Sun Zhongchan, Tong Guang, Liu Yuanhui, Fan Hualin, He Weibin, Wang Bo, Xia Shuang, He Pengcheng
Guangdong Provincial Key Laboratory of Coronary Heart Disease Prevention, Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Department of Cardiology, Ganzhou Municipal Hospital, Ganzhou, China.
Front Cardiovasc Med. 2022 Feb 8;9:738076. doi: 10.3389/fcvm.2022.738076. eCollection 2022.
Peripheral arterial disease (PAD) leads to tissue ischemia in the extremities. Enhanced vascular permeability plays a critical role in targeted delivery of drugs for effective therapeutic angiogenesis and resultant blood perfusion recovery. However, optimal tracers for evaluating this process in PAD patients are lacking. At this time, we employed a novel albumin-labeling tracer of dual function, termed as F-NEB, to assess blood perfusion as well as vascular permeability by positron emission tomography (PET).
After successful establishment of mouse hindlimb ischemia (HI) model, static PET imaging was performed 15 min and 2 h post injection (p.i.) of F-NEB at 1, 3, 5, 7, 10 and 14 days post-surgery respectively. Gradual recovery of blood supply was detected by PET scan 15 min p.i. and collaborated by serial Laser Doppler. In addition, the highest vascular permeability observed by high local uptake of F-NEB at 2 h p.i. was consistent with histological examinations. Furthermore, we quantitatively evaluated the effect of vascular endothelial growth factor (VEGF) stimulus on vascular permeability and blood perfusion by PET scan using F-NEB probe in HI model, which were also confirmed by immunohistological results.
The application of F-NEB probe alone by PET can successfully achieve dual imaging of blood perfusion as well as vascular permeability at different time points p.i. and monitor their responses to therapy in PAD model. The simple labeling approach and multipurpose feature suggest the great promise of using this imaging probe in theranostic applications for treating ischemic disease.
外周动脉疾病(PAD)导致肢体组织缺血。增强的血管通透性在药物靶向递送以实现有效的治疗性血管生成和随后的血流灌注恢复中起着关键作用。然而,缺乏用于评估PAD患者这一过程的最佳示踪剂。此时,我们采用了一种新型的具有双重功能的白蛋白标记示踪剂,称为F-NEB,通过正电子发射断层扫描(PET)来评估血流灌注以及血管通透性。
成功建立小鼠后肢缺血(HI)模型后,分别在术后1、3、5、7、10和14天注射F-NEB后15分钟和2小时进行静态PET成像。注射后15分钟通过PET扫描检测到供血逐渐恢复,并经系列激光多普勒验证。此外,注射后2小时F-NEB局部高摄取所观察到的最高血管通透性与组织学检查结果一致。此外,我们在HI模型中使用F-NEB探针通过PET扫描定量评估了血管内皮生长因子(VEGF)刺激对血管通透性和血流灌注的影响,免疫组织学结果也证实了这一点。
单独使用F-NEB探针通过PET能够在注射后不同时间点成功实现血流灌注和血管通透性的双重成像,并监测它们在PAD模型中对治疗的反应。这种简单的标记方法和多功能特性表明,在治疗缺血性疾病的诊疗应用中使用这种成像探针具有巨大的前景。