Dual projections of single cholinergic and aminergic brainstem neurons to the thalamus and basal forebrain in the rat

Bruno J. Losier, Kazue Semba

Résultat de recherche: Articleexamen par les pairs

101 Citations (Scopus)

Résumé

Compelling evidence indicates that cholinergic basal forebrain neurons are strongly activated during waking, and concurrently thalamic spindle activity is suppressed and thalamocortical sensory transmission is facilitated. Both thalamus and basal forebrain are known to receive projections from brainstem cholinergic and aminergic neuronal pools that are involved in wake/sleep regulation. The present study addressed the question of whether single cholinergic and aminergic neurons contributed to both of these ascending projections, by using two fluorescent retrograde tracers combined with immunoflurrescence. Cholinergic neurons projecting to both the basal forebrain and thalamus were found in the pedunculopontine and laterodorsal tegmental nuclei, representing an average of 8.0% of the total cholinergic cell population in these nuclei. Serotonergic neurons with dual projections were observed in the dorsal, median and caudal linear raphe nuclei, accounting for a mean of 4.7% of total serotonergic nerrons in these nuclei. Relatively few noradrenergic neurons (2.0%) in the locus ceruleus projected to both target structures, and a very small subpopulation of histaminergic neurons (1.5%) in the tuberomammillary hypothalamic nucleus had dual projections. Of all brainstem neurons with dual projections, cholinergic and serotonergic neurons accounted for an overwhelming majority, with noradrenergic followed by histaminergic neurons representing the remaining minority. These data suggest that through dual projections, cholinergic and aminnrgic brainstem neurons can concurrently modulate the activity of neurons in the thalamus and basal forebrain during cortical arousal.

Langue d'origineEnglish
Pages (de-à)41-52
Nombre de pages12
JournalBrain Research
Volume604
Numéro de publication1-2
DOI
Statut de publicationPublished - févr. 26 1993

Note bibliographique

Funding Information:
ChAT choline acetyltransferase FG Fluorogold FITC fiuorescein isothiocyanate HDC histidine decarboxylase 5-HT 5-hydroxytryptamine (serotonin) PB phosphate buffer REM rapid eye movement Rh rhodamine latex beads TBS Tris-buffered saline TH tyrosine hydroxylase Acknowledgements. The authors thank Dr. N. Inagaki for a generous gift of the antisera histidine decarboxylase, Dr. Doug Rasmusson for a critical reading of an early version of the manuscript, and Ms. Janette Nason and Ms. Joan Burns for excellent technical assistance. The work was supported by the Medical Research Council, Alzheimer Society, and Scottish Rite Charitable Foundation of Canada. B.J.L. is a recipient of a Medical Research Council Studentship Award, and K.S. is an MRC Scholar.

ASJC Scopus Subject Areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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