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Characterization of the novel GlyT1 PET tracer [ 18 F]MK‐6577 in humans
Author(s) -
Joshi Aniket D.,
SanabriaBohórquez Sandra M.,
Bormans Guy,
Koole Michel,
Hoon Jan,
Hecken Anne,
Depre Marleen,
Lepeleire Inge,
Laere Koen,
Sur Cyrille,
Hamill Terence G.
Publication year - 2015
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.21782
Subject(s) - reuptake , glutamatergic , nuclear medicine , effective dose (radiation) , in vivo , positron emission tomography , chemistry , binding potential , schizophrenia (object oriented programming) , pharmacology , neuroscience , medicine , glutamate receptor , receptor , psychology , biology , biochemistry , serotonin , microbiology and biotechnology , psychiatry
Decreased glutamatergic neurotransmission is hypothesized to be involved in the pathophysiology of schizophrenia. Inhibition of glycine transporter Type‐1 (GlyT1) reuptake is expected to increase the glutamatergic neurotransmission and may serve as treatment for cognitive and negative symptoms of schizophrenia. In this article, we present human data from a novel GlyT1 PET tracer, [ 18 F]MK‐6577. In the process of developing a GlyT1 inhibitor therapeutic, a PET tracer can assist in determining the dose with a high probability of sufficiently testing the mechanism of action. This article reports the human PET studies with [ 18 F]MK‐6577 for measuring GlyT1 receptor availability at baseline in normal human subjects and occupancy with a GlyT1 inhibitor, MK‐2637. Studies were also performed to measure radiation burden and the baseline test‐retest (T‐RT) variability of the tracer. The effective dose from sequential whole‐body dosimetry scans in three male subjects was estimated to be 24.5 ± 2.9 µSV/MBq (mean ± SD). The time–activity curves from T‐RT scans modeled satisfactorily using a two tissue compartmental model. The tracer uptake was highest in the pons (V T = 6.7 ± 0.9, BP ND = 4.1 ± 0.43) and lowest in the cortex (V T = 2.1 ± 0.5, BP ND = 0.60 ± 0.23). V T T‐RT variability measured in three subjects was <12% on average. The occupancy scans performed in a cohort of 15 subjects indicated absence of a reference region. The in vivo potency (Occ 50 ) of MK‐2637 was determined using two methods: A: Lassen plot with a population input function (Occ 50 = 106 nM, SE = 20 nM) and B: pseudo reference tissue model using cortex as the pseudo reference region (Occ 50 = 141 nM, SE = 21 nM). Synapse 69:33–40, 2015. © 2014 Wiley Periodicals, Inc.