Evidence map›Paper›PMID 39015099›Full record

ArticleCNS neuroscience & therapeutics2024

Propofol improves sleep deprivation-induced sleep structural and cognitive deficits via upregulating the BMAL1 expression and suppressing microglial M1 polarization.

Huan Liu, Chenyi Yang, Xiaoqing Wang, Baochen Yu, Ying Han, Xinyi Wang, Zixuan Wang, Miao Zhang, Haiyun Wang

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. Cognitive and Motor Dysfunction in STXBP1 R406H Mice.Journal of molecular neuroscience : MN · 2026
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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

9 authors.

Huan LiuThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.ORCID 0009-0000-1797-1039
Chenyi YangNankai University, Tianjin, China.ORCID 0000-0002-7299-3668
Xiaoqing WangThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.
Baochen YuThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.
Ying HanNankai University Affinity the Third Central Hospital, Tianjin, China.
Xinyi WangNankai University Affinity the Third Central Hospital, Tianjin, China.
Zixuan WangThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.
Miao ZhangThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.
Haiyun WangThe Third Central Clinical College of Tianjin Medical University, Tianjin, China.ORCID 0000-0002-0084-2342

Funding

National Natural Science Foundation of China 82071220National Natural Science Foundation of China 82371205Tianjin Health Research Project TJWJ2023XK019Tianjin key Medical Discipline (Specialty) Construction Project TJYXZDXK-072CTianjin Multiple Investment Foundation of Applied Basic Research 21JCQNJC01020
6 · The paper itself

Abstract

backgroundSleep deprivation (SD) is a growing global health problem with many deleterious effects, such as cognitive impairment. Microglia activation-induced neuroinflammation may be an essential factor in this. Propofol has been shown to clear sleep debt after SD in rats. This study aims to evaluate the effects of propofol-induced sleep on ameliorating sleep quality impairment and cognitive decline after 48 h SD.

methodsAlmost 8-12-week-old rats were placed in the SD system for 48 h of natural sleep or continuous SD. Afterwards, rats received propofol (20 mg·kg

resultsCompared to the control group, the sleep-deprived rats showed poor cognitive performance on both the MWM test and the Y-maze test, accompanied by disturbances in sleep structure, including increased total sleep time, and increased time spent and delta power in non-rapid eye movement sleep. In addition, SD induces abnormal expression of the circadian rhythm protein BMAL1, activates microglia, and causes neuroinflammation and nerve damage. Propofol reversed these changes and saved sleep and cognitive impairment. Furthermore, propofol treatment significantly reduced hippocampal IL-1β and IL-6 levels, increased BDNF, Arg1, and IL-10 levels, and switched microglia surface markers from the inflammatory M1 type to the anti-inflammatory M2 type.

conclusionPropofol reduces SD-induced cognitive impairment and circadian rhythm disruption, possibly by lowering neuronal inflammation and switching the microglia phenotype from an M1 to an M2 activated state, thus exerting neuroprotective effects.

Indexed as

ARNTL Transcription FactorsCognitive DysfunctionMaze LearningMicrogliaPropofolRats, Sprague-DawleySleep DeprivationAnimalsBrain-Derived Neurotrophic FactorHippocampusMaleRatsSleepUp-RegulationArntl protein, ratARNTL Transcription FactorsBrain-Derived Neurotrophic FactorPropofolcognitive impairmentmicrogliapropofolsleepsleep deprivation

Identifiers

PMID39015099
PMCPMC11252557

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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.