Evidence map›Paper›PMID 24796787›Full record

ArticlePloS one2014

Losartan improved antioxidant defense, renal function and structure of postischemic hypertensive kidney.

Milan Ivanov, Nevena Mihailović-Stanojević, Jelica Grujić Milanović, Đurđica Jovović, Jasmina Marković-Lipkovski, Sanja Ćirović, Zoran Miloradović

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 43 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

7 authors at 1 institution in 1 country.

Milan IvanovDepartment of Cardiovascular Physiology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia.
Nevena Mihailović-StanojevićDepartment of Cardiovascular Physiology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia.
Jelica Grujić MilanovićDepartment of Cardiovascular Physiology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia.
Đurđica JovovićDepartment of Cardiovascular Physiology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia.
Jasmina Marković-LipkovskiInstitute of Pathology, Medical Faculty, University of Belgrade, Belgrade, Serbia.
Sanja ĆirovićInstitute of Pathology, Medical Faculty, University of Belgrade, Belgrade, Serbia.
Zoran MiloradovićDepartment of Cardiovascular Physiology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia.
University of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic acute renal failure (ARF) is a highly complex disorder involving renal vasoconstriction, filtration failure, tubular obstruction, tubular backleak and generation of reactive oxygen species. Due to this complexity, the aim of our study was to explore effects of Angiotensin II type 1 receptor (AT1R) blockade on kidney structure and function, as well as oxidative stress in spontaneously hypertensive rats (SHR) after renal ischemia reperfusion injury. Experiments were performed on anaesthetized adult male SHR in the model of ARF with 40 minutes clamping the left renal artery. The right kidney was removed and 40 minutes renal ischemia was performed. Experimental groups received AT1R antagonist (Losartan) or vehicle (saline) in the femoral vein 5 minutes before, during and 175 minutes after the period of ischemia. Biochemical parameters were measured and kidney specimens were collected 24 h after reperfusion. ARF significantly decreased creatinine and urea clearance, increased LDL and lipid peroxidation in plasma. Treatment with losartan induced a significant increase of creatinine and urea clearance, as well as HDL. Lipid peroxidation in plasma was decreased and catalase enzyme activity in erythrocytes was increased after losartan treatment. Losartan reduced cortico-medullary necrosis and tubular dilatation in the kidney. High expression of pro-apoptotic Bax protein in the injured kidney was downregulated after losartan treatment. Our results reveal that angiotensin II (via AT1R) mediates the most postischemic injuries in hypertensive kidney through oxidative stress enhancement. Therefore, blockade of AT1R may have beneficial effects in hypertensive patients who have developed ARF.

Indexed as

Angiotensin Receptor AntagonistsAnimalsAntioxidantsbcl-2-Associated X ProteinCatalaseCholesterol, LDLCreatinineDown-RegulationKidneyKidney Function TestsLipid PeroxidationLosartanMaleOxidative StressRats, Inbred SHRReperfusion InjuryAngiotensin Receptor AntagonistsAntioxidantsBax protein, ratbcl-2-Associated X ProteinCatalaseCholesterol, LDLCreatinineLosartanUrea

Identifiers

PMID24796787
PMCPMC4010520
OpenAlexW2064052178

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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.