Evidence map›Paper›PMID 30284226›Full record

ArticleJournal of molecular neuroscience : MN2018

Role of Cerium Oxide Nanoparticles in a Paraquat-Induced Model of Oxidative Stress: Emergence of Neuroprotective Results in the Brain.

Akram Ranjbar, Sara Soleimani Asl, Farzin Firozian, Hamid Heidary Dartoti, Saman Seyedabadi, Masoumeh Taheri Azandariani, Maziar Ganji

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Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
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

14 citing papers in PubMed, 37 citations in OpenAlex.

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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 at 1 institution in 1 country.

Akram RanjbarNeurophysiology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Sara Soleimani AslAnatomy Department, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Farzin FirozianDepartment of Pharmaceutical, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Hamid Heidary DartotiDepartment of Toxicology and Pharmacology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Saman SeyedabadiDepartment of Molecular Medicine and Genetic, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Masoumeh Taheri AzandarianiNeurophysiology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Maziar GanjiDepartment of Toxicology and Pharmacology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran. Maziar.ganji92@sbmu.ac.ir.ORCID http://orcid.org/0000-0002-7669-0322
Hamedan University of Medical Sciences · IR

Funding

Neurophysiology Research Center, Hamadan University of Medical Sciences 9410015229
6 · The paper itself

Abstract

Paraquat (PQ), as a widely used herbicide, enhances the formation of free radicals and oxidative stress. Cerium oxide nanoparticles (CeNPs) are one of the most utilized and effective nanoparticles having strong antioxidative properties and inhibiting free radicals. Here, we aimed to investigate the effects of CeNPs on brain oxidative toxic stress injury induced with PQ. The male rats were treated intraperitoneally daily with PQ (50 mg/kg/day) and CeNPs (15, 30, and 60 mg/kg/day) alone or in combination for 2 weeks. After treatments, the brain tissue samples were collected. Oxidative toxic stress biomarkers including lipid peroxidation (LPO), total antioxidant capacity (TAC), and total thiol molecules (TTM) as well as DNA damage and caspase-3 levels were measured. Moreover, the mRNA expression levels of Nestin and Neurod1 were assayed. Our results showed that PQ has significantly increased brain LPO, DNA damage, and caspase-3 levels and further reduced TAC and TTM contents, as well as expression levels of Nestin and Neurod1, compared with the control group (injection of saline). CeNPs (15- and 30-mg/kg doses) in groups co-administered with PQ significantly ameliorated the LPO, DNA damage, and caspase-3 levels while increasing TAC and TTM contents as well as enhancing Nestin and Neurod1 mRNA expression levels in the brain samples (P < 0.05). These findings suggest a neuroprotective and antioxidant role for CeNPs in PQ-induced brain injury. However, further studies are required to clarify its clinical/pharmacological significance.

Indexed as

Lipid PeroxidationAnimalsAntioxidantsBrainCeriumDNA DamageHerbicidesMaleMetal NanoparticlesNeuroprotective AgentsNeurotoxicity SyndromesParaquatRatsRats, WistarAntioxidantsceric oxideCeriumHerbicidesNeuroprotective AgentsParaquatApoptosisBrainCerium oxide nanoparticleDNA damageOxidative stressParaquat

Identifiers

PMID30284226
OpenAlexW2894850367

What OpenQuestion holds

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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.