Nicotinic receptor binding sites in rat primary neuronal cells in culture:characterization and their regulation by chronic nicotine

We have characterized high affinity neuronal nicotinic acetylcholine recept ors labeled by [H-3]cytisine in primary neuronal cell cultures from fetal r at brains. After 15 days in culture, the highest density of [H-3]cytisine b inding sites (B-max approximate to 57 fmol/mg protein) was found in cells f rom the brainstem, which includes the following subcortical brain areas: th e septum, thalamus, hypothalamus, midbrain, pens and medulla. A lower densi ty of sites was found in cells from the cerebral cortex, hippocampus, and c audate nucleus. [H-3]Cytisine binds to receptors in primary cells from the brainstem and cerebral cortex with a K-d of approximate to 0.5 nM, and the binding is inhibited by the agonists nicotine, acetylcholine, and epibatidi ne with IC50 values of 1 to 20 nM, and by carbachol and the antagonist dihy dro-beta-erythroidine with IC50 values of 0.5 to 1.5 mu M. Chronic treatmen t of neuronal cultures with nicotine for 7 days differentially affected the number of nicotinic receptors in cells from different brain areas; it sign ificantly increased the number of nicotinic binding sites in cells from the cerebral cortex, hippocampus, and caudate, but not in cells from the brain stem. The nicotine-induced increase of receptors in cerebral cortical cultu res was not blocked by either mecamylamine or dihydro-beta-erythroidine. Th ese results indicate that primary cultures of rat neuronal cells provide a good model system in which to study and compare the properties and regulati on of native neuronal nicotinic acetylcholine receptors. (C) 1999 Elsevier Science B.V. All rights reserved.