Evidence map›Paper›PMID 30371896›Full record

ArticleSleep2019

Sleep disruption elevates oxidative stress in parvalbumin-positive cells of the rat cerebral cortex.

John H Harkness, Priyanka N Bushana, Ryan P Todd, William C Clegern, Barbara A Sorg, Jonathan P Wisor

Abstract read
In one paragraph

Article in Sleep, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Review
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  3. Article
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  9. Review
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  11. Review
  12. Article
  13. Sleep, Narcolepsy, and Sodium Oxybate.Current neuropharmacology · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
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  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

John H HarknessDepartment of Integrative Physiology and Neuroscience, Translational Addiction Research Center, Washington State University, Vancouver, WA.
Priyanka N BushanaDepartment of Biomedical Sciences, Elson S. Floyd College of Medicine, Spokane, WA.
Ryan P ToddDepartment of Integrative Physiology and Neuroscience, Translational Addiction Research Center, Washington State University, Vancouver, WA.
William C ClegernDepartment of Biomedical Sciences, Elson S. Floyd College of Medicine, Spokane, WA.
Barbara A SorgDepartment of Integrative Physiology and Neuroscience, Translational Addiction Research Center, Washington State University, Vancouver, WA.
Jonathan P WisorDepartment of Biomedical Sciences, Elson S. Floyd College of Medicine, Spokane, WA.

Funding

Sleep deprivation elevates, and sleep alleviates, oxidative stress in the brain.R01NS078498 · NINDS · WASHINGTON STATE UNIVERSITY · PI WISOR, JONATHAN P · 2012 to 2022
$3.0M
Perineuronal nets and cocaine-associated memoriesR01DA040965 · NIDA · WASHINGTON STATE UNIVERSITY · PI BROWN, TRAVIS EUGENE, SORG, BARBARA A · 2016 to 2020
$2.0M
Extracellular Matrix, Cocaine, and MemoryR01DA033404 · NIDA · WASHINGTON STATE UNIVERSITY · PI SORG, BARBARA A · 2012 to 2016
$1.5M
NIDA NIH HHS R01 DA033404NIDA NIH HHS R01 DA040965NINDS NIH HHS R01 NS078498
6 · The paper itself

Abstract

We used a novel automated sleep disruption (SD) apparatus to determine the impact of SD on sleep and molecular markers of oxidative stress in parvalbumin (PV) neurons in the rat prefrontal cortex (PFC). Rats were subjected to two 6 hr SD sessions from zeitgeber time (ZT) 0 to ZT6, one by the gentle handling method and the other by an automated agitator running the length of the rat's home cage floor (a novel SD method). The same rats were later subjected to a 12 hr SD session from ZT0 to ZT12. Sleep was disrupted with both methods, although rats slept less during gentle handling than during the automated condition. Immediately after both SD sessions, rats displayed compensatory sleep characterized by elevated slow-wave activity. We measured in the prelimbic prefrontal cortex (prelimbic PFC; 6 and 12 hr SD) and orbital frontal cortex (12 hr SD) the intensity of the oxidative stress marker, 8-oxo-2'-deoxyguanosine (8-oxo-dG) as well as the staining intensity of PV and the PV cell-associated perineuronal net marker, Wisteria floribunda agglutinin (WFA). In the prelimbic PFC, 6 hr SD increased the intensity of 8-oxo-dG, PV, and WFA. After 12 hr SD, the intensity of 8-oxo-dG was elevated in all neurons. PV intensity was elevated only in neurons colabeled with 8-oxo-dG or WFA, and no changes were found in WFA intensity. We conclude that in association with SD-induced sleep drive, PV neurons in the prelimbic PFC exhibit oxidative stress.

Indexed as

8-Hydroxy-2'-DeoxyguanosineAnimalsAnxietyMaleNeuronsOxidative StressParvalbuminsPlant LectinsPrefrontal CortexRatsRats, Sprague-DawleyReceptors, N-AcetylglucosamineSleepSleep DeprivationWakefulness8-Hydroxy-2'-DeoxyguanosineParvalbuminsPlant LectinsReceptors, N-Acetylglucosaminewisteria lectin

Identifiers

PMID30371896
PMCPMC6335871

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.