Novel Ca2+ dependence and time course of somatodendritic dopamine release:Substantia nigra versus striatum

Somatodendritic release of dopamine (DA) in midbrain represents a novel for m of intercellular signaling that inherently differs from classic axon-term inal release. Here we report marked differences in the Ca2+ dependence and time course of stimulated increases in extracellular DA concentration ([DA] (o)) between the substantia nigra pars compacta (SNc) and striatum. Evoked [DA](o) was monitored with carbon-fiber microelectrodes and fast-scan cycli c voltammetry in brain slices. In striatum, pulse-train stimulation (10 Hz, 30 pulses) failed to evoke detectable [DA](o) in 0 or 0.5 mm Ca2+ but elic ited robust release in 1.5 mm Ca2+. Release increased progressively in 2.0 and 2.4 mm Ca2+. In sharp contrast, evoked [DA](o) in SNc was nearly half-m aximal in 0 mm Ca2+ and increased significantly in 0.5 mm Ca2+. Surprisingl y, somatodendritic release was maximal in 1.5 mm Ca2+ with no change in 2.0 or 2.4 mm Ca2+. Additionally, after single-pulse stimulation, evoked [DA]( o) in striatum reached a maximum (t(max)) in <200 msec, whereas in SNc, [DA ](o) continued to rise for 2-3 sec. Similarly, the time for [DA](o) to deca y to 50% of maximum (t(50)) was 12-fold longer in SNc than striatum. A dela yed t(max) in SNc compared with striatum persisted when DA uptake was inhib ited by GBR-12909 and D-2 autoreceptors were blocked by sulpiride, although these agents eliminated the difference in tc. Together, these data implica te different release mechanisms in striatum and SNc, with minimal Ca2+ requ ired to trigger prolonged DA release in SNc. Coupled with limited uptake, p rolonged somatodendritic release would facilitate DA-mediated volume transm ission in midbrain.