Evidence map›Paper›PMID 39976720›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

Gallic acid alleviates omeprazole-induced depressive behavior and memory impairment.

Noreen Samad, Natasha Manzoor, Ali Irfan, Arslan Khalid, Umer Ejaz, Bakar Bin Khatab Abbas, Syed Aun Muhammad, Gamal A Shazly, Saima Khaliq, Yousef A Bin Jardan

Abstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. 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.

Noreen SamadDepartment of Biochemistry, Faculty of Science, Bahauddin Zakariya University, Multan, 60800, Pakistan. noreen.samad@bzu.edu.pk.
Natasha ManzoorDepartment of Biochemistry, Faculty of Science, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Ali IrfanDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan. raialiirfan@gmail.com.
Arslan KhalidDepartment of Biochemistry, Faculty of Science, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Umer EjazDepartment of Biochemistry, Faculty of Science, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Bakar Bin Khatab AbbasDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA, 02115, USA.
Syed Aun MuhammadInstitute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Gamal A ShazlyDepartment of Pharmaceutics, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia.
Saima KhaliqDepartment of Biochemistry, Federal Urdu University of Science and Technology, Karachi, Pakistan.
Yousef A Bin JardanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia. ybinjardan@ksu.edu.sa.

Funding

King Saud University RSP2024R457
6 · The paper itself

Abstract

The study aims to evaluate the effect of various doses of gallic acid (GA) on omeprazole (OMZ)-induced depression, memory impairment, oxido-neuroinflammation, and altered serotonergic neurotransmission in the midbrain and cerebral cortex of rats. Forty-eight male rats were divided into six groups (n = 8): Veh (vehicle), Veh + GA (50 mg/kg/ml), Veh + GA (100 mg/kg/ml), OMZ (20 mg/kg/ml), OMZ + GA (50 mg/kg/ml), and OMZ + GA (100 mg/kg/ml). Animals received their respective treatment intraperitoneally, daily for 4 weeks. After that, behavioral analysis for depression and memory function was performed; then, animals were decapitated, and their brains were removed from skulls. Brain regions, i.e., midbrain and cerebral cortex, were isolated for various biochemical and neurochemical studies. Results showed that OMZ-induced depression-like behavior and memory impairment were attenuated by GA in a dose-dependent manner. OMZ instigated decreased antioxidant enzyme activity and serotonergic mechanism, and increased oxido-neuroinflammation and acetylcholinesterase (AChE) activity were normalized by dose-dependent GA administration in both regions. In silico study also showed that GA has a potent antioxidant effect on the brain. In conclusion, the present findings revealed that GA, as a potential agent that reduced PPIs, induced depression-like behavior and memory impairment. The supplementation of GA as a dietary constituent could provide relief against OMZ-induced negative effects.

Indexed as

Antidepressive AgentsBehavior, AnimalDepressionGallic AcidMemory DisordersOmeprazoleAcetylcholinesteraseAnimalsAntioxidantsCerebral CortexDisease Models, AnimalDose-Response Relationship, DrugMaleMaze LearningMemoryRatsAcetylcholinesteraseAntidepressive AgentsAntioxidantsGallic AcidOmeprazoleDepressionGallic acidMemoryNeuromodulationOmeprazole

Identifiers

PMID39976720
PMCPMC12350505

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.