Molecular and physiological diversity of nicotinic acetylcholine receptorsin the midbrain dopaminergic nuclei

Nicotinic acetylcholine receptors (nAChRs) on dopaminergic (DA) and GABAerg ic (Gaba) projection neurons of the substantia nigra (SN) and ventral tegme ntal area (VTA) are characterized by single-cell RT-PCR and patch-clamp rec ordings in slices of rat and wild-type, beta2-/-, alpha4-/-, and alpha7-/- mice. The eight nAChR subunits expressed in these nuclei, alpha3-7 and beta 2-4, contribute to four different types of nAChR-mediated currents. Most DA neurons in the SN and VTA express two nAChR subtypes. One is inhibited by dihydro-beta -erythroidine (2 muM), alpha -conotoxin MII (10 nM), and methy llycaconitine (1 nM) but does not contain the alpha7 subunit; it possesses a putative alpha4 alpha6 alpha5(beta2)(2) composition. The other subtype is inhibited by dihydro-beta -erythroidine (2 muM) and has a putative alpha4 alpha5(beta2)(2) composition. Gaba neurons in the VTA exhibit a third subty pe with a putative (alpha4)(2)(beta2)(3) composition, whereas Gaba neurons in the SN have either the putative (alpha4)(2)(beta2)(3) oligomer or the pu tative alpha4 alpha6 alpha5(beta2)(2) oligomer. The fourth subtype, a putat ive (alpha7)(5) homomer, is encountered in less than half of DA and Gaba ne urons, in the SN as well as in the VTA. Neurons in the DA nuclei thus exhib it a diversity of nAChRs that might differentially modulate reinforcement a nd motor behavior.