Electroencephalographic slow-wave activity (SWA) is an electrophysiological signature of slow (0.5 to 4.0 Hz), synchronized, oscillatory neocortical activity. Changes in SWA have been reported in a wide range of neurodevelopmental disorders, such as Angelman syndrome, Down syndrome, fragile-X syndrome, and schizophrenia. These disorders are believed to be caused by developmental defects in brain connectivity. The causal link between cognitive impairments and SWA has not been established yet, but it is likely to be related to anatomical and functional abnormalities at the synapse level. Performance of learning tasks involving the cortical regions produces a local increase in SWA and is associated with branch-specific formation of dendritic spines after learning. Therefore, defects in the neuronal ensemble dynamics that underlie SWA could result in learning dysfunctions. Activity of neuronal nitric oxide synthase (nNOS) cells in the cerebral cortex correlates with SWA, and SWA production is disturbed in nNOS knockout mice. Based on these results, we hypothesize that nNOS neuronal circuits in the cortex are required for both normal cognitive functions and SWA production. According to our hypothesis, nNOS cells become activated during sleep in the cortical regions that have been involved in active processing of information during wakefulness. The activation of these nNOS cells leads to local nitric oxide (NO) production, which affects the pattern of neuronal activity, resulting in enhanced SWA and memory consolidation. We will test this hypothesis by measuring SWA and memory in the novel object recognition task following 1) the activation of nNOS-expressing cells in the vmPFC and 2) rescuing the nitric oxide production by nNOS-expressing cells in the ventromedial prefrontal cortex (vmPFC) in nNOS knockout mice. These studies will contribute to better understanding of the mechanisms of SWA production and memory consolidation and help to develop new treatments in a wide range of cognitive disorders.

Public Health Relevance

Research on the role of neuronal nitric oxide synthase (nNOS) cells in the cerebral cortex in the regulation of electroencephalographic slow-wave activity (SWA) and memory will contribute to better understanding of the mechanisms of SWA production and memory consolidation and help to develop new treatments in a wide range of cognitive disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS092926-01
Application #
8951701
Study Section
Special Emphasis Panel (ZRG1-IFCN-Q (55))
Program Officer
He, Janet
Project Start
2015-09-01
Project End
2017-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
1
Fiscal Year
2015
Total Cost
$193,050
Indirect Cost
$43,050
Name
Harvard Medical School
Department
Psychiatry
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Gerashchenko, Dmitry; Schmidt, Michelle A; Zielinski, Mark R et al. (2018) Sleep State Dependence of Optogenetically evoked Responses in Neuronal Nitric Oxide Synthase-positive Cells of the Cerebral Cortex. Neuroscience 379:189-201
Gerashchenko, Dmitry; Pasumarthi, Ravi K; Kilduff, Thomas S (2017) Plasticity-Related Gene Expression During Eszopiclone-Induced Sleep. Sleep 40:
Zielinski, Mark R; Gerashchenko, Dmitry (2017) Sleep-inducing effect of substance P-cholera toxin A subunit in mice. Neurosci Lett 659:44-47