Jo_2002_J.Neurophysiol_88_2501

Reference

Title : Cholinergic modulation of purinergic and GABAergic co-transmission at in vitro hypothalamic synapses - Jo_2002_J.Neurophysiol_88_2501
Author(s) : Jo YH , Role LW
Ref : Journal of Neurophysiology , 88 :2501 , 2002
Abstract :

The lateral hypothalamus (LH) is an important center for the integration of autonomic and limbic information and is implicated in the modulation of visceral motor and sensory pathways, including those underlying feeding and arousal behaviors. LH neurons in vitro release both ATP and GABA. The control of ATP and GABA co-transmission in LH may underlie the participation of LH in basic aspects of arousal and reinforcement. LH neurons receive cholinergic input from the pedunculopontine and laterodorsal tegmental nuclei as well as from cholinergic interneurons within the LH per se. This study presents evidence for nicotinic acetylcholine receptor (nAChR)-mediated enhancement of GABAergic, but not of purinergic, transmission despite the co-transmission of ATP and GABA at LH synapses in vitro. Facilitation of GABAergic transmission by nicotine is inhibited by antagonists of (alphabeta)*-containing nAChRs, but is unaffected by an alpha7-selective antagonist, consistent with a nAChR-mediated enhancement of GABA release mediated by non-alpha7-containing nAChRs. Activation of muscarinic ACh receptors enhances the release of ATP while concomitantly depressing GABAergic transmission. The independent modulation of ATP/GABAergic transmission may provide a new level of synaptic flexibility in which individual neurons utilize more than one neurotransmitter but retain independent control over their synaptic activity.

PubMedSearch : Jo_2002_J.Neurophysiol_88_2501
PubMedID: 12424289

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Citations formats

Jo YH, Role LW (2002)
Cholinergic modulation of purinergic and GABAergic co-transmission at in vitro hypothalamic synapses
Journal of Neurophysiology 88 :2501

Jo YH, Role LW (2002)
Journal of Neurophysiology 88 :2501