Quantification of 5-HT1A receptors in human brain using p-MPPF kinetic modelling and PET
(2002) European journal of nuclear medicine — Vol. 29, n° 1, p. 76-81 (2002)
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- Abstract
- Serotonin-1A (5-HT1A) receptors are implicated in neurochemical mechanisms underlying anxiety and depression and their treatment. Animal studies have suggested that 4-(2'-methoxyphenyl)-1-[2'-[N-(2"-pyridinyl)-p-[F-18]fluorobenzamido] ethyl] piperazine (p-MPPF) may be a suitable positron emission tomography (PET) tracer of 5-HT1A receptors. To test p-MPPF in humans, we performed 60-min dynamic PET scans in 13 healthy volunteers after single bolus injection. Metabolite quantification revealed a fast decrease in tracer plasma concentration, such that at 5 min post injection about 25% of the total radioactivity in plasma corresponded to p-MPPF. Radioactivity concentration was highest in hippocampus, intermediate in neocortex and lowest in basal ganglia and cerebellum. The interactions between p-MPPF and 5-HT1A receptors were described using linear compartmental models with plasma input and reference tissue approaches. The two quantification methods provided similar results which are in agreement with previous reports on 5-HT1A receptor brain distribution. In conclusion, our results show that p-MPPF is a suitable PET radioligand for 5-HT1A receptor human studies.
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Sanabria-Bohorquez, S. M., Biver, F., Damhaut, P., Wikler, D., Veraart, C., & Goldman, S. (2002). Quantification of 5-HT1A receptors in human brain using p-MPPF kinetic modelling and PET. European journal of nuclear medicine, 29(1), 76-81. https://doi.org/10.1007/s00259-001-0684-2 (Original work published 2002)