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Neurotensin-Induced Bursting of Cholinergic Basal Forebrain Neurons Promotes γ and θ Cortical Activity Together with Waking and Paradoxical Sleep

Authors :
Ian D. Manns
Barbara E. Jones
Edmund G. Cape
Alain Beaudet
Angel Alonso
Source :
The Journal of Neuroscience. 20:8452-8461
Publication Year :
2000
Publisher :
Society for Neuroscience, 2000.

Abstract

Cholinergic basal forebrain neurons have long been thought to play an important role in cortical activation and behavioral state, yet the precise way in which they influence these processes has yet to be fully understood. Here, we have examined the effects on the electroencephalogram (EEG) and sleep–wake state of basal forebrain administration of neurotensin (NT), a neuropeptide that has been shownin vitroto potently and selectively modulate the cholinergic cells. Microinjection of (0.1–3.0 mm) NT into the basal forebrain of freely moving, naturally waking-sleeping rats produced a dose-dependent decrease in δ (∼1–4 Hz) and increase in both θ (∼4–9 Hz) and high-frequency γ activity (30–60 Hz) across cortical, areas with no increase in the electromyogram. These EEG changes were accompanied by concomitant decreases in slow wave sleep (SWS) and transitional SWS (tSWS), increases in wake, and most remarkably, increases in paradoxical sleep (PS) and transitional PS (tPS), despite the virtual absence of SWS. The effects were attributed to direct action on cholinergic neurons as evidenced by selective internalization of a fluorescent ligand, Fluo-NT, in choline acetyltransferase (ChAT)-immunoreactive cells and stimulation by NT of bursting discharge in juxtacellularly recorded, Neurobiotin-labeled, ChAT-immunoreactive neurons. We conclude that NT-induced rhythmic bursting of cholinergic basal forebrain neurons stimulates rhythmic θ oscillations and γ across the cerebral cortex. With the selective action of NT on the cholinergic cells, their bursting discharge promotes θ and γ independent of motor activity and thereby also stimulates and enhances PS.

Details

ISSN :
15292401 and 02706474
Volume :
20
Database :
OpenAIRE
Journal :
The Journal of Neuroscience
Accession number :
edsair.doi.dedup.....81aa0c826a7302dc0a16414936044f58