LOCALIZATION OF RAT-BRAIN BINDING-SITES FOR [H-3] TOMOXETINE, AN ENANTIOMERICALLY PURE LIGAND FOR NOREPINEPHRINE REUPTAKE SITES

Citation
Dr. Gehlert et al., LOCALIZATION OF RAT-BRAIN BINDING-SITES FOR [H-3] TOMOXETINE, AN ENANTIOMERICALLY PURE LIGAND FOR NOREPINEPHRINE REUPTAKE SITES, Neuroscience letters, 157(2), 1993, pp. 203-206
Citations number
10
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
03043940
Volume
157
Issue
2
Year of publication
1993
Pages
203 - 206
Database
ISI
SICI code
0304-3940(1993)157:2<203:LORBF[>2.0.ZU;2-8
Abstract
The distribution of binding sites for the potent inhibitor of norepine phrine (NE) reuptake, [H-3]tomoxetine, was examined in rat brain using quantitative autoradiography. Scatchard analysis of [H-3]tomoxetine-b inding to slide-mounted sections of rat forebrain indicated that the l igand bound to two sites, a high-affinity site with a K(d) of 0.29 nM and a lower-affinity site with a K(d) of 16 nM. Pharmacological charac terization of this high-affinity site was consistent with labelling a NE-uptake site in brain. Autoradiographic localization of the binding sites for [H-3]tomoxetine was performed at a ligand concentration of 1 nM representing the distribution of high-affinity sites. The radiolig and bound with a distribution of binding sites that was consistent wit h the known distribution of NE-containing neurons. The highest levels of binding were seen in regions, such as the locus coeruleus, bed nucl eus of the stria terminalis, anterior ventral nucleus of the thalamus and the paraventricular nucleus of the hypothalamus. Low levels were s een in regions such as the caudate-putamen, ventral tegmental area and zona reticulata of the substantia nigra, where NE-containing neurons have been reported to be low. Binding to all these sites was inhibited by 1 muM desipramine which produced autoradiograms with a uniform non specific binding. These results indicate that low concentrations of [H -3]tomoxetine can be used to localize and characterize NE-binding site s. Further study will be necessary to determine the nature of the low- affinity binding site.