Department of Nuclear Medicine, First Hospital of Shanxi Medical University, Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Key Laboratory of Molecular Imaging, Shanxi Medical University, Taiyuan, 030001, China.
Mol Imaging Biol. 2024 Aug;26(4):680-692. doi: 10.1007/s11307-024-01919-9. Epub 2024 Apr 25.
Atherosclerosis remains the pathological basis of myocardial infarction and ischemic stroke. Early and accurate identification of plauqes is crucial to improve clinical outcomes of atherosclerosis patients. Our study aims to evaluate the potential value of fibroblast activation protein inhibitor (FAPI)-04 PET/CT in identifying plaques via a preclinical rabbit model of atherosclerosis.
New Zealand white rabbits were fed high-fat diet (HFD), and randomly divided into the model group injured by the balloon, and the sham group only with incisions. Ultrasound was performed to detect plaques, and FAPI-avid was determined through AlF-NOTA-FAPI-04 PET/CT. Mean standardized uptake values (SUVmean) in lesions were compared, and biodistribution of AlF-NOTA-FAPI-04 and target-to-background ratios (TBRs) were calculated. Histological staining was performed to display arterial plaques, and autoradiography (ARG) was employed to measure the in vitro intensity of AlF-NOTA-FAPI-04. At last, the correlation among FAP levels, plaque area, SUVmean values and fibrous cap thickness was assessed.
The rabbit carotid and abdominal atherosclerosis model was established. AlF-NOTA-FAPI-04 showed a higher uptake in carotid plaques (SUVmean 1.32 ± 0.11) and abdominal plaques (SUVmean 0.73 ± 0.13) compared to corresponding controls (SUVmean 1.07 ± 0.06; 0.46 ± 0.03) (P < 0.05). Biodistribution analysis of AlF-NOTA-FAPI-04 revealed that the bigger plaques were delineated with higher TBRs. Pathological staining showed the formation of arterial plaques, and ARG staining exhibited a higher intensity of AlF-NOTA-FAPI-04 in the bigger plaques. Lastly, plaque area was found to be positively correlated to FAP expression and SUVmean, while FAP expression was negatively correlated to fibrous cap thickness of plaques.
We successfully achieve molecular imaging of fibroblast activation in atherosclerotic lesions of rabbits, suggesting AlF-NOTA-FAPI-04 PET/CT may be a potentially valuable tool to identify plaques.
动脉粥样硬化仍然是心肌梗死和缺血性卒中的病理基础。早期、准确地识别斑块对于改善动脉粥样硬化患者的临床预后至关重要。本研究旨在通过动脉粥样硬化兔模型评估成纤维细胞激活蛋白抑制剂(FAPI)-04 PET/CT 识别斑块的潜在价值。
新西兰白兔给予高脂饮食(HFD),并随机分为球囊损伤模型组和仅切口假手术组。通过超声检测斑块,并通过 AlF-NOTA-FAPI-04 PET/CT 检测 FAPI 活性。比较病灶的平均标准化摄取值(SUVmean),计算 AlF-NOTA-FAPI-04 的生物分布和靶与背景比(TBR)。进行动脉斑块的组织学染色,并进行 Autoradiography(ARG)测量 AlF-NOTA-FAPI-04 的体外强度。最后,评估 FAP 水平、斑块面积、SUVmean 值与纤维帽厚度之间的相关性。
成功建立了兔颈动脉和腹主动脉粥样硬化模型。AlF-NOTA-FAPI-04 在颈动脉斑块(SUVmean 1.32±0.11)和腹主动脉斑块(SUVmean 0.73±0.13)中的摄取明显高于相应对照组(SUVmean 1.07±0.06;0.46±0.03)(P<0.05)。AlF-NOTA-FAPI-04 的生物分布分析显示,较大的斑块具有更高的 TBR。病理学染色显示动脉斑块形成,ARG 染色显示较大斑块中 AlF-NOTA-FAPI-04 的强度更高。最后,斑块面积与 FAP 表达和 SUVmean 呈正相关,而 FAP 表达与斑块纤维帽厚度呈负相关。
本研究成功实现了兔动脉粥样硬化病变中成纤维细胞激活的分子成像,提示 AlF-NOTA-FAPI-04 PET/CT 可能是一种有价值的识别斑块的工具。