Serotonin 2A receptor agonist binding in the human brain with [C]Cimbi-36

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A. Ettrup, S. da Cunha-Bang, Barry P. McMahon, S. Lehel, A. Dyssegaard, A.W. Skibsted, Louise Møller Jørgensen, M. Hansen, A.O. Baandrup, S. Bache, C. Svarer, Jesper Langgaard Kristensen, N. Gillings, Jacob Madsen, G.M. Knudsen

[C]Cimbi-36 was recently developed as a selective serotonin 2A (5-HT) receptor agonist radioligand for positron emission tomography (PET) brain imaging. Such an agonist PET radioligand may provide a novel, and more functional, measure of the serotonergic system and agonist binding is more likely than antagonist binding to reflect 5-HT levels in vivo. Here, we show data from a first-in-human clinical trial with [C]Cimbi-36. In 29 healthy volunteers, we found high brain uptake and distribution according to 5-HT receptors with [C]Cimbi-36 PET. The two-tissue compartment model using arterial input measurements provided the most optimal quantification of cerebral [C]Cimbi-36 binding. Reference tissue modeling was feasible as it induced a negative but predictable bias in [C]Cimbi-36 PET outcome measures. In five subjects, pretreatment with the 5-HT receptor antagonist ketanserin before a second PET scan significantly decreased [C]Cimbi-36 binding in all cortical regions with no effects in cerebellum. These results confirm that [C]Cimbi-36 binding is selective for 5-HT receptors in the cerebral cortex and that cerebellum is an appropriate reference tissue for quantification of 5-HT receptors in the human brain. Thus, we here describe [C]Cimbi-36 as the first agonist PET radioligand to successfully image and quantify 5-HT receptors in the human brain.Journal of Cerebral Blood Flow & Metabolism advance online publication, 30 April 2014; doi:10.1038/jcbfm.2014.68.
Original languageEnglish
JournalJournal of Cerebral Blood Flow and Metabolism
Volume34
Pages (from-to)1188-1196
Number of pages9
ISSN0271-678X
DOIs
Publication statusPublished - 30 Apr 2014

ID: 111037056