Evidence map›Paper›PMID 28118826›Full record

ArticleRespiratory research2017

Pharmacological investigation on the anti-oxidant and anti-inflammatory activity of N-acetylcysteine in an ex vivo model of COPD exacerbation.

Mario Cazzola, Luigino Calzetta, Francesco Facciolo, Paola Rogliani, Maria Gabriella Matera

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 74 citations in OpenAlex.

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  15. Advances in the Use ofAntioxidants (Basel, Switzerland) · 2023
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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

5 authors at 2 institutions in 1 country.

Mario CazzolaDepartment of Systems Medicine, Chair of Respiratory Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133, Rome, Italy.
Luigino CalzettaDepartment of Systems Medicine, Chair of Respiratory Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133, Rome, Italy. luigino.calzetta@uniroma2.it.
Francesco FaccioloRegina Elena National Cancer Institute, Thoracic Surgery Unit, Rome, Italy.
Paola RoglianiDepartment of Systems Medicine, Chair of Respiratory Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133, Rome, Italy.
Maria Gabriella MateraDepartment of Experimental Medicine, Unit of Pharmacology, Second University of Naples, Naples, Italy.
University of Rome Tor Vergata · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOxidative stress is recognized to be one of predisposing factor in the pathogenesis of COPD. The oxidant/antioxidant imbalance is significantly pronounced in patients with COPD exacerbation. N-acetylcysteine (NAC) seems to be able to reduce COPD exacerbations by modulating the oxidative stress in addition to its well-known mucolytic activity, but there are discordant findings on the actual anti-oxidant activity of NAC.

methodsThe anti-oxidant effect of NAC and its impact on the inflammatory response have been pharmacologically characterized on a human ex vivo model of COPD exacerbation induced by lipopolysaccharide (LPS).

resultsNAC prevented the desensitization induced by LPS incubation on the contractile tone in linear concentration-response manner. Concentrations of NAC ≥1 μM reduced the pro-oxidant response (peroxidase activity, hydrogen peroxide, malondialdehyde, nitric oxide), and improved the anti-oxidant response (total anti-oxidant capacity, glutathione, superoxide dismutase) induced by LPS. Lower concentrations of NAC (<1 μM) did not modulate the bronchial oxidative imbalance. Concentrations of NAC ≥300 μM inhibited the inflammatory response (release of IL-1β, IL-8, and TNF-α) of human airways induced by the overnight stimulation with LPS, whereas lower concentrations of NAC (≥1 μM) were sufficient to reduce the release of IL-6 elicited by LPS. Both the anti-oxidant effect and the anti-inflammatory effect of NAC were inversely correlated with the release of NKA.

conclusionsThe findings of this study suggest that NAC may have a role in modulating the detrimental effect induced by LPS in course of COPD exacerbation. It may elicit both anti-oxidant and anti-inflammatory effects when administered at high concentrations.

Indexed as

AcetylcysteineAgedAirway ResistanceAnti-Inflammatory AgentsAntioxidantsDisease ProgressionFemaleHumansLungMaleOrgan Culture TechniquesOxidative StressPulmonary Disease, Chronic ObstructiveReactive Oxygen SpeciesTreatment OutcomeAcetylcysteineAnti-Inflammatory AgentsAntioxidantsReactive Oxygen SpeciesAnti-inflammatory effectAnti-oxidant effectCOPDLipopolysaccharideN-acetylcysteine

Identifiers

PMID28118826
PMCPMC5260037
OpenAlexW2580204349

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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.