11 C-DPA-713 has much greater specific binding to translocator protein 18?kDa (TSPO) in human brain than 11 C-( R )-PK11195

摘要

Positron emission tomography (PET) radioligands for translocator protein 18?kDa (TSPO) are widely used to measure neuroinflammation, but controversy exists whether second-generation radioligands are superior to the prototypical agent~(11)C-( R )-PK11195 in human imaging. This study sought to quantitatively measure the “signal to background” ratio (assessed as binding potential ( BP _(ND))) of~(11)C-( R )-PK11195 compared to one of the most promising second-generation radioligands,~(11)C-DPA-713. Healthy subjects had dynamic PET scans and arterial blood measurements of radioligand after injection of either~(11)C-( R )-PK11195 (16 subjects) or~(11)C-DPA-713 (22 subjects). To measure the amount of specific binding, a subset of these subjects was scanned after administration of the TSPO blocking drug XBD173 (30–90?mg PO).~(11)C-DPA-713 showed a significant sensitivity to genotype in brain, whereas~(11)C-( R )-PK11195 did not. Lassen occupancy plot analysis revealed that the specific binding of~(11)C-DPA-713 was much greater than that of~(11)C-( R )-PK11195. The BP _(ND)in high-affinity binders was about 10-fold higher for~(11)C-DPA-713 (7.3) than for~(11)C-( R )-PK11195 (0.75). Although the high specific binding of~(11)C-DPA-713 suggests it is an ideal ligand to measure TSPO, we also found that its distribution volume increased over time, consistent with the accumulation of radiometabolites in brain.