Evidence map›Paper›PMID 40327305›Full record

ArticleMolecular neurobiology2025

Evaluation of the Protective Effects of Noscapine on Paraquat-Induced Parkinson's Disease in Rats.

Fatemeh Bosak, Vafa Baradaran Rahimi, Bashir Sobhani, Mohammad Mahdi Dabbaghi, Mohammad Soukhtanloo, Farnaz Zahedi Avval, Vahid Reza Askari

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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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. PeripheralParkinson's disease · 2026
    Article
  5. Review
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

7 authors.

Fatemeh BosakDepartment of Clinical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Vafa Baradaran RahimiDepartment of Cardiovascular Diseases, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Bashir SobhaniDepartment of Basic Sciences, Ferdowsi University of Mashhad, Mashhad, Iran.
Mohammad Mahdi DabbaghiClinical Research Development Unit, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammad SoukhtanlooDepartment of Clinical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Farnaz Zahedi AvvalDepartment of Clinical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. zahediaf@mums.ac.ir.
Vahid Reza AskariClinical Research Development Unit, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. askariv@mums.ac.ir.

Funding

Mashhad University of Medical Sciences 4001864
6 · The paper itself

Abstract

Parkinson's disease (PD) is a degenerative central nervous system disease pathologically attributed to dopaminergic neuron damage in the substantia nigra. Noscapine is a natural alkaloid with several benefits, including anti-inflammatory, neural protection, and anti-oxidant effects. Hence, the current study evaluated the protective effects of Noscapine against paraquat (PQ)-induced Parkinson's disease model in rats. Male Wistar rats were into six groups: sham and PQ-induced models treated with vehicle, vitamin-E (20 mg/kg/d), or Noscapine (6, 18, and 55 mg/kg/d) for four weeks. Meanwhile, the rats were assessed for weight and food consumption (FC) daily and PD-associated behavior changes using rotarod, bar, and parallel bar tests every week. The animals were ethically sacrificed at the end of the study, and biochemical, immunological, and histopathological markers were measured in the brain. As a result, the levels of weight, FC, parallel bar, and rotarod test (both speed and latency), number of neurons, total thiol content, and interleukin-10 (IL-10) were significantly reduced. In contrast, the levels of dark neurons, TNF-α, bar test, and malondialdehyde (MDA) were markedly increased in the PQ-vehicle group compared to the sham group (P < 0.001-0.5). In contrast, comedication with Noscapine significantly reversed the histological damages and improved deteriorated behavioral, biochemical, and immunological parameters in a dose-dependent manner compared to the PQ-vehicle group (0.001-0.05). Taken together, it was determined that using Noscapine has antiparkinsonian effects and improved behavioral tests, catalepsy, bradykinesia, and motor dysfunction and has a protective impact on the brain's neurons through its anti-oxidant and anti-inflammatory properties.

Indexed as

Neuroprotective AgentsNoscapineParaquatParkinson DiseaseAnimalsAntioxidantsBehavior, AnimalMaleOxidative StressRatsRats, WistarAntioxidantsNeuroprotective AgentsNoscapineParaquatIL-10; TNF-αInflammationOxidative stressParaquatParkinson's disease

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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.