Evidence map›Paper›PMID 26941804›Full record

ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2015

Biochemical and molecular evidences on the protection by magnesium oxide nanoparticles of chlorpyrifos-induced apoptosis in human lymphocytes.

Vida Heydary, Mona Navaei-Nigjeh, Mahban Rahimifard, Azadeh Mohammadirad, Maryam Baeeri, Mohammad Abdollahi

Open access · goldAbstract read
In one paragraph

Article in Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 20 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

6 authors at 1 institution in 1 country.

Vida HeydaryToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran; Islamic Azad University, Ahar Branch, Ahar, Iran.
Mona Navaei-NigjehToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran; Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran, Iran.
Mahban RahimifardToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran.
Azadeh MohammadiradToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran.
Maryam BaeeriToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran.
Mohammad AbdollahiToxicology and Poisoning Research Center, Ahar Branch, Ahar, Iran; Pharmaceutical Sciences Research Center, Ahar Branch, Ahar, Iran; Islamic Azad University, Ahar Branch, Ahar, Iran; Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran, Iran; Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Islamic Azad University of Ahar · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChlorpyrifos (CP) is one of the most widely used organophosphate (OP) insecticides in agricultural and residential pest control with its attendant adverse health effect. In the present study, it is proposed to investigate the possible modulatory role of magnesium oxide nanoparticles (MgO NPs) against CP-induced toxicity in human lymphocytes and determine the mechanisms lying behind this protection by viability and biochemical assays. MATERIALS AND

methodsIsolated lymphocytes were exposed to 12 μg/mL CP either alone or in combination with different concentrations of MgO NPs (0.1 μg/mL, 1 μg/mL, 10 μg/mL, and 100 μg/mL). After a 3-day incubation, the viability and oxidative stress markers including cellular mitochondrial activity, caspase-3 and -9 activities, total antioxidant power, lipid peroxidation, and myeloperoxidase (MPO) activity were measured. Also, the levels of tumor necrosis factor-α (TNF-α) as inflammatory index, along with acetylcholinesterase (AChE) activity were measured. Statistical differences were determined using one-way analysis of variance (ANOVA) and Dunnett's multiple comparison tests.

resultsIt is indicated that CP-exposed lymphocytes treated with MgO NPs resulted in a substantial reduction in the pace of mortality as well as the stages of oxidative stress in a dose-dependent manner. Also, MgO NPs (100 μg/mL) meaningfully restored CP-induced increase of TNF-α (P < 0.001) and decrease of AChE activity (P < 0.001) and were capable of preventing CP-treated human lymphocytes from apoptosis (P < 0.001).

conclusionOur results demonstrate that MgO NPs in approximate 100 nm diameter not only make cells resistant to the toxic properties of CP but also attenuate toxic effects of CP, which is demonstrating the potential of MgO NPs to be applied in future immune deficiency therapeutic strategies.

Indexed as

Acetylcholinesterase (AChE)antiapoptoticantioxidantchlorpyrifos (CP)human lymphocytesmagnesium oxide nanoparticle (MgO NP)organophosphate (OP)oxidative stress

Identifiers

PMID26941804
PMCPMC4755087
OpenAlexW2282568238

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.