Cholinergic neurons of the basal forebrain mediate biochemical and electrophysiological mechanisms underlying sleep homeostasis.

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Title: Cholinergic neurons of the basal forebrain mediate biochemical and electrophysiological mechanisms underlying sleep homeostasis.
Authors: Kalinchuk, Anna V., Porkka-Heiskanen, Tarja, McCarley, Robert W., Basheer, Radhika
Source: European Journal of Neuroscience. Jan2015, Vol. 41 Issue 2, p182-195. 14p.
Subjects: Cholinergic mechanisms, Neurons, Prosencephalon, Biochemistry, Electrophysiology, Homeostasis, Nitric-oxide synthases
Abstract: The tight coordination of biochemical and electrophysiological mechanisms underlies the homeostatic sleep pressure ( HSP) produced by sleep deprivation ( SD). We have reported that during SD the levels of inducible nitric oxide synthase (i NOS), extracellular nitric oxide ( NO), adenosine [ AD]ex, lactate [ Lac]ex and pyruvate [ Pyr]ex increase in the basal forebrain ( BF). However, it is not clear whether all of them contribute to HSP leading to increased electroencephalogram ( EEG) delta activity during non-rapid eye movement ( NREM) recovery sleep ( RS) following SD. Previously, we showed that NREM delta increase evident during RS depends on the presence of BF cholinergic ( Ch BF) neurons. Here, we investigated the role of Ch BF cells in coordination of biochemical and EEG changes seen during SD and RS in the rat. Increases in low-theta power (5-7 Hz), but not high-theta (7-9 Hz), during SD correlated with the increase in NREM delta power during RS, and with the changes in nitrate/nitrite [ NOx]ex and [ AD]ex. Lesions of Ch BF cells using Ig G 192-saporin prevented increases in [ NOx]ex, [ AD]ex and low-theta activity, during SD, but did not prevent increases in [ Lac]ex and [ Pyr]ex. Infusion of NO donor DETA NONOate into the saporin-treated BF failed to increase NREM RS and delta power, suggesting Ch BF cells are important for mediating NO homeostatic effects. Finally, SD-induced i NOS was mostly expressed in Ch BF cells, and the intensity of iNOS induction correlated with the increase in low-theta activity. Together, our data indicate ChBF cells are important in regulating the biochemical and EEG mechanisms that contribute to HSP. [ABSTRACT FROM AUTHOR]
Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Cholinergic neurons of the basal forebrain mediate biochemical and electrophysiological mechanisms underlying sleep homeostasis.
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  Data: <searchLink fieldCode="AR" term="%22Kalinchuk%2C+Anna+V%2E%22">Kalinchuk, Anna V.</searchLink><br /><searchLink fieldCode="AR" term="%22Porkka-Heiskanen%2C+Tarja%22">Porkka-Heiskanen, Tarja</searchLink><br /><searchLink fieldCode="AR" term="%22McCarley%2C+Robert+W%2E%22">McCarley, Robert W.</searchLink><br /><searchLink fieldCode="AR" term="%22Basheer%2C+Radhika%22">Basheer, Radhika</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Neuroscience%22">European Journal of Neuroscience</searchLink>. Jan2015, Vol. 41 Issue 2, p182-195. 14p.
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  Data: <searchLink fieldCode="DE" term="%22Cholinergic+mechanisms%22">Cholinergic mechanisms</searchLink><br /><searchLink fieldCode="DE" term="%22Neurons%22">Neurons</searchLink><br /><searchLink fieldCode="DE" term="%22Prosencephalon%22">Prosencephalon</searchLink><br /><searchLink fieldCode="DE" term="%22Biochemistry%22">Biochemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Electrophysiology%22">Electrophysiology</searchLink><br /><searchLink fieldCode="DE" term="%22Homeostasis%22">Homeostasis</searchLink><br /><searchLink fieldCode="DE" term="%22Nitric-oxide+synthases%22">Nitric-oxide synthases</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: The tight coordination of biochemical and electrophysiological mechanisms underlies the homeostatic sleep pressure ( HSP) produced by sleep deprivation ( SD). We have reported that during SD the levels of inducible nitric oxide synthase (i NOS), extracellular nitric oxide ( NO), adenosine [ AD]ex, lactate [ Lac]ex and pyruvate [ Pyr]ex increase in the basal forebrain ( BF). However, it is not clear whether all of them contribute to HSP leading to increased electroencephalogram ( EEG) delta activity during non-rapid eye movement ( NREM) recovery sleep ( RS) following SD. Previously, we showed that NREM delta increase evident during RS depends on the presence of BF cholinergic ( Ch BF) neurons. Here, we investigated the role of Ch BF cells in coordination of biochemical and EEG changes seen during SD and RS in the rat. Increases in low-theta power (5-7 Hz), but not high-theta (7-9 Hz), during SD correlated with the increase in NREM delta power during RS, and with the changes in nitrate/nitrite [ NOx]ex and [ AD]ex. Lesions of Ch BF cells using Ig G 192-saporin prevented increases in [ NOx]ex, [ AD]ex and low-theta activity, during SD, but did not prevent increases in [ Lac]ex and [ Pyr]ex. Infusion of NO donor DETA NONOate into the saporin-treated BF failed to increase NREM RS and delta power, suggesting Ch BF cells are important for mediating NO homeostatic effects. Finally, SD-induced i NOS was mostly expressed in Ch BF cells, and the intensity of iNOS induction correlated with the increase in low-theta activity. Together, our data indicate ChBF cells are important in regulating the biochemical and EEG mechanisms that contribute to HSP. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1111/ejn.12766
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        Text: English
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      – SubjectFull: Cholinergic mechanisms
        Type: general
      – SubjectFull: Neurons
        Type: general
      – SubjectFull: Prosencephalon
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      – SubjectFull: Biochemistry
        Type: general
      – SubjectFull: Electrophysiology
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      – SubjectFull: Homeostasis
        Type: general
      – SubjectFull: Nitric-oxide synthases
        Type: general
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      – TitleFull: Cholinergic neurons of the basal forebrain mediate biochemical and electrophysiological mechanisms underlying sleep homeostasis.
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            NameFull: Kalinchuk, Anna V.
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            NameFull: Porkka-Heiskanen, Tarja
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            NameFull: McCarley, Robert W.
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            NameFull: Basheer, Radhika
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              M: 01
              Text: Jan2015
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