Evidence map›Paper›PMID 37701013›Full record

ArticleCureus2023

Oxidative Stress in Wistar Rats Under Acute Restraint Stress and Its Modulation by Antioxidants and Nitric Oxide Modulators.

Giridhari Pal, Hara Prasad Mishra, Tarun Kumar Suvvari, Anshul Tanwar, Tamoghna Ghosh, Pankaj Verma, Abhilasha Pal, Kuldeep Patial, Chinmaya Mahapatra, Nidhal A Amanullah and 3 more

Open access · diamondAbstract read
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Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 12 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

13 authors at 7 institutions in 3 countries.

Giridhari PalPharmacology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, IND.
Hara Prasad MishraClinical Trial, All India Institute of Medical Sciences, New Delhi, Delhi, IND.
Tarun Kumar SuvvariMedicine and Surgery, Squad Medicine and Research (SMR), Visakhapatnam, IND.
Anshul TanwarPharmacology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, IND.
Tamoghna GhoshMedicine, All India Institute of Medical Sciences, New Delhi, Delhi, IND.
Pankaj VermaPharmacology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, IND.
Abhilasha PalZoology, Miranda House, University of Delhi, Delhi, IND.
Kuldeep PatialSleep Medicine Division, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, IND.
Chinmaya MahapatraSchool of Pharmacy, The Neotia University, Sarisha, IND.
Nidhal A AmanullahPsychiatry and Behavioral Sciences, Sree Ramakrishna Mission Hospital, Thiruvananthapuram, IND.
Sara A ShukoorPsychiatry, Government Medical College Trivandrum, Trivandrum, IND.
Sibin KamalPain and Palliative Medicine, IQRAA International Hospital & Research Centre, Kandhla, IND.
Vishwajeet RohilBiochemistry, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, IND.
University of Delhi · INAll India Institute of Medical Sciences · INGovernment Medical College · INIndra (Spain) · ESRamakrishna Mission Vidyamandira · INRangaraya Medical College · INThe Football Association · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral pathogenic conditions leading to morbidity, including cancer, aging, diabetes, reperfusion injury, cardiovascular disease, and neurological disorders, are known to be exacerbated by oxidative stress. Antioxidant therapy is effective in the treatment of such disorders and appears to be a potential therapeutic technique to reduce oxidative stress. The aim of our study is to investigate the antioxidant effects of L-ascorbic acid and nitric oxide (NO) modulators on rats suffering from oxidative stress induced by acute restraint stress (RSx1). METHODOLOGY: In this in vivo study, Wistar rats were subjected to one hour of restraint stress on day 21 to induce oxidative stress. Superoxide dismutase (SOD), total antioxidant capacity (TAC), catalase, glutathione (GSH), and malondialdehyde (MDA) were used to assess the antioxidant effects. IBM Corp. Released 2013. IBM SPSS Statistics for Windows, Version 22.0. Armonk, NY: IBM Corp. was used for data analysis.

resultsCompared to vehicle groups, acute restraint stress (RSx1) dramatically increased MDA levels while decreasing GSH, SOD, total antioxidant capacity, and catalase. L-NAME, 7-NI, AG (50 mg/kg each), and L-ascorbic acid (200 mg/kg) reversed the changes in SOD, MDA, GSH, total antioxidant capacity, and catalase levels. The NO precursor L-arginine (1000 mg/kg) and NO synthase inhibitors followed the same trend.

conclusionOur study findings highlight the complex role of antioxidants and NO modulators in the pathogenesis of diseases, as evidenced by the reversal of oxidative stress indicators. Antioxidant therapy, with its potential to mitigate oxidative stress, emerges as a viable treatment option for a range of pathological conditions associated with oxidative stress.

Indexed as

antioxidantsin vivo studynitric oxide modulatorsrestraint stresswister rats

Identifiers

PMID37701013
PMCPMC10493075
OpenAlexW4385749306

What OpenQuestion holds

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LicenceCC BY
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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.