Evidence map›Paper›PMID 33639837›Full record

ArticleBMC neuroscience2021

Homeostatic sleep regulation in the absence of the circadian sleep-regulating component: effect of short light-dark cycles on sleep-wake stages and slow waves.

Örs Szalontai, Attila Tóth, Máté Pethő, Dóra Keserű, Tünde Hajnik, László Détári

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 41% of its field
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

3 citing papers in PubMed, 8 citations in OpenAlex.

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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 at 1 institution in 1 country.

Örs SzalontaiIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary.
Attila TóthIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary.
Máté PethőIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary.
Dóra KeserűIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary.
Tünde HajnikIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary.
László DétáriIn vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Institute of Biology, Department of Physiology and Neurobiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, 1117, Budapest, Hungary. laszlo.detari@ttk.elte.hu.ORCID 0000-0002-0630-8466
Eötvös Loránd University · HU

Funding

VEKOP VEKOP-2.3.3-15-2017-00019
6 · The paper itself

Abstract

backgroundAside from the homeostatic and circadian components, light has itself an important, direct as well as indirect role in sleep regulation. Light exerts indirect sleep effect by modulating the circadian rhythms. Exposure to short light-dark cycle (LD 1:1, 1:1 h light - dark) eliminates the circadian sleep regulatory component but direct sleep effect of light could prevail. The aim of the present study was to examine the interaction between the light and the homeostatic influences regarding sleep regulation in a rat model.

methodsSpontaneous sleep-wake and homeostatic sleep regulation by sleep deprivation (SD) and analysis of slow waves (SW) were examined in Wistar rats exposed to LD1:1 condition using LD12:12 regime as control.

resultsSlow wave sleep (SWS) and REM sleep were both enhanced, while wakefulness (W) was attenuated in LD1:1. SWS recovery after 6-h total SD was more intense in LD1:1 compared to LD12:12 and SWS compensation was augmented in the bright hours. Delta power increment during recovery was caused by the increase of SW number in both cases. More SW was seen during baseline in the second half of the day in LD1:1 and after SD compared to the LD12:12. Increase of SW number was greater in the bright hours compared to the dark ones after SD in LD1:1. Lights ON evoked immediate increase in W and decrease in both SWS and REM sleep during baseline LD1:1 condition, while these changes ceased after SD. Moreover, the initial decrease seen in SWS after lights ON, turned to an increase in the next 6-min bin and this increase was stronger after SD. These alterations were caused by the change of the epoch number in W, but not in case of SWS or REM sleep. Lights OFF did not alter sleep-wake times immediately, except W, which was increased by lights OFF after SD.

conclusionsPresent results show the complex interaction between light and homeostatic sleep regulation in the absence of the circadian component and indicate the decoupling of SW from the homeostatic sleep drive in LD1:1 lighting condition.

Indexed as

PhotoperiodAnimalsBrainCircadian RhythmElectrocorticographyHomeostasisMaleRatsRats, WistarSleep StagesWakefulnessCircadian sleep regulationHomeostatic sleep regulationShort light-dark cyclesSleep effect of lightSlow waves

Identifiers

PMID33639837
PMCPMC7913432
OpenAlexW3134125543

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.