Okada David R, Johnson Gerald, Liu Zhonglin, Hocherman Sonia D, Khaw Ban-An, Okada Robert D
Department of Biology, University of Tulsa, Tulsa, Oklahoma, USA.
J Nucl Med. 2004 Apr;45(4):655-64.
99mTc-Glucarate is an infarct-avid imaging agent with the potential for very early detection of myocardial infarction. The purposes of this study using a canine model were to determine (a) the time course of (99m)Tc-glucarate uptake and clearance from necrotic and normal myocardium; (b) the (99m)Tc-glucarate necrotic-to-normal activity ratio over time; (c) the time course of detectable scan positivity after intravenous administration of the tracer; and (d) the relationship of infarct size determined by triphenyltetrazolium chloride (TTC) staining versus (99m)Tc-glucarate imaging ex vivo.
A 90-min left circumflex coronary artery (LCx) occlusion was followed by 270 min of reperfusion at 100% baseline flow in 6 open-chest, anesthetized dogs. (99m)Tc-Glucarate (555 MBq [15 mCi]) was injected 30 min after reperfusion and was followed by 240 min of gamma-camera serial imaging. Microspheres were injected during baseline, occlusion, tracer injection, and before the dogs were euthanized. Creatine kinase assays were performed to assess developing injury. Ex vivo gamma-camera imaging was performed. Blood flow and tracer activity were determined by well counting. TTC stain was used to mark infarct areas, which were sized using computerized digital planimetry.
Hemodynamics demonstrated no significant change from baseline at any time for any parameter except LCx flow, which was significantly depressed during occlusion. The mean infarct size +/- SEM was 10.7% +/- 2% of total left ventricle. Blood (99m)Tc-glucarate clearance was triexponential and rapid. Qualitative image analysis revealed a well defined hot spot after 30 min, which remained well defined through 240 min after injection (150 and 360 min after occlusion, respectively). Images were quantitatively abnormal with hot spot-to-normal zone activity ratios of >/=2:1 within 10 min of tracer administration (130 min after occlusion), reaching 8:1 at 240 min after tracer administration (360 min after occlusion). There was a linear correlation between infarct size determined by (99m)Tc-glucarate and TTC staining (r = 0.96; slope = 0.87).
(99m)Tc-Glucarate marks acute myocardial infarct very early after occlusion and appears to accurately assess infarct size when compared with TTC staining.
99mTc-葡糖醛酸是一种梗死灶摄取显像剂,具有极早期检测心肌梗死的潜力。本研究采用犬模型的目的是确定:(a) 99mTc-葡糖醛酸在坏死心肌和正常心肌中的摄取和清除时间过程;(b) 99mTc-葡糖醛酸坏死与正常心肌活性比值随时间的变化;(c) 静脉注射示踪剂后可检测到的扫描阳性的时间过程;(d) 通过氯化三苯基四氮唑 (TTC) 染色确定的梗死面积与离体99mTc-葡糖醛酸显像之间的关系。
对6只开胸麻醉犬进行90分钟的左旋冠状动脉 (LCx) 闭塞,然后在100% 基线血流下再灌注270分钟。再灌注30分钟后注射99mTc-葡糖醛酸 (555 MBq [15 mCi]),随后进行240分钟的γ相机连续显像。在基线、闭塞、示踪剂注射期间以及犬安乐死之前注射微球。进行肌酸激酶测定以评估损伤发展情况。进行离体γ相机显像。通过井型计数法测定血流和示踪剂活性。使用TTC染色标记梗死区域,并用计算机数字平面测量法测量其大小。
除LCx血流在闭塞期间显著降低外,任何参数在任何时间的血流动力学与基线相比均无显著变化。平均梗死面积±标准误为左心室总面积的10.7%±2%。血液中99mTc-葡糖醛酸的清除呈三指数且快速。定性图像分析显示,30分钟后出现明确的热点,注射后240分钟(分别为闭塞后150和360分钟)仍保持明确。图像在定量上异常,示踪剂给药后10分钟内(闭塞后130分钟)热点与正常区域活性比值≥2:1,示踪剂给药后240分钟(闭塞后360分钟)达到8:1。99mTc-葡糖醛酸测定的梗死面积与TTC染色之间存在线性相关性 (r = 0.96;斜率 = 0.87)。
99mTc-葡糖醛酸在闭塞后极早期标记急性心肌梗死,与TTC染色相比,似乎能准确评估梗死面积。