Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
J Nucl Med. 2013 Aug;54(8):1397-403. doi: 10.2967/jnumed.112.112490. Epub 2013 Jun 26.
High-dose ionizing irradiation can cause extensive injuries in susceptible tissues. A noninvasive imaging technique that detects a surrogate marker of apoptosis may help characterize the dynamics of radiation-induced tissue damage. The goal of this study was to prove the concept of imaging the temporal and spatial distribution of damage in susceptible tissues after high-dose radiation exposure, using (99m)Tc-duramycin as a phosphatidylethanolamine-binding radiopharmaceutical.
Rats were subjected to 15 Gy of total-body irradiation with x-rays. Planar whole-body (99m)Tc-duramycin scanning (n = 4 per time point) was conducted at 24, 48, and 72 h using a clinical γ-camera. On the basis of findings from planar imaging, preclinical SPECT data were acquired on control rats and on irradiated rats at 6 and 24 h after irradiation (n = 4 per time point). Imaging data were validated by γ-counting and histology, using harvested tissues in parallel groups of animals (n = 4).
Prominent focal uptake was detected in the thymus as early as 6 h after irradiation, followed by a gradual decline in (99m)Tc-duramycin binding accompanied by extensive thymic atrophy. Early (6-24 h) radioactivity uptake in the gastrointestinal region was detected. Significant signal was seen in major bones in a slightly delayed fashion, at 24 h, which persisted for at least 2 d. This finding was paralleled by an elevation in signal intensity in the kidneys, spleen, and liver. The imaging results were consistent with ex vivo γ-counting results and histology. Relatively high levels of apoptosis were detected from histology in the thymus, guts, and bones, with the thymus undergoing substantial atrophy.
As a proof of principle, this study demonstrated a noninvasive imaging technique that allows characterization of the temporal and spatial dynamics of injuries in susceptible tissues during the acute phase after high-dose ionizing irradiation. Such an imaging capability will potentially be useful for global, whole-body, assessment of tissue damage after radiation exposure. These data, in turn, will contribute to our general knowledge of tissue susceptibility to ionizing irradiation, as well as the onset and progression of tissue injuries.
高剂量电离辐射会导致敏感组织广泛损伤。一种非侵入性的成像技术,检测细胞凋亡的替代标志物,可能有助于描述辐射诱导组织损伤的动力学。本研究的目的是证明使用(99m)Tc- duramycin 作为一种磷脂酰乙醇胺结合放射性药物,对高剂量辐射暴露后敏感组织中损伤的时间和空间分布进行成像的概念。
用 X 射线对大鼠进行 15Gy 全身照射。用临床γ-相机在 24、48 和 72 小时进行(99m)Tc- duramycin 全身平面扫描(每个时间点 4 只)。基于平面成像的结果,在对照大鼠和照射后 6 和 24 小时的照射大鼠上进行临床前 SPECT 数据采集(每个时间点 4 只)。通过γ计数和组织学对成像数据进行验证,同时在平行的动物组中采集组织(每组 4 只)。
照射后 6 小时,胸腺内即可检测到明显的局灶性摄取,随后(99m)Tc- duramycin 结合逐渐减少,伴广泛的胸腺萎缩。早期(6-24 小时)胃肠道区域有放射性摄取。24 小时时,骨骼中可见稍延迟的明显信号,至少持续 2 天。这一发现与肾脏、脾脏和肝脏信号强度的升高相一致。成像结果与离体γ计数结果和组织学一致。从组织学上看,胸腺、肠道和骨骼中检测到相对较高水平的凋亡,胸腺发生了实质性萎缩。
作为原理验证,本研究证明了一种非侵入性的成像技术,允许在高剂量电离辐射后急性相期间描述敏感组织损伤的时间和空间动态。这种成像能力可能对全身照射后组织损伤的全面、全身评估有用。这些数据反过来将有助于我们对组织对电离辐射的敏感性、组织损伤的发生和进展的一般认识。