Rumsey W L, Kuczynski B, Patel B, Bauer A, Narra R K, Eaton S M, Nunn A D, Strauss H W
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey.
J Nucl Med. 1995 Aug;36(8):1445-50.
This investigation evaluates the efficacy of a 99mTc-labeled nitroimidazole (BMS-181321) in identifying oxygen-deprived tissue in two canine models of myocardial ischemia.
For both models (A and B), epicardial microvascular oxygen pressure (mPO2) was monitored by measuring the oxygen-dependent quenching of phosphorescence lifetime of Palladium mesotetra (4-carboxyphenyl) porphine. In Model A (beagles, n = 5), BMS-181321 was administered intravenously and a distal branch of the left anterior descending coronary artery (LAD) was ligated completely 40 sec later. Ten minutes later, the ligature was released establishing tissue reoxygenation. In Model B, flow through the LAD was reduced until the mPO2 was about 2 Torr. After bolus administration of BMS-181321 (50-60 mCi), coronary ischemia was continued for a residence period of up to 4 hr.
With Model A, SPECT reconstructions revealed a small ischemic area in three of five dogs, however, a transmural accumulation of the compound was evident in the autoradiograms from all dogs. In the two animals in which the defect was not observed by SPECT, the ischemic episode had nominal effects on the ratio of +/- dp/dt (< 4% change as compared to baseline values). In Model B, SPECT reconstructions showed positive images of the oxygen-deprived area within the mid- to apical regions of the left ventricle (n = 5). Autoradiographic analysis showed a transmural association with cells resulting in an ischemic-to-nonischemic ratio of 3.5 +/- 0.4 (n = 4) for animals with similar residence times.
The results from both models suggest that BMS-181321 provides a noninvasive marker of regional ischemia in the heart and that this compound may have clinical utility for detection of coronary artery disease.
本研究评估了99mTc标记的硝唑咪(BMS - 181321)在两种犬心肌缺血模型中识别缺氧组织的效能。
对于两种模型(A和B),通过测量钯中四(4 - 羧基苯基)卟啉磷光寿命的氧依赖性猝灭来监测心外膜微血管氧分压(mPO2)。在模型A(比格犬,n = 5)中,静脉注射BMS - 181321,40秒后完全结扎左前降支冠状动脉(LAD)的一个远端分支。10分钟后,松开结扎线使组织再氧合。在模型B中,减少通过LAD的血流直至mPO2约为2托。静脉推注BMS - 181321(50 - 60毫居里)后,冠状动脉缺血持续长达4小时。
在模型A中,SPECT重建显示五只犬中有三只存在小的缺血区域,然而,在所有犬的放射自显影片中均可见该化合物的透壁积聚。在SPECT未观察到缺损的两只动物中,缺血发作对±dp/dt比值的影响很小(与基线值相比变化<4%)。在模型B中,SPECT重建显示左心室中至心尖区域内缺氧区域的阳性图像(n = 5)。放射自显影分析显示该化合物与细胞存在透壁相关性,对于停留时间相似的动物,缺血与非缺血比值为3.5±0.4(n = 4)。
两种模型的结果均表明,BMS - 181321可提供心脏局部缺血的非侵入性标志物,且该化合物可能对冠状动脉疾病的检测具有临床应用价值。