.cir.92.4.756
PMID:7641353
Abstract

BACKGROUND

Dobutamine stress echocardiography has been proposed as a diagnostic tool to identify viable myocardium. How regional wall thickening responds to dobutamine in the ischemic or short-term hibernating myocardium has not been adequately defined. We hypothesized that regional wall thickening would improve initially and subsequently deteriorate with incremental doses of dobutamine in viable myocardial regions supplied by a stenotic coronary artery. This study was undertaken to determine whether this biphasic pattern of regional function characterizes the response of ischemic or hibernating myocardium to dobutamine and to explore the factors and mechanisms that determine this response.

METHODS AND RESULTS

Twenty-six pigs in four groups were studied: a control group (n = 5) to assess the response of myocardium perfused by nonstenotic coronary artery to incremental doses of dobutamine, and three experimental groups with a left anterior descending coronary artery stenosis producing acute myocardial ischemia (n = 7), short-term myocardial hibernation for 90 minutes (n = 7), and short-term hibernation for 24 hours (n = 7) to determine the functional and metabolic response to dobutamine under these conditions. Regional coronary flow was reduced to 40% to 60% of baseline, with significant reductions of regional wall thickening as measured by two-dimensional echocardiography and sonomicrometers. An incremental dobutamine infusion from 2.5 to 25 micrograms.kg-1.min-1 increased wall thickening and coronary flow without lactate production in the control group. In the other three groups, during the incremental dobutamine infusion, regional wall thickening improved initially, from 11.4 +/- 7.5% to 19.8 +/- 11.4%, P < .01, at dobutamine doses of 2.5 to 10 (4.5 +/- 2.2) micrograms.min-1.kg-1 but deteriorated subsequently to 5.0 +/- 5.8% at the maximal dose of dobutamine of 12.6 +/- 4.1 micrograms.min-1.kg-1. The initial improvement of regional wall thickening was associated with a small increase in regional coronary flow (from 0.53 +/- 0.18 to 0.68 +/- 0.25 mL.min-1.g-1 myocardium, P < .05) and with regional lactate production. High doses of dobutamine did not further increase regional coronary flow but markedly increased lactate production and induced regional myocardial acidosis (pH 7.26 +/- 0.07). The biphasic pattern of response to dobutamine was observed in each of the three experimental groups. Both peak improvement and peak deterioration occurred earlier and at lower dobutamine dose levels in the group with acute ischemia compared with the group with short-term hibernation for 24 hours (P < .05).

CONCLUSIONS

A biphasic response of wall thickening to incremental dobutamine with initial improvement and subsequent deterioration is characteristic of ischemic or short-term hibernating myocardium. The initial low-dose dobutamine infusion improved wall thickening in the ischemic or hibernating myocardial region to a modest level. This initial modest improvement was transient and at the expense of metabolic deterioration of myocardial ischemia, so that at higher doses during prolonged dobutamine infusion, wall thickening deteriorated, lactate accumulated, and myocardial acidosis developed.

摘要

背景

多巴酚丁胺负荷超声心动图已被提议作为一种识别存活心肌的诊断工具。在缺血或短期冬眠心肌中,室壁增厚对多巴酚丁胺的反应尚未得到充分明确。我们假设在由狭窄冠状动脉供血的存活心肌区域,室壁增厚最初会改善,随后随着多巴酚丁胺剂量增加而恶化。本研究旨在确定这种室壁功能的双相模式是否为缺血或冬眠心肌对多巴酚丁胺反应的特征,并探索决定这种反应的因素和机制。

方法与结果

对四组共26头猪进行了研究:一个对照组(n = 5),以评估由非狭窄冠状动脉供血的心肌对多巴酚丁胺递增剂量的反应;三个实验组,通过左前降支冠状动脉狭窄造成急性心肌缺血(n = 7)、短期心肌冬眠90分钟(n = 7)和短期冬眠24小时(n = 7),以确定在这些情况下对多巴酚丁胺的功能和代谢反应。局部冠状动脉血流减少至基线的40%至60%二维超声心动图和体腔微测仪测量显示室壁增厚显著降低。对照组中,多巴酚丁胺以2.5至25微克·千克⁻¹·分钟⁻¹递增输注,增加了室壁增厚和冠状动脉血流,且无乳酸生成。在其他三组中,多巴酚丁胺递增输注期间,室壁增厚最初改善,在多巴酚丁胺剂量为2.5至10(4.5±2.2)微克·分钟⁻¹·千克⁻¹时,从11.4±7.5%改善至19.8±11.4%,P < 0.01,但随后在多巴酚丁胺最大剂量12.6±4.1微克·分钟⁻¹·千克⁻¹时恶化至5.0±5.8%。室壁增厚的初始改善与局部冠状动脉血流的小幅增加(从0.53±0.18至0.68±0.25毫升·分钟⁻¹·克⁻¹心肌,P < 0.05)以及局部乳酸生成有关。高剂量多巴酚丁胺未进一步增加局部冠状动脉血流,但显著增加了乳酸生成并导致局部心肌酸中毒(pH 7.26±0.07)。在三个实验组中均观察到了对多巴酚丁胺的双相反应模式。与短期冬眠24小时的组相比,急性缺血组的峰值改善和峰值恶化均更早出现且多巴酚丁胺剂量水平更低(P < 0.05)。

结论

室壁增厚对递增多巴酚丁胺呈现双相反应,最初改善随后恶化,这是缺血或短期冬眠心肌的特征。初始低剂量多巴酚丁胺输注使缺血或冬眠心肌区域的室壁增厚改善至适度水平。这种初始适度改善是短暂的,且以心肌缺血代谢恶化为代价,因此在多巴酚丁胺长时间输注的较高剂量时,室壁增厚恶化,乳酸蓄积,心肌酸中毒发生。

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