Evidence map›Paper›PMID 30012025›Full record

ArticleRenal failure2018

Acute renal involvement in organophosphate poisoning: histological and immunochemical investigations.

Yasemin Kaya, Orhan Bas, Hatice Hanci, Soner Cankaya, Ismail Nalbant, Ersan Odaci, Hüseyin Avni Uydu, Ali Aslan

Open access · goldAbstract read
In one paragraph

Article in Renal failure, 2018. 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
2.7field-weighted citation impact, top 9% 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, 22 citations in OpenAlex.

  1. Article
  2. Molecular Mechanisms of Acute Organophosphate Nephrotoxicity.International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Nephrotoxic Effects of Paraoxon in Three Rat Models of Acute Intoxication.International journal of molecular sciences · 2021
    Article
  6. Review
  7. Immunotoxic role of organophosphates: An unseen risk escalating SARS-CoV-2 pathogenicity.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Review
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

8 authors at 3 institutions in 1 country.

Yasemin Kayaa Department of Internal Medicine, Faculty of Medicine , Ordu University , Ordu , Turkey.
Orhan Basb Department of Anatomy, Faculty of Medicine , Ordu University , Ordu , Turkey.
Hatice Hancic Department of Histology and Embryology, Faculty of Medicine , Karadeniz Technical University , Trabzon , Turkey.
Soner Cankayad Department of Biostatistics, Faculty of Medicine , Ordu University , Ordu , Turkey.
Ismail Nalbante Department of Urology, Faculty of Medicine , Ordu University , Ordu , Turkey.
Ersan Odacif Department of Histology and Embryology, Faculty of Medicine , Karadeniz Technical University , Trabzon , Turkey.
Hüseyin Avni Uydug Department of Medical Biochemistry, Faculty of Medicine , Recep Tayyip Erdogan University , Rize , Turkey.
Ali Aslanh Department of Physiology, Faculty of Medicine , Ordu University , Ordu , Turkey.
Ordu University · TRKaradeniz Technical University · TRRecep Tayyip Erdoğan University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeToday, the long-term effects of partial exposure of cholinesterase on the kidney continue to be a research topic. In this study, we aimed to histopathologically investigate the possible effect of acute toxicity due to fenthion, an organophosphate (OP) compound, on the kidneys.

methodsIn all, 21 rats were randomly divided into three groups. Experimental group was each administered intraperitoneal 0.8 g/kg fenthion within physiologic serum. Sham group was only administered intraperitoneal physiologic serum. The control group continued normal nutrition with no procedure performed. After 24 h, all rats were sacrificed by cervical dislocation. Half of the recipient kidney tissues were examined histopathologically and the other half biochemically.

resultsNo histopathological findings were found in the control group. Rats in the experimental group were observed to have epithelial cell disorganization in tubules, moderate epithelial cell loss, and degeneration. Again, expansion of tubules, vacuolization of tubular epithelial cells, and tubular structure approaching atrophy were observed, with cells approaching apoptosis and common hemorrhage noted although rats in the sham group were observed to have mild tubular degeneration.

conclusionsIt should not be forgotten that one of the causes of systemic complaints linked to acute toxicity exposed to the OP compound of fenthion may be cellular injury to glomerular and tubular structures in the kidneys.

Indexed as

Acute Kidney InjuryAnimalsCholinesterase InhibitorsDisease Models, AnimalFemaleFenthionHumansKidney TubulesOrganophosphate PoisoningRatsRats, WistarCholinesterase InhibitorsFenthionfenthionhistopathological investigationOrganophosphatepoisoningrenal injury

Identifiers

PMID30012025
PMCPMC6052427
OpenAlexW2883363394

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.