AI Article Synopsis

  • Inflammation from activated macrophages in vulnerable atherosclerotic plaques (VAPs) increases the risk of plaque rupture, and the translocator protein (TSPO) is crucial for detecting this inflammation.
  • The study used F-FDPA radiotracers to image and quantify plaque inflammation in three groups of rabbits, finding significant differences in tracer uptake between those with VAPs and other groups.
  • Results indicated that F-FDPA uptake correlated with increased macrophage presence and inflammation in atherosclerotic plaques, highlighting its potential as an effective method for assessing vascular inflammation.

Article Abstract

Inflammation induced by activated macrophages within vulnerable atherosclerotic plaques (VAPs) constitutes a significant risk factor for plaque rupture. Translocator protein (TSPO) is highly expressed in activated macrophages. This study investigated the effectiveness of TSPO radiotracers, F-FDPA, in detecting VAPs and quantifying plaque inflammation in rabbits. 18 New Zealand rabbits were divided into 3 groups: sham group A, VAP model group B, and evolocumab treatment group C. F-FDPA PET/CTA imaging was performed at 12, 16, and 24 weeks in all groups. Optical coherence tomography (OCT) was performed on the abdominal aorta at 24 weeks. The VAP was defined through OCT images, and aorta PET imaging was also performed at 24 weeks. The SUV and SUV of F-FDPA were measured on the target organ, and the target-to-background ratio (TBR) was calculated as SUV/SUV. The arterial sections of the isolated abdominal aorta were analyzed by HE staining, CD68 and TSPO immunofluorescence staining, and TSPO Western blot. The results showed that at 24 weeks, the plaque TBR of F-FDPA in group B was significantly higher than in groups A and C. Immunofluorescence staining of CD68 and TSPO, as well as Western blot, confirmed the increased expression of macrophages and TSPO in the corresponding regions of group B. HE staining revealed an increased presence of the lipid core, multiple foam cells, and inflammatory cell infiltration in the area with high F-FDPA uptake. This indicates a correlation between F-FDPA uptake, inflammation severity, and VAPs. The TSPO-targeted tracer F-FDPA shows specific uptake in macrophage-rich regions of atherosclerotic plaques, making it a valuable tool for assessing inflammation in VAPs.

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Source
http://dx.doi.org/10.1021/acs.molpharmaceut.4c00344DOI Listing

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