E. Hirani et al., Pindolol occupancy of 5-HT1A receptors measured in vivo using small animalpositron emission tomography with carbon-11 labeled WAY 100635, SYNAPSE, 36(4), 2000, pp. 330-341
Positron emission tomography (PET), following an intravenous injection of [
carbonyl-C-11]WAY 100635, was used to image central 5-HT1A receptors in rat
following pretreatment with graded doses of(-)-pindolol (0.001-3 mg/kg, i.
v.). The use of PET had advantages over ex vivo radioligand binding methods
in that it produced parametric image volumes and reduced errors due to int
er-rat variability. Time-radioactivity curves from regions of interest (ROI
) acquired from individual rats enabled the estimation of specific binding
of the radioligand using a compartmental model with reference tissue input.
Binding potential (BP) of [C-11]WAY 100635 was estimated for frontal corte
x and hippocampus (postsynaptic), and midbrain raphe nuclei (presynaptic).
In the latter ROI, pindolol dose-dependently decreased BP. The saturation c
urve could be fitted to a single-site model up to the lowest dose of pindol
ol used, giving an ED50 (dose to cause 50% occupancy) value of 0.26 +/- 0.0
5 mg/kg, and inclusion of control (nonpindolol-treated) rats did not affect
the fit. In contrast, in cortex and hippocampus ROI, low doses of pindolol
caused an increase in BP compared with controls. Pindolol doses greater th
an similar to 0.1 mg/kg, resulted in a dose-dependent decrease in BP, and E
D50 values in cortex and hippocampus were estimated as 0.44 +/- 0.13 and 0.
48 +/- 0.12 mg/kg, respectively. The increase in [C-11]WAY 100635 binding a
t low pindolol doses is feasibly related to a decrease in basal receptor oc
cupancy following reduced release of endogenous 5-HT. Considering the appar
ently greater potency of pindolol at the midbrain raphe ROI, this effect co
uld be mediated via agonist activity at the autoreceptor. Synapse 36:330-34
1, 2000. (C) 2000 Wiley-Liss, Inc.