Evidence map›Paper›PMID 39630315›Full record

ArticleJournal of molecular histology2024

Involvement of necroptosıs and apoptosıs ın protectıve effects of cyclosporın a on ischemıa-reperfusıon injury in rat kıdney.

Zeynep Erdogmus Ozgen, Meral Erdinc, Meryem Seyda Kaya, Fesih Aktar, Selver Ozsener Ozekinci, Levent Erdinc, Emre Uyar

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Article in Journal of molecular histology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Zeynep Erdogmus OzgenDepartment of Pharmacology, School of Pharmacy, Dicle University, Diyarbakir, Turkey. zeynep.erdogmus@dicle.edu.tr.
Meral ErdincDepartment of Pharmacology, School of Medicine, Dicle University, Diyarbakir, Turkey.
Meryem Seyda KayaDepartment of Pharmacology, School of Pharmacy, Dicle University, Diyarbakir, Turkey.
Fesih AktarDepartment of Pediatrics, School of Medicine, Dicle University, Diyarbakir, Turkey.
Selver Ozsener OzekinciDepartment of Pathology, School of Medicine, Dicle University, Diyarbakir, Turkey.
Levent ErdincDepartment of Biochemistry, School of Medicine, Dicle University, Diyarbakir, Turkey.
Emre UyarDepartment of Pharmacology, School of Medicine, Uskudar University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to investigate the protective effects of low dose cyclosporin A (CsA) on ischemia-reperfusion (IR) injury in rat the kidney and on the apoptotic and necroptotic mechanisms involved. 1. Control group (received a single intraperitoneal (i.p.) dose of 1 ml sterile saline 15 min before the surgical procedure), 2. IR group (was subjected to 30 min of bilateral kidney ischemia followed by 90 min of reperfusion; and received a single i.p. dose of 1 ml sterile saline 15 min before the IR procedure, 3. IR + CsA group (received a single i.p. dose of 3 mg/kg CsA 15 min before the IR procedure. Renal functions (renal perfusion pressures, and serum urea-creatinine levels), kidney histological scores, MDA levels, and TNF-α, caspase-3, RIP1, RIP3, MLKL, CaMKII and CypD protein expressions were also measured. Renal perfusion pressures (PP), serum urea and creatinine levels, renal tissue MDA levels, and the protein expression levels of TNF-α, caspase-3, RIP1, RIP3, MLKL, CAMKII and CypD were significantly increased in the IR group compared to the control group (p < 0.05), Additionally, there were significant decreases in all the parameters in the IR + CsA group compared to those in the IR group (p < 0.05). Furthermore, histopathological analyses revealed significantly higher kidney injury scores in the IR group compared to the control group, and low dose CsA treatment improved the injury. A single low dose of CsA injection 15 min before IR, demonstrated a protective effect on bilateral renal IR injury and a reduction in apoptotic and necroptopic markers which is resulted in improvement of renal functions.

Indexed as

ApoptosisCyclosporineKidneyNecroptosisReperfusion InjuryAnimalsMaleProtective AgentsRatsCyclosporineProtective AgentsCAMKIICaspase-3CypDLow dose cyclosporin A (CsA)MLKLRenal ischemia–reperfusion (IR)Renal perfusion pressureRIP1RIP3TNF-α

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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.