Glover D K, Ruiz M, Sansoy V, Barrett R J, Beller G A
Department of Medicine, University of Virginia Health Sciences Center, Charlottesville 22908.
J Nucl Med. 1995 Feb;36(2):270-5.
N6-endonorboman-2-yl-9-methyladenine (N-0861) is a drug which inhibits the A1 adenosine receptor subtype. One proposed use for N-0861 is to eliminate A1 receptor-mediated side effects such as A-V heart block and possibly angina in patients undergoing pharmacologic stress with adenosine. The goal of this study was to determine whether N-0861 has any crossover effect on the A2 vasodilatory action of adenosine or on 201TI uptake which would adversely affect imaging of coronary stenoses.
In eight dogs with critical left anterior descending (LAD) stenoses, we compared the hemodynamic response to intravenous adenosine (250 micrograms/kg/min) before and after N-0861 administration. LAD and left circumflex (LCx) coronary flows were measured ultrasonically and regional blood flow was assessed using microspheres. Thallium-201 (18.5-37.0 MBq) was injected during adenosine hyperemia while N-0861 was present. Imaging of heart slices was performed and defect magnitude was calculated as LAD:LCx count ratios from regions of interest (ROIs) on images. Regional 201Tl activity and microsphere flow were determined by gamma well counting.
There was no change in mean heart rate, arterial and left atrial pressures, +dP/dt, and ultrasonically measured LAD and LCx coronary flows upon N-0861 administration. In addition, adenosine evoked a similar hemodynamic response after N-0861. There was also no change in coronary flow in the critically stenotic LAD but LCx flow tripled to 106 +/- 14 ml/min (p < 0.01).
These data indicate that N-0861 pretreatment does not adversely affect adenosine A2 receptor-mediated vasodilation and has no effect on the detection of a critical coronary stenosis by 201Tl imaging. Thus, the pretreatment strategy may prove useful for the elimination of A1 receptor-mediated side effects during pharmacologic stress imaging with adenosine.
N6-内降冰片-2-基-9-甲基腺嘌呤(N-0861)是一种抑制A1腺苷受体亚型的药物。N-0861的一种潜在用途是消除腺苷药物负荷试验患者中A1受体介导的副作用,如房室传导阻滞以及可能的心绞痛。本研究的目的是确定N-0861是否对腺苷的A2血管舒张作用或对201铊摄取有任何交叉效应,而这可能会对冠状动脉狭窄的成像产生不利影响。
在8只患有严重左前降支(LAD)狭窄的犬中,我们比较了静脉注射腺苷(250微克/千克/分钟)在给予N-0861之前和之后的血流动力学反应。使用超声测量LAD和左旋支(LCx)冠状动脉血流,并使用微球评估局部血流。在存在N-0861的情况下,在腺苷充血期间注射201铊(18.5 - 37.0兆贝可)。对心脏切片进行成像,并将缺损大小计算为图像上感兴趣区域(ROI)的LAD:LCx计数比。通过伽马计数管确定局部201铊活性和微球流量。
给予N-0861后,平均心率、动脉压和左心房压、+dP/dt以及超声测量的LAD和LCx冠状动脉血流均无变化。此外,在给予N-0861后,腺苷引起了类似的血流动力学反应。严重狭窄的LAD冠状动脉血流也没有变化,但LCx血流增加了两倍,达到106±14毫升/分钟(p < 0.01)。
这些数据表明,N-0861预处理不会对腺苷A2受体介导的血管舒张产生不利影响,并且对通过201铊成像检测严重冠状动脉狭窄没有影响。因此,这种预处理策略可能被证明对于消除腺苷药物负荷试验成像期间A1受体介导的副作用是有用的。