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Alpha 2 adrenergic receptors on GABAergic, putative sleep‐promoting basal forebrain neurons
Author(s) -
Manns Ian D.,
Lee Maan Gee,
Modirrousta Mandana,
Hou Yiping P.,
Jones Barbara E.
Publication year - 2003
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.1460-9568.2003.02788.x
Subject(s) - basal forebrain , gabaergic , neuroscience , locus coeruleus , cholinergic neuron , substantia innominata , nucleus basalis , glutamate decarboxylase , cholinergic , forebrain , biology , slow wave sleep , nucleus accumbens , medicine , endocrinology , nucleus , inhibitory postsynaptic potential , dopamine , central nervous system , electroencephalography , biochemistry , enzyme
The basal forebrain plays an important role in the modulation of cortical activity and sleep‐wake states. Yet its role must be multivalent as lesions reportedly diminish cortical fast activity and also cortical slow activity along with slow wave sleep (SWS). Basal forebrain cholinergic vs. GABAergic cell groups could differentially influence these processes. By labelling recorded neurons with Neurobiotin (Nb) using the juxtacellular technique and identifying them by immunostaining, we previously found that whereas all cholinergic cells increased their firing, the majority of GABAergic neurons decreased their firing in association with evoked cortical activation in urethane‐anaesthetized rats. Here, we examined the possibility that such GABAergic, cortical activation ‘off’ cells might bear alpha 2 adrenergic receptors (α 2 AR) through which noradrenaline (NA) could inhibit them during cortical activation. First using simple dual‐immunostaining for glutamic acid decarboxylase (GAD) and the α 2A AR, we found that the majority (≈60%) of GAD‐immunopositive (GAD+) neurons through the magnocellular preoptic nucleus (MCPO) and substantia innominata (SI) were labelled for the α 2A AR. Second, in urethane‐anaesthetized rats, we examined whether Nb‐labelled, GAD+ cortical activation ‘off’ neurons that discharged maximally in association with cortical slow wave activity, were immunopositive for α 2A AR. We found that all the Nb+/GAD+‘off’ cells were labelled for the α 2A AR. Such cells could be inhibited in association with cortical activation and waking when noradrenergic locus coeruleus (LC) neurons discharge and be disinhibited with cortical slow waves and SWS when these neurons become inactive. We thus propose that α 2 AR‐bearing GABAergic basal forebrain neurons constitute sleep‐active and sleep‐promoting neurons.