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Sleep-Active Neuronal Nitric Oxide Synthase-Positive Cells of the Cerebral Cortex: A Local Regulator of Sleep?
Author(s) -
Jonathan P. Wisor,
Dmitry Gerashchenko,
Thomas S. Kilduff
Publication year - 2011
Publication title -
current topics in medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.706
H-Index - 116
eISSN - 1873-4294
pISSN - 1568-0266
DOI - 10.2174/156802611797470367
Subject(s) - regulator , sleep (system call) , cerebral cortex , nitric oxide synthase , nitric oxide , neuronal nitric oxide synthase , neuroscience , cortex (anatomy) , chemistry , atp synthase , medicine , biology , enzyme , biochemistry , gene , computer science , operating system
Our recent report demonstrated that a small subset of GABAergic interneurons in the cerebral cortex of rodents expresses Fos protein, a marker for neuronal activity, during SWS [1]. The population of sleep-active neurons consists of strongly immunohistochemically-stained cells for the enzyme neuronal nitric oxide synthase (Type I cells). By virtue of their widespread localization within the cerebral cortex and their widespread projections to other cortical cell types, cortical neuronal nitric oxide synthase-positive neurons are positioned to play a central role in the local regulation of sleep waveforms within the cerebral cortex. Here, we review the possible functions of neuronal nitric oxide synthase and its diffusible gas product, nitric oxide, in regulating neuronal activity, synaptic plasticity and cerebral blood flow within the context of local sleep regulation in the cerebral cortex. We also summarize what is known, in addition to their expression of neuronal nitric oxide synthase, about the biochemical phenotype, synaptic connectivity and electrophysiological properties of this novel sleep-active population of cells. Finally, we raise some critical unanswered questions about the role of this population in local sleep regulation within the cerebral cortex and describe some experimental approaches that might be used to address those questions.

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