Evidence map›Paper›PMID 42704577›Full record

ArticleDaru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences2026

Early-life GABA-A receptor blockade with bicuculline attenuates anxiety-like behaviors and cognitive deficits induced by 24-hr sleep deprivation in adult male rats.

Maryam Roushani, Fatemeh Aghaei, Zahra Mashhadi, Mohammad Amani, Hakimeh Saadati

Abstract read
In one paragraph

Article in Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maryam Roushani *Ardabil University of Medical Sciences, Ardabil, Iran.
Fatemeh Aghaei *Ardabil University of Medical Sciences, Ardabil, Iran.
Zahra Mashhadi *Ardabil University of Medical Sciences, Ardabil, Iran.
Mohammad AmaniDepartment of Physiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Hakimeh SaadatiPharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran. hsadat54@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly postnatal GABAergic signaling is crucial for brain development and circuit formation. While Gamma-aminobutyric acid (GABA) regulates sleep-wake cycles, sleep deprivation causes cognitive impairment and oxidative stress. Although blocking GABA-A receptors has been shown to improve cognition, the effect of such blockade during development on sleep-loss-induced cognitive deficits remains unknown.

objectivesAccordingly, this study was designed to investigate the effects of early-life inhibition of GABA-A receptors on sleep deprivation-induced cognitive impairments in adulthood.

methodsThirty-two male neonatal rats were randomly assigned to four equal-sized groups (n = 8/group): Control, Bicuculline (300 µg/kg subcutaneously on postnatal days 7, 9, and 11), Sleep Deprivation (24-h SD at postnatal days (PNDs) 60-70), and Bicuculline + SD. In young adulthood (PNDs 60-70), anxiety-like behavior was assessed using the Elevated plus maze (EPM), while the Morris water maze (MWM) was used to evaluate spatial learning and memory. We then measured superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities, as well as malondialdehyde (MDA) levels in hippocampal tissue.

resultsSD alone significantly increased anxiety-like behaviors, impaired spatial learning and short-term memory, reduced hippocampal SOD and GPx activities, and elevated MDA. Remarkably, early-life bicuculline pretreatment prevented SD-induced cognitive deficits, attenuated anxiety-like responses, and restored antioxidant enzyme activities while normalizing MDA levels.

conclusionEarly postnatal transient blockade of GABA-A receptors was associated with decreased vulnerability to cognitive deficits, anxiety-like behaviors, and oxidative stress induced by acute sleep deprivation in adulthood. This reveals a novel developmental role of early GABAergic signaling in defense against sleep loss-induced neuropsychiatric and cognitive deficits.

Indexed as

AnxietyBicucullineCognitive DysfunctionGABA-A Receptor AntagonistsReceptors, GABA-ASleep DeprivationAnimalsHippocampusMaleMaze LearningOxidative StressRatsRats, WistarSuperoxide DismutaseBicucullineGABA-A Receptor AntagonistsReceptors, GABA-ASuperoxide DismutaseBicucullineCognitive functionsGABA receptorHippocampusSleep deprivation

Identifiers

PMID42704577
PMCPMC13550353

What Socratic 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 Socratic graph.