@article {Momiyama7505, author = {Toshihiko Momiyama and J. A. Sim}, title = {Modulation of Inhibitory Transmission by Dopamine in Rat Basal Forebrain Nuclei: Activation of Presynaptic D1-like Dopaminergic Receptors}, volume = {16}, number = {23}, pages = {7505--7512}, year = {1996}, doi = {10.1523/JNEUROSCI.16-23-07505.1996}, publisher = {Society for Neuroscience}, abstract = {The effects of dopamine (DA) on inhibitory transmission onto identified magnocellular neurons were examined in rat basal forebrain slices using whole-cell recording. IPSCs evoked by focal stimulation within basal forebrain nuclei were reversibly blocked by 10 μm bicuculline and had a decay time constant of 20.1 {\textpm} 0.77 msec in the presence of 6-cyano-7-nitroquinoxalline-2,3-dione (5 μm). Bath application of DA reduced the amplitude of IPSCs up to 71.1 {\textpm} 1.49\% in a concentration-dependent manner between 0.003 and 1 mm (the IC50 value being 6.6 μm), without any effect on the holding current at -70 mV. DA (10 μm) reduced the frequency of miniature IPSCs (mIPSCs) recorded in the presence of TTX (0.5 μm), without affecting their mean amplitude, rise time, and decay time constant. Furthermore, the DA-induced effect on mIPSCs remained unaffected by 100 μm cadmium, suggesting a presynaptic mechanism independent of calcium influx. SKF 81297, a D1-like agonist, mimicked DA-induced effect on evoked IPSCs (IC50, 10.9 μm), whereas R(-)-TNPA or (-)-quinpirole, D2-like agonists (30 μm), had little or no effect on the amplitude of evoked IPSCs. R(+)-SCH 23390, a D1-like antagonist, antagonized the DA-induced effect on IPSCs (KB 0.82 μm), whereas S(-)-eticlopride, a D2-like antagonist, showed slight antagonism (KB 7.8 μm). Forskolin (10 μm) reduced the amplitude of evoked IPSCs to \~{}58\% of the control and occluded the inhibitory effect of DA. These findings indicate that DA reduces inhibitory transmission onto magnocellular basal forebrain neurons by activating presynaptic D1-like receptors.}, issn = {0270-6474}, URL = {https://www.jneurosci.org/content/16/23/7505}, eprint = {https://www.jneurosci.org/content/16/23/7505.full.pdf}, journal = {Journal of Neuroscience} }