Liu Zhonglin, Barrett Harrison H, Stevenson Gail D, Furenlid Lars R, Pak Koon Yan, Woolfenden James M
Department of Radiology, University of Arizona, Tucson, Arizona 85724-5067, USA.
Nucl Med Commun. 2008 Feb;29(2):120-8. doi: 10.1097/MNM.0b013e3282f29702.
To examine the protective role of ischaemic preconditioning (IPC) in rat hearts using Tc-glucarate (GLA) and a stationary SPECT imager, FastSPECT.
Twenty-four rats with 30 min myocardial ischaemia and 150 min reperfusion (IR) were studied as follows. The IPC group (n=6) underwent IPC (five cycles of 4 min ligation of the left coronary artery and reflow) before IR. The control group (n=7) was treated by IR without IPC. The SPT group (n=6) was subjected to IPC and an adenosine antagonist, 8-(p-sulfophenyl)-theophylline (SPT). The vehicle group (n=5) received IPC and SPT carrier vehicle. GLA was delivered intravenously 30 min post-reperfusion, and 2-h dynamic cardiac images were acquired by FastSPECT.
GLA showed 'hot-spot' accumulation in the ischaemic area-at-risk (IAR) and exhibited lower retention (% 5 min peak) in the IPC and vehicle groups (33.8+/-2.6 vs. 35.7+/-9.2, P>0.05) than in the control and SPT groups (63.1+/-5.3 vs. 54.8+/-4.8, P>0.05). The infarct size (% IAR) was larger in the control and SPT groups (48.2+/-6.3 vs. 41.7+/-6.3, P>0.05) than that in the IPC and vehicle groups (21.0+/-1.9 vs. 19.1+/-4.6, P>0.05). In terms of the ex-vivo IAR-to-normal radioactivity ratio, there was a statistical difference between the control and IPC groups (7.4+/-0.9 vs. 3.0+/-0.4), as well as the SPT and vehicle groups (7.4+/-1.0 vs. 3.4+/-0.5).
IPC offers cardioprotection and relates to the activation of adenosine receptors in rat hearts. FastSPECT GLA imaging is not only useful in detecting early ischaemia-reperfusion injury, but also valuable in evaluating cardioprotection.
使用锝 - 葡萄糖醛酸(GLA)和静态单光子发射计算机断层显像仪(SPECT)FastSPECT,研究缺血预处理(IPC)在大鼠心脏中的保护作用。
对24只经历30分钟心肌缺血和150分钟再灌注(IR)的大鼠进行如下研究。IPC组(n = 6)在IR前进行IPC(左冠状动脉结扎4分钟和再灌注的五个循环)。对照组(n = 7)接受无IPC的IR治疗。SPT组(n = 6)进行IPC并给予腺苷拮抗剂8 - (对 - 磺基苯基) - 茶碱(SPT)。载体组(n = 5)接受IPC和SPT载体。再灌注后30分钟静脉注射GLA,并通过FastSPECT采集2小时动态心脏图像。
GLA在缺血危险区(IAR)显示“热点”聚集,并且在IPC组和载体组中的滞留率较低(5分钟峰值时的百分比,分别为33.8±2.6与35.7±9.2,P>0.05),低于对照组和SPT组(分别为63.1±5.3与54.8±4.8,P>0.05)。对照组和SPT组的梗死面积(占IAR的百分比)(分别为48.2±6.3与41.7±6.3,P>0.05)大于IPC组和载体组(分别为21.0±1.9与19.1±4.6,P>0.05)。就体外IAR与正常放射性比值而言,对照组和IPC组之间存在统计学差异(分别为7.4±0.9与3.0±0.4),SPT组和载体组之间也存在统计学差异(分别为7.4±1.0与3.4±0.5)。
IPC提供心脏保护作用,并与大鼠心脏中腺苷受体的激活有关。FastSPECT GLA成像不仅有助于检测早期缺血再灌注损伤,而且在评估心脏保护方面也具有重要价值。