Evidence map›Paper›PMID 30610249›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2019

All-trans retinoic acid prevents cisplatin-induced nephrotoxicity in rats.

Cem Yucel, Elcin Erdogan Yucel, Fatma Demet Arslan, Sumeyye Ekmekci, Erdem Kisa, Volkan Ulker, Murat Ucar, Yusuf Ozlem Ilbey, Orcun Celik, Banu Isbilen Basok and 1 more

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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Protective effects of vitamin DPharmaceutical biology · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Disparate roles of retinoid acid signaling molecules in kidney disease.American journal of physiology. Renal physiology · 2021
    Review
  7. The yin and yang of retinoic acid signaling in kidney diseases.The Journal of clinical investigation · 2020
    Article
  8. 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

11 authors at 1 institution in 1 country.

Cem YucelDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey. meclecuy@hotmail.com.ORCID http://orcid.org/0000-0003-0838-9199
Elcin Erdogan YucelDepartment of Internal Medicine, Tepecik Training and Research Hospital, İzmir, Turkey.
Fatma Demet ArslanDepartment of Medical Biochemistry, Tepecik Training and Research Hospital, İzmir, Turkey.
Sumeyye EkmekciDepartment of Pathology, Tepecik Training and Research Hospital, İzmir, Turkey.
Erdem KisaDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Volkan UlkerDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Murat UcarDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Yusuf Ozlem IlbeyDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Orcun CelikDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Banu Isbilen BasokDepartment of Medical Biochemistry, Tepecik Training and Research Hospital, İzmir, Turkey.
Zafer KozaciogluDepartment of Urology, Tepecik Training and Research Hospital, Yenişehir Mah, Gaziler Cad. No:468, Konak, 35100, İzmir, Turkey.
Yenişehir Hospital · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study is to investigate the effects of all-trans retinoic acid (ATRA) use on cisplatin (CP)-induced nephrotoxicty. Twenty-eight rats were randomly divided into four groups. The rats in the control group were injected a single dose of 1 ml/kg saline intra-peritoneally (IP) during 10 days. The rats in the ATRA group were injected a single dose of ATRA during 10 days. The rats in the ATRA+CP group were injected a single dose of CP on the fourth day of the 10 days of ATRA treatment. The rats in the CP group were injected a single dose of CP on the fourth day of 10 days without administering a treatment. After treatment, the groups were compared with regard to total antioxidant status (TAS), total oxidant status (TOS), and oxidative stress index (OSI) levels in renal tissue and renal histopathology. The serum creatinine and urea values were statistically significantly higher in the CP group compared to the other groups. The serum creatinine and urea values were statistically significantly lower in the ATRA+CP group when compared to the CP group. Although the TOS and OSI levels were found to be lower in the ATRA+CP group compared to the CP group, the difference was not statistically significant. Administration of ATRA together with CP was observed to reduce the histopathologic destruction in the kidney and lead to mild tubular degeneration, vacuolization, and necrosis (57.1% grade 1; 28.6% grade2, and 14.3% grade 3 necrosis). The results of the present study have revealed that ATRA administration ameliorates CP-induced nephrotoxicity; however, further studies are required to identify this issue before clinical application.

Indexed as

AnimalsAntineoplastic AgentsCisplatinKidneyKidney DiseasesProtective AgentsRats, WistarTretinoinAntineoplastic AgentsCisplatinProtective AgentsTretinoinAll-trans retinoic acidCisplatinNephrotoxicity

Identifiers

PMID30610249
OpenAlexW2907346386

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.