Evidence map›Paper›PMID 36762326›Full record

ArticleJournal of medicine and life2022

Nephroprotective effects of Candesartan Cilexetil against Cyclosporine A-induced nephrotoxicity in a rat model.

Fadhaa Abdulameer Ghafil, Samah Abdulridha Abdul Kadhim, Sahar Majeed, Heider Qassam, Najah Rayish Hadi

Open access · diamondAbstract read
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Article in Journal of medicine and life, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 4 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

5 authors at 2 institutions in 1 country.

Fadhaa Abdulameer GhafilDepartment of Pharmacology and Therapeutics, Faculty of Medicine, University of Kufa, Najaf, Iraq.
Samah Abdulridha Abdul KadhimAl-Diwanyah Health Directorate, Al-Diwanyah, Iraq.
Sahar MajeedDepartment of Pharmacology and Therapeutics, Faculty of Medicine, University of Kufa, Najaf, Iraq.
Heider QassamDepartment of Pharmacology and Therapeutics, Faculty of Medicine, University of Kufa, Najaf, Iraq.
Najah Rayish HadiDepartment of Pharmacology and Therapeutics, Faculty of Medicine, University of Kufa, Najaf, Iraq.
University of Kufa · IQUniversity of Al-Qadisiyah · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclosporine A (CsA), a well-known immunosuppressive drug, has been prescribed after organ transplantation and in a variety of disorders with an immunological origin. Nephrotoxicity is one of the most frequently stated problems associated with CsA, and therefore the treatment with CsA remains a big challenge. This study sets out to assess the ameliorative influences of Candesartan Cilexetil (CC) on oxidative stress and the nephrotoxic effect of CsA in a rat model. Twenty-four Wister Albino rats, 7-8-week-old, weighing 150-250g, were randomly categorized into three groups (eight animals in each group). These groups were the (1) CsA-treated group, (2) vehicle-treated group, and (3) CC-treated group. Bodyweights were assessed at the start and end of experiments. Renal function test and levels of glutathione peroxidase 1 catalase -CAT (Gpx1), catalase (CAT), superoxide dismutase (SOD), interleukin -2 (IL-2), and malondialdehyde (MDA) were investigated in renal tissues. Histological changes in kidneys were also evaluated. Data showed that levels of urea and creatinine in serum and levels of IL-2 and MDA in renal tissues were elevated in the CsA-treated group, with severe histological changes compared with the control group. Furthermore, tissue levels of Gpx1, CAT, and SOD were significantly decreased in CsA-treated in comparison with the control group. Treatment with CC for the rats subjected to CSA resulted in a marked reduction in levels of serum urea and creatinine and tissue levels of IL-2 and MDA. Levels of Gpx1, CAT, and SOD in renal tissues were greater in the CC-treatment group compared with the CsA-treated group. CC treatment reduced the deterioration of renal morphology compared with CsA treatment. The findings of this study suggest that CC could prevent CSA-induced nephrotoxicity through its anti-inflammatory and antioxidant influences. Considerably more work needs to be done to determine the mechanistic insight behind the ameliorative effect of CC.

Indexed as

Kidney DiseasesRenal InsufficiencyAnimalsBenzimidazolesBiphenyl CompoundsCatalaseCreatinineCyclosporineImmunosuppressive AgentsInterleukin-2KidneyOxidative StressRatsRats, WistarSuperoxide DismutaseTetrazolesBenzimidazolesBiphenyl Compoundscandesartan cilexetilCatalaseCreatinineCyclosporineImmunosuppressive AgentsInterleukin-2Superoxide DismutaseTetrazolesUreaCandesartan Cilexetil (CC)CAT – catalaseCC – Candesartan CilexetilCOX2 – Cyclooxygenase-2CsA – cyclosporin ACyclosporine A (CsA)GFR – glomerular filtration rateGpx1 – glutathione peroxidase 1IL-2 – interleukin-2MDA – malondialdehydenephrotoxicityNFκB – Nuclear factor kappa BRAAS – renin-angiotensin-aldosterone systemROS – reactive oxygen speciesSOD – superoxide dismutaseTGF-ß1 – transforming growth factor beta 1VEGF – vascular endothelial growth factor

Identifiers

PMID36762326
PMCPMC9884341
OpenAlexW4319827228

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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.