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Synthesis and Characterization of Binding of 5-[76Br] Bromo-3-[[2(S)-Azetidinyl]methoxy]pyridine, a Novel Nicotinic Acetylcholine Receptor Ligand, in Rat Brain
Authors:Wiebke Sihver†  Karl-Johan Fasth  rew G Horti†  rei O Koren†  Mats Bergström  Li Lu  Gisela Hagberg  Hans Lundqvist§  Robert F Dannals†  Edythe D London†  Agneta Nordberg&#;  & Bengt Långström
Institution:PET Centre Uppsala University, Sweden.
Abstract:5-76Br]Bromo-3-2(S)-azetidinyl]methoxy]pyridine (76Br]BAP), a novel nicotinic acetylcholine receptor ligand, was synthesized using 76Br]bromide in an oxidative bromodestannylation of the corresponding trimethylstannyl compound. The radiochemical yield was 25%, and the specific radioactivity was on the order of 1 Ci/micromol. The binding properties of 76Br]BAP were characterized in vitro and in vivo in rat brain, and positron emission tomography (PET) experiments were performed in two rhesus monkeys. In association experiments on membranes of the cortex and thalamus, >90% of maximal specific 76Br]BAP binding was obtained after 60 min. The dissociation half-life of 76Br]BAP was 51 +/- 6 min in cortical membranes and 56 +/- 3 min in thalamic membranes. Saturation experiments with 76Br]BAP revealed one population of binding sites with dissociation constant (K(D)) values of 36 +/- 9 and 30 +/- 9 pM in membranes of cortex and thalamus, respectively. The maximal binding site density (Bmax) values were 90 +/- 17 and 207 +/- 33 fmol/mg in membranes of cortex and thalamus, respectively. Scatchard plots were nonlinear, and the Hill coefficients were <1, suggesting the presence of a lower-affinity binding site. In vitro autoradiography studies showed that binding of 76Br]BAP was high in the thalamus and presubiculum, moderate in the cortex and striatum, and low in the cerebellum and hippocampus. A similar pattern of 76Br]BAP accumulation was observed by ex vivo autoradiography. In vivo, binding of 76Br]BAP in whole rat brain was blocked by preinjection of (S)(-)-nicotine (0.3 mg/kg) by 27, 52, 68, and 91% at survival times of 10, 25, 40, 120, and 300 min, respectively. In a preliminary PET study in rhesus monkeys, the highest 76Br]BAP uptake was found in the thalamus, and radioactivity was displaceable by approximately 60% with cytisine and by 50% with (S)(-)-nicotine. The data of this study indicate that 76Br]BAP is a promising radioligand for the characterization of nicotinic acetylcholine receptors in vivo.
Keywords:5-[76Br]Bromo-3-[[2(S)-azetidinyl]methoxy]pyridine  Nicotinic receptor binding  In vitro studies  In vivo studies  Positron emission tomography
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