Evidence map›Paper›PMID 41527489›Full record

ArticleBrain and behavior2026

L-Quebrachitol Enhances Sedative Effect of Diazepam Through GABAergic Pathway: Animal and Computational Studies.

Asifa Asrafi, Mohammad Aslam, Md Sakib Al Hasan, Mohammed Burhan Uddin, Emon Mia, Mohammad Y Alshahrani, Sumaya Akter Bithi, Mst Sumaia Akter, Md Arif Hossain, Md Torequl Islam

Abstract read
In one paragraph

Article in Brain and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Asifa AsrafiDepartment of Biochemistry and Molecular Biology, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Mohammad AslamDepartment of Biochemistry and Molecular Biology, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Md Sakib Al HasanDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Mohammed Burhan UddinDepartment of Chemistry, York College, City, University of New York, Jamaica, New York, USA.
Emon MiaDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Mohammad Y AlshahraniCentral Labs, King Khalid University, Abha, Saudi Arabia.
Sumaya Akter BithiDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Mst Sumaia AkterDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Md Arif HossainDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Md Torequl IslamDepartment of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.

Funding

King Khalid UniversityUniversity Higher Education CL/CO/A/8
6 · The paper itself

Abstract

introductionInsomnia and other sleep disorders are becoming increasingly prevalent worldwide, while current sedative medications such as benzodiazepines, though effective, are often limited by side effects and dependency risks. Therefore, identifying safe natural compounds with sedative potential is of growing scientific and clinical interest. L-quebrachitol (LQL), a naturally occurring cyclitol compound with antioxidant, antimicrobial, and antidiabetic properties, has not been previously evaluated for its sedative effects. The aim of this study is to evaluate the potential sedative effects of LQL through both in vivo and in silico methods.

methodsIn this experiment, 2-day-old broiler chicks (Gallus gallus domesticus) were given thiopental sodium (10 mg/kg, intraperitoneal [ip]) to induce sleep. LQL (1, 5, and 10 mg/kg, ip) and diazepam (2 mg/kg, ip) were administered alone or together to assess their synergistic or antagonistic effects on chicks. To assess its potential for interacting with the GABA

resultAccording to the in vivo investigation, the results indicate that LQL decreased the latency period while extending the animal's sleep duration time in a dose-dependent manner. Moreover, the combination of LQL-10 (10 mg/kg) and diazepam 2 (2 mg/kg) showed (p < 0.05) enhanced sedative effects significantly by decreasing latency time and prolonging sleeping duration. In addition, LQL has a moderate binding affinity of -5.3 kcal/mol against the GABA

conclusionThese findings collectively enhance the potential of LQL as an effective sedative therapeutic agent. However, further research, including in vitro studies to confirm the molecular interactions and membrane permeability, followed by well-designed clinical trials, is necessary to fully establish LQL as a safe and effective sedative agent.

Indexed as

DiazepamHypnotics and SedativesReceptors, GABA-ASleepSugar AlcoholsAnimalsChickensDrug SynergismMaleMolecular Docking SimulationDiazepamHypnotics and SedativesReceptors, GABA-ASugar Alcoholsanimal studyGABAA receptorin silico studiesL‐quebrachitolsedative effect

Identifiers

PMID41527489
PMCPMC12796828

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.