DESENSITIZATION OF NICOTINE-STIMULATED RB-86(+) EFFLUX FROM MOUSE-BRAIN SYNAPTOSOMES

The desensitization of nicotine-stimulated Rb-86(+) efflux from synaptosomes prepared from C57BL/6 mouse brain was investigated. Nicotine stimulated a saturable, concentration-dependent efflux of Rb-86(+) from synaptosomes (EC(50) = 0.60 mu M), but the response decreased with time of exposure to nicotine. The rate of decrease of the response (desensitization) increased as the nicotine concentration was increased (EC(50) = 0.35 mu M; maximal rate of desensitization = 1.1 min(-1)). Desensitization of nicotine-stimulated Rb-86(+) efflux was also observed when synaptosomes were exposed to low (1-200 nM) concentrations of nicotine that caused little or no stimulation of efflux (EC(50) = 13 nM). The rate of desensitization observed with low nicotine concentrations (0.30 min(-1)) was less than that measured at stimulating concentrations. Desensitization was not fully reversible for synaptosomes exposed to nicotine concentrations between 10 nM and 10 mu M: Only 60-40% of the control response was regained after a 10-min washout period. The kinetics of functional desensitization were compared with the kinetics of [H-3]nicotine binding. [H-3]Nicotine binding to midbrain particulate fractions displayed both a fast and a slow phase. The EC(50) values for these two phases were 2.6 and 14 nM, respectively. Data obtained from functional desensitization and ligand binding experiments were analyzed using a two-state model. The kinetic constants obtained from the analyses of these two processes were very similar. Overall, the results suggest that nicotinic receptor function measured with ion flux desensitizes when exposed to either stimulating or nonstimulating concentrations of nicotine. In addition, the kinetic properties calculated for the functional desensitization are comparable to those for [H-3]nicotine binding.