Evidence map›Paper›PMID 27689110›Full record

ArticleJournal of renal injury prevention2016

Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference.

Fatemeh Moslemi, Pegah Taheri, Mahdis Azimipoor, Sina Ramtin, Mostafa Hashemianfar, Ali Momeni-Ashjerdi, Fatemeh Eshraghi-Jazi, Ardeshir Talebi, Hamid Nasri, Mehdi Nematbakhsh

Open access · bronzeAbstract read
In one paragraph

Article in Journal of renal injury prevention, 2016. 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
1.1field-weighted citation impact, top 19% 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, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  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

10 authors at 1 institution in 1 country.

Fatemeh MoslemiWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Pegah TaheriWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Mahdis AzimipoorWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Sina RamtinWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Mostafa HashemianfarWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Ali Momeni-AshjerdiWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Fatemeh Eshraghi-JaziWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Ardeshir TalebiWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Hamid NasriWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Mehdi NematbakhshWater & Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran ; Department of Physiology, Isfahan University of Medical Sciences, Isfahan, Iran ; IsfahanMN Institute of Basic & Applied Sciences Research, Isfahan Iran.
Isfahan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal ischemia/reperfusion (I/R) injury may be related to activity of reninangiotensin system (RAS), which is gender-related. In this study, it was attempted to compare the effect of angiotensin II (Ang II) receptor type 1 (AT1R) blockade; losartan in I/R injury in male and female rats. MATERIALS AND

methodsMale and female Wistar rats were assigned as sham surgery, control I/R groups treated with vehicle, and case I/R groups treated with losartan (30 mg/kg). Vehicle and losartan were given 2 hours before bilateral kidney ischemia induced by clamping renal arteries for 45 minutes followed by 24 hours of renal reperfusion.

resultsThe I/R injury significantly increased the serum levels of blood urea nitrogen (BUN) and creatinine (Cr), and kidney tissue damage score in both genders. However, losartan decreased these values in female rats significantly (P < 0.05). This was not observed in male rats.

conclusionLosartan protects the kidney from I/R injury in female but not in male rats possibly because of gender-related difference of RAS.

Indexed as

Acute kidney injuryGenderIschemia reperfusion injuryLosartan

Identifiers

PMID27689110
PMCPMC5040000
OpenAlexW2516237911

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.