期刊
JOURNAL OF NEUROSCIENCE
卷 21, 期 19, 页码 7841-7847出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.21-19-07841.2001
关键词
calcium; dopamine; dopamine transporter; substantia nigra pars compacta; voltammetry; volume transmission; synaptic transmission
资金
- NINDS NIH HHS [NS-36362] Funding Source: Medline
Somatodendritic release of dopamine (DA) in midbrain represents a novel form of intercellular signaling that inherently differs from classic axon-terminal 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 cyclic 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 elicited 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-maximal in 0 mm Ca2+ and increased significantly in 0.5 mm Ca2+. Surprisingly, 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 decay to 50% of maximum (t(50)) was 12-fold longer in SNc than striatum. A delayed t(max) in SNc compared with striatum persisted when DA uptake was inhibited by GBR-12909 and D-2 autoreceptors were blocked by sulpiride, although these agents eliminated the difference in tc. Together, these data implicate different release mechanisms in striatum and SNc, with minimal Ca2+ required to trigger prolonged DA release in SNc. Coupled with limited uptake, prolonged somatodendritic release would facilitate DA-mediated volume transmission in midbrain.
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