Imaging the norepinephrine transporter in humans with ( S , S )-[11 C] O -methyl reboxetine and PET: problems and progress

• Published in: Nuclear medicine and biology 2007-08, Vol.34 (6), p.667-679
• Main Authors: Logan, Jean, Wang, Gene-jack, Telang, Frank, Fowler, Joanna S, Alexoff, David, Zabroski, John, Jayne, Millard, Hubbard, Barbara, King, Payton, Carter, Pauline, Shea, Colleen, Xu, Youwen, Muench, Lisa, Schlyer, David, Learned-Coughlin, Susan, Cosson, Valerie, Volkow, Nora D, Ding, Yu-shin
• Format: Article
• Language: English
• Subjects: [ 11C]( S, S)-MRB; Adrenergic Uptake Inhibitors - pharmacokinetics; Adrenergic Uptake Inhibitors - pharmacology; Adult; Algorithms; Atomoxetine; Atomoxetine Hydrochloride; Brain - diagnostic imaging; Carbon Radioisotopes; Data Interpretation, Statistical; Dose-Response Relationship, Drug; Humans; Image Processing, Computer-Assisted; Male; Morpholines - blood; Morpholines - pharmacokinetics; Norepinephrine Plasma Membrane Transport Proteins - antagonists & inhibitors; Norepinephrine Plasma Membrane Transport Proteins - metabolism; Norepinephrine transporter; PET; Positron-Emission Tomography; Propylamines - pharmacokinetics; Propylamines - pharmacology; Radiology; Radiopharmaceuticals - blood; Radiopharmaceuticals - pharmacokinetics; Reproducibility of Results
• ISSN: 0969-8051; 1872-9614
• DOI: 10.1016/j.nucmedbio.2007.03.013

Abstract Results from human studies with the PET radiotracer ( S , S )-[11 C] O -methyl reboxetine ([11 C]( S , S )-MRB), a ligand targeting the norepinephrine transporter (NET), are reported. Quantification methods were determined from test/retest studies, and sensitivity to pharmacological blockade was tested with different doses of atomoxetine (ATX), a drug that binds to the NET with high affinity ( Ki =2–5 nM). Methods Twenty-four male subjects were divided into different groups for serial 90-min PET studies with [11 C]( S , S )-MRB to assess reproducibility and the effect of blocking with different doses of ATX (25, 50 and 100 mg, po). Region-of-interest uptake data and arterial plasma input were analyzed for the distribution volume (DV). Images were normalized to a template, and average parametric images for each group were formed. Results [11 C]( S , S )-MRB uptake was highest in the thalamus (THL) and the midbrain (MBR) [containing the locus coeruleus (LC)] and lowest for the caudate nucleus (CDT). The CDT, a region with low NET, showed the smallest change on ATX treatment and was used as a reference region for the DV ratio (DVR). The baseline average DVR was 1.48 for both the THL and MBR with lower values for other regions [cerebellum (CB), 1.09; cingulate gyrus (CNG) 1.07]. However, more accurate information about relative densities came from the blocking studies. MBR exhibited greater blocking than THL, indicating a transporter density ∼40% greater than THL. No relationship was found between DVR change and plasma ATX level. Although the higher dose tended to induce a greater decrease than the lower dose for MBR (average decrease for 25 mg=24±7%; 100 mg=31±11%), these differences were not significant. The different blocking between MBR (average decrease=28±10%) and THL (average decrease=17±10%) given the same baseline DVR indicates that the CDT is not a good measure for non-NET binding in both regions. Threshold analysis of the difference between the average baseline DV image and the average blocked image showed the expected NET distribution with the MBR (LC) and hypothalamus>THL>CNG and CB, as well as a significant change in the supplementary motor area. DVR reproducibility for the different brain regions was ∼10%, but intersubject variability was large. Conclusions The highest density of NETs was found in the MBR where the LC is located, followed by THL, whereas the lowest density was found in basal ganglia (lowest in CDT), consistent with the