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Journal of Psychopharmacology
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0269881106071975v1
21/6/628    most recent
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Article

Ecstasy-induced reduction of the availability of the brain serotonin transporter as revealed by [11C](+)McN5652-PET and the multi-linear reference tissue model: loss of transporters or artifact of tracer kinetic modelling?

R. Buchert1*, Frank Thiele2, Rainer Thomasius3, Florian Wilke1, Kay Petersen3, Winfried Brenner1, Janos Mester1, Lothar Spies2, Malte Clausen1

1 Department of Nuclear Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
2 Philips Research Laboratories Aachen, Aachen, Germany.
3 Department of Psychiatry and Psychotherapy, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

* To whom correspondence should be addressed.


   Abstract

In a previous positron emission tomography (PET) study with the serotonin transporter (SERT) ligand [11C](+)McN5652, we found protracted reduction of the availability of the brain SERT in users of the drug ecstasy. However, the multi-linear reference tissue method for the quantification of SERT availability used in this study is prone to effects of altered levels of statistical noise that could simulate reduction of SERT. The aim of the present study was to take into account this confound by re-evaluation of the data now using a modelling approach that is rather insensitive to alterations in the level of statistical noise. A total of 116 subjects (30 current, 29 former ecstasy users, 29 drug-naive, 28 polydrug controls) in whom [11C](+)McN5652-PET had been performed previously were re-evaluated. The equilibrium specific-to-non-specific partition coefficient V3 was obtained voxel-wise by application of the simplified reference tissue method (SRTM), which provides quite unbiased results up to rather large noise levels. Voxel-based comparisons between the groups were performed using statistical parametric mapping. V3 was reduced in the striatum and in the thalamus in current ecstasy users. This was confirmed by volume-of-interest-based analysis. This result suggests that the ecstasy-induced reduction of SERT availability in SERT-rich brain regions reported previously indicates reduced SERT binding potential rather than being an artifact of tracer kinetic modelling. SRTM analysis did not confirm previous findings in neocortical brain areas.

Key Words: ecstasy, serotonin transporter, PET, (+)McN5652, simplified reference tissue method, multi-linear reference tissue method

First published on November 8, 2006, doi:10.1177/0269881106071975

Journal of Psychopharmacology 2007;21:628.

A more recent version of this article appeared on August 1, 2007


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