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J Neurophysiol 92: 433-443, 2004. First published February 11, 2004; doi:10.1152/jn.00543.2003
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Opposing Electrophysiological Actions of 5-HT on Noncholinergic and Cholinergic Neurons in the Rat Ventral Pallidum In Vitro

C. Peter Bengtson1, David J. Lee2 and Peregrine B. Osborne1,3

1Department of Physiology and Pharmacology, School of Biomedical Sciences, The University of Queensland, Brisbane; 2Pain Management Research Institute, University of Sydney at Royal North Shore Hospital, St Leonards NSW 2065, Sydney; and 3Prince of Wales Medical Research Institute and the University of New South Wales, Sydney, Australia

Submitted 4 June 2003; accepted in final form 6 February 2004

The ventral pallidum in rat is a basal forebrain structure that contains neurons that project in the limbic striatopallidal circuitry and magnocellular cholinergic corticopetal neurons. Because 5-hydroxytryptamine (5-HT) terminals on dorsal raphe projections form close appositions with these neurons, we made patch-clamp recordings in immature rat brain slices to determine whether they are modulated by postsynaptic 5-HT receptors. Inward currents were predominantly induced by 5-HT in noncholinergic neurons, which were distinguished from cholinergic neurons by immunohistochemical and electrophysiological criteria. The inward current induced by 5-HT was mimicked and occluded when adenylyl cyclase was stimulated with forskolin, and was almost abolished when h-currents in noncholinergic neurons were blocked with cesium. Consistent with 5-HT7 receptor activation of h-curents by cAMP in other brain regions, we found inward currents were mimicked by the mixed 5-HT1/5-HT7 agonists 5-methoxytryptamine, and by 5-carboxamidotryptamine (5-CT), which was more potent than 5-HT. In contrast, 5-HT1 preferring 8-OH-DPAT was a weak partial agonist, and the 5-HT1–selective antagonist pindolol had no effect. However, despite this profile, antagonists that bind at the 5-HT7 receptor only partly reduced the agonist inward current (SB-269970 and clozapine), or had no effect (mianserin and pimozide). We found in cholinergic neurons that 5-HT predominantly induced hyperpolarizing currents, which were carried by potassium channels, and were smaller than currents induced by 8-OH-DPAT and 5-CT. We conclude from this study that ascending 5-HT projections from the dorsal raphe could have direct and opposite effects on the activities of neurons within the limbic striatopallidal and cholinergic corticopetal circuitry in the ventral pallidum.


Address for reprint requests and other correspondence: P. Osborne, Pain Management Research Institute, University of Sydney, Royal North Shore Hospital, St Leonards NSW 2065, Australia (E-mail p.osborne{at}usyd.edu.au).




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