Evidence map›Paper›PMID 41283968›Full record

ArticleMolecular neurobiology2025

Ambroxol's Role in PTZ-Induced Anxiety-Like Conditions in Mice: Targeting Neuroinflammation and Oxidative Stress via In Vivo and In Silico Approaches.

Hafeeza Zafar Ali, Sarwat Jahan, Laila Ilahi, Sami Siraj, Muhammad Zakria, Najeeb Ullah, Muhammad Ikram, Ashraf Ullah Khan, Manzoor Khan, Fawad Ali Shah and 1 more

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Article in Molecular neurobiology, 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

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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

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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

11 authors.

Hafeeza Zafar AliInstitute of Pharmaceutical Sciences, Khyber Medical University, Peshawar, Pakistan.
Sarwat JahanInstitute of Pharmaceutical Sciences, Khyber Medical University, Peshawar, Pakistan.
Laila IlahiInstitute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan.
Sami SirajInstitute of Pharmaceutical Sciences, Khyber Medical University, Peshawar, Pakistan.
Muhammad ZakriaInstitute of Pharmaceutical Sciences, Khyber Medical University, Peshawar, Pakistan.
Najeeb UllahInstitute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan.
Muhammad IkramInstitute of Pharmaceutical Sciences, Khyber Medical University, Peshawar, Pakistan. qazafi417@gmail.com.
Ashraf Ullah KhanDepartment of Pharmacy, City University of Science and information Technology, Peshawar, Pakistan.
Manzoor KhanDepartment of Clinical Research, South Oklahoma Heart Research, Oklahoma City, USA.
Fawad Ali ShahDepartment of Pharmacology, College of Pharmacy, Prince Sattam bin Abdulaziz University, Al Kharj, Saudi Arabia.
Hafsah MuhammadInstitute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anxiety disorders are major neuropsychiatric conditions linked to oxidative stress, neuroinflammation, and dysregulated neurotransmission. Current pharmacotherapies, such as benzodiazepines, offer symptomatic relief but are limited by tolerance and sedation. Ambroxol, a clinically established mucolytic agent, has demonstrated neuroprotective, anti-inflammatory, and antioxidant activities, suggesting potential therapeutic repurposing for neuropsychiatric disorders. The present study evaluated the anxiolytic and neuroprotective effects of ambroxol in a pentylenetetrazol (PTZ)-induced anxiety model in mice, supported by molecular docking and molecular dynamics analyses, showing moderate but significant interactions. Mice received ambroxol (60 mg/kg, p.o.) for 21 days, while diazepam (2 mg/kg, i.p.) served as the reference control for 14 days. Behavioral assessments were performed using the elevated plus maze, open field, light-dark box, and hole board tests. Biochemical analysis of prefrontal cortical tissue was conducted to evaluate oxidative stress and pro-inflammatory markers (MDA, SOD, CAT, GSH, TNF-α, IL-1β, NF-κB). Ambroxol significantly improved exploratory and anxiety-related behaviors, restored antioxidant enzyme activities, and suppressed cytokine levels in the prefrontal cortex. Docking and simulation studies revealed stable, biologically relevant interactions of ambroxol with TNF-α, IL-1β, and NF-κB, suggesting modulation of neuroimmune signaling. Ambroxol exhibited anxiolytic efficacy comparable to diazepam, with no apparent sedative effects observed behaviorally, although direct assessment of sedation (e.g., rotarod test) was not performed. Ambroxol demonstrated promising multi-target neuroprotective potential by concurrently attenuating oxidative and inflammatory cascades, supporting its further exploration as a safe, repurposed therapeutic candidate for anxiety disorders.

Indexed as

AmbroxolAnxietyComputer SimulationNeuroinflammatory DiseasesOxidative StressAnimalsAnti-Anxiety AgentsAntioxidantsBehavior, AnimalCytokinesDiazepamDisease Models, AnimalMaleMiceMolecular Docking SimulationPentylenetetrazoleAmbroxolAnti-Anxiety AgentsAntioxidantsCytokinesDiazepamPentylenetetrazoleAmbroxolAnxietyMolecular docking simulationsNeuroinflammationOxidative stressPentylenetetrazolSeizure

Identifiers

PMID41283968

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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.