Evidence map›Paper›PMID 34669875›Full record

ArticleClinics (Sao Paulo, Brazil)2021

The renoprotective effects of Heme Oxygenase-1 during contrast-induced acute kidney injury in preclinical diabetic models.

Cassiane Dezoti da Fonseca, Mirian Watanabe, Sheila Marques Fernandes Couto, Alef Aragão Carneiro Dos Santos, Fernanda Teixeira Borges, Maria de Fatima Fernandes Vattimo

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 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

6 authors at 3 institutions in 1 country.

Cassiane Dezoti da FonsecaEscola Paulista de Enfermagem, Universidade Federal de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0002-2118-8562
Mirian WatanabeCentro Universitario das Faculdades Metropolitanas Unidas (FMU), Sao Paulo, SP, BR.ORCID 0000-0003-4264-3744
Sheila Marques Fernandes CoutoLaboratorio Experimental de Modelos Animais (LEMA), Escola de Enfermagem, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0003-2072-9387
Alef Aragão Carneiro Dos SantosPrograma de Pos-graduacao Interdisciplinar em Ciencias da Saude, Universidade Cruzeiro do Sul, Sao Paulo SP, BR.ORCID 0000-0002-8479-0796
Fernanda Teixeira BorgesPrograma de Pos-graduacao Interdisciplinar em Ciencias da Saude, Universidade Cruzeiro do Sul, Sao Paulo SP, BR.ORCID 0000-0002-9790-0915
Maria de Fatima Fernandes VattimoLaboratorio Experimental de Modelos Animais (LEMA), Escola de Enfermagem, Universidade de Sao Paulo, Sao Paulo, SP, BR.ORCID 0000-0002-7036-5676
Associação Paulista de Medicina · BRUniversidade Cruzeiro do Sul · BRCentro Universitário das Faculdades Metropolitanas Unidas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesContrast-induced acute kidney injury (CI-AKI) is an important clinical problem that can be aggravated by diabetes mellitus, a major risk factor. However, heme oxygenase-1 (HO-1), a promising therapeutic target, can exert antioxidant effects against CI-AKI. Thus, we investigated the role of HO-1 in CI-AKI in the presence of diabetes mellitus.

methodsTwenty-eight male Wistar rats weighing 250-300g were subjected to left uninephrectomy, and concomitantly, diabetes induced by streptozotocin (65 mg/kg). After 12 weeks, iodinated contrast (meglumine ioxithalamate, 6 mL/kg) and hemin (HO-1 inducer-10 mg/k) were administered 60 min before iodinated contrast treatment. The rats were randomly divided into four groups: control, diabetes mellitus (DM), DM iodinated contrast (DMIC), and DMIC hemin (DMICH). Kidney function, albuminuria, oxidative profile, and histology were assessed. All experimental data were subjected to statistical analyses.

resultsCI-AKI in preclinical diabetic models decreased creatinine clearance and increased urinary neutrophil gelatinase-associated lipocalin (NGAL) levels and the degree of albuminuria. Additionally, the levels of oxidative and nitrosative stress metabolites (urinary peroxides, thiobarbituric acid-reactive substances, and NO) were elevated, while thiol levels in kidney tissue were reduced. Kidney histology showed tubular cell vacuolization and edema. HO-1 inducer treatment improved kidney function and reduced urinary the NGAL levels. The oxidative profile showed an increase in the endogenous thiol-based antioxidant levels. Additionally, the tubular injury score was reduced following HO-1 treatment.

conclusionsOur findings highlight the renoprotective effects of HO-1 in CI-AKI and preclinical diabetic models. Therefore, HO-1 ameliorates kidney dysfunction, reduces oxidative stress, and prevents cell necrosis.

Indexed as

Acute Kidney InjuryDiabetes MellitusAnimalsHeme Oxygenase-1Heme Oxygenase (Decyclizing)KidneyMaleOxidative StressRatsRats, WistarStreptozocinHeme Oxygenase-1Heme Oxygenase (Decyclizing)Streptozocin

Identifiers

PMID34669875
PMCPMC8491594
OpenAlexW3203825671

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.