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
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.