Croteau Etienne, Bénard François, Bentourkia M'hamed, Rousseau Jacques, Paquette Michel, Lecomte Roger
Département de médecine nucléaire et radiobiologie, Université de Sherbrooke, Sherbrooke, Québec J1H 5N4, Canada.
J Nucl Med. 2004 Nov;45(11):1924-30.
The purpose of this study was to evaluate the effects of 2 anesthetic agents on myocardial perfusion and coronary reserve in rats under resting and stress conditions with small animal PET.
Twenty-four rest/stress studies were performed in 6 rats. Each animal received all 4 possible combinations of anesthetic agents (propofol, isoflurane) and pharmacologic stress agents (dobutamine, adenosine) to increase myocardial perfusion. For each stress or rest study, a 10-min dynamic acquisition was performed in list mode with 185 MBq of (13)N-NH(3). Data analysis was performed according to a 3-compartment myocardial blood flow model. Pharmacologic stimulation by either dobutamine or adenosine was performed to increase myocardial perfusion.
The perfusion values (mean +/- SD) for the various experimental conditions were as follows: propofol/dobutamine, 7.8 +/- 2.4 mL/g/min (rest, 3.7 +/- 0.8 mL/g/min; mean +/- SD); isoflurane/dobutamine, 9.3 +/- 3.1 mL/g/min (rest, 4.3 +/- 1.0 mL/g/min); propofol/adenosine, 6.8 +/- 1.7 mL/g/min (rest, 3.2 +/- 0.4 mL/g/min); and isoflurane/adenosine, 5.2 +/- 1.3 mL/g/min (rest, 3.7 +/- 0.7 mL/g/min). All perfusion data showed a significant increase after pharmacologic stimulation relative to baseline (P < 0.05). The coronary reserve (mean +/- SD) measured by PET was slightly lower with the combination of isoflurane and adenosine (1.4 +/- 0.5) than with propofol and adenosine (2.1 +/- 0.5).
Noninvasive quantitative measurements of myocardial perfusion in small animals at rest and during stress are feasible using PET. Evaluation of the coronary reserve must take into account the initial state of the anesthetized animal. The coronary reserve could be measured with both anesthetic agents using either dobutamine or adenosine stimulation.
本研究的目的是使用小动物正电子发射断层扫描(PET)评估两种麻醉剂在静息和应激条件下对大鼠心肌灌注和冠状动脉储备的影响。
对6只大鼠进行了24次静息/应激研究。每只动物接受麻醉剂(丙泊酚、异氟烷)和药理应激剂(多巴酚丁胺、腺苷)的所有4种可能组合,以增加心肌灌注。对于每次应激或静息研究,使用185 MBq的(13)N-NH(3)以列表模式进行10分钟的动态采集。根据三室心肌血流模型进行数据分析。通过多巴酚丁胺或腺苷进行药理刺激以增加心肌灌注。
各种实验条件下的灌注值(平均值±标准差)如下:丙泊酚/多巴酚丁胺,7.8±2.4 mL/g/min(静息,3.7±0.8 mL/g/min;平均值±标准差);异氟烷/多巴酚丁胺,9.3±3. mL/g/min(静息,4.3±1.0 mL/g/min);丙泊酚/腺苷,6.8±1.7 mL/g/min(静息,3.2±0.4 mL/g/min);异氟烷/腺苷,5.2±1.3 mL/g/min(静息,3.7±0.7 mL/g/min)。所有灌注数据在药理刺激后相对于基线均显示出显著增加(P<0.05)。PET测量的冠状动脉储备(平均值±标准差)在异氟烷和腺苷组合(1.4±0.5)时略低于丙泊酚和腺苷组合(2.1±0.5)。
使用PET对小动物静息和应激时的心肌灌注进行无创定量测量是可行的。评估冠状动脉储备必须考虑麻醉动物的初始状态。使用多巴酚丁胺或腺苷刺激时,两种麻醉剂均可测量冠状动脉储备。