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Abstract
The effects of a single rapid-rate transcranial magnetic stimulation (rTMS) exposure
on neurotransmitter binding sites in the rat brain 24 h after the stimulation were
examined. Quantification by in vitro-autoradiography showed no differences for 3H-paroxetine
binding (5-HT uptake sites) between rTMS-treated, sham and control animals. In contrast,
the number of 5-HT1A binding sites (labeled with 3H-8-OH-DPAT) were selectively increased
in the rTMS-group with significantly higher BMAX values in the frontal cortex, the
cingulate cortex, and the anterior olfactory nucleus. A non-specific increase in NMDA
binding sites (labeled with 125I-MK-801) in rTMS and sham animals was observed in
the hippocampal formation. A selective increase of these binding sites after rTMS
was detected in the ventromedial hypothalamus, the basolateral amygdala and layers
5-6 of the parietal cortex. These findings imply that a single rTMS exposure can result
in persistent effects on NMDA and 5-HT1A binding sites even 24 h after stimulation
and therefore may be of relevance with respect to the therapeutic action of rTMS reported
from clinical studies.
Copyright 1999 Elsevier Science B.V.