Evidence map›Paper›PMID 41321661›Full record

ArticleCurrent research in physiology2025

Exploration of neural mechanisms underlying antidepressant-like property of

Saeedeh Ghaffarzadeh Shirabad, Samad Alimohammadi

Abstract read
In one paragraph

Article in Current research in physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Saeedeh Ghaffarzadeh ShirabadDepartment of Basic Sciences, Faculty of Veterinary Medicine, Razi University, Kermanshah, Iran.
Samad AlimohammadiDepartment of Basic Sciences, Faculty of Veterinary Medicine, Razi University, Kermanshah, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Methods: The chemical profile of EOZC obtained by GC-MS. The mice received EOZC (10, 20, and 40 mg/kg) 1 h before the FST intraperitoneally. Moreover, naloxone (non-selective antagonist for opioid receptor subtypes, 1 mg/kg), prazosin (α Results: The GC-MS evaluation demonstrated that predominant components of EOZC comprised carvacrol (65.22 %), thymol (19.51 %), p-cymene (4.86 %), γ-terpinene (4.63 %) and E-Caryophyllene (1.07 %). EOZC exhibited a significant dose-dependent effect that resulted in a marked decrease in the duration of immobility time (P < 0.05). The antidepressant-like action of EOZC was reversed by prazosin, yohimbine, WAY100635, ondansetron, haloperidol, SCH23390 and sulpiride. However, this effect remained unaffected by naloxone, propranolol and flumazenil. Conclusion: These findings indicate that EOZC elicits antidepressant-like response, which relies on its interaction with noradrenergic, serotonergic and dopaminergic pathways.

Indexed as

AntidepressantDopaminergicForced swimming testNoradrenergicSerotonergicZiziphora clinopodioides

Identifiers

PMID41321661
PMCPMC12664596

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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.