Evidence map›Paper›PMID 23456824›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2013

Losartan affects glomerular AKT and mTOR phosphorylation in an experimental model of type 1 diabetic nephropathy.

Vasiliki Mavroeidi, Ioannis Petrakis, Kostas Stylianou, Theodora Katsarou, Konstantinos Giannakakis, Kostas Perakis, Eleftheria Vardaki, Spyridon Stratigis, Emmanuel Ganotakis, Stathis Papavasiliou and 1 more

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In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 26 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

11 authors at 2 institutions in 2 countries.

Vasiliki MavroeidiDepartment of Nephrology, University of Crete, Greece. vasiliki.mavroeidi@gmail.com
Ioannis Petrakis
Kostas Stylianou
Theodora Katsarou
Konstantinos Giannakakis
Kostas Perakis
Eleftheria Vardaki
Spyridon Stratigis
Emmanuel Ganotakis
Stathis Papavasiliou
Eugenios Daphnis
University of Crete · GRSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The AKT-mTOR pathway is activated in diabetic nephropathy. Renin-angiotensin system modulators exert beneficial effects on the diabetic kidney. We explored the action of losartan on AKT-mTOR phosphorylation in glomeruli and podocytes. Diabetes mellitus was induced to Sprague-Dawley rats by streptozotocin. Five months later, the rats were commenced on losartan and euthanized 2 months later. Kidneys were processed for immunofluorescence studies. Glomeruli were isolated for Western blot analysis. Diabetes increased activated forms of AKT and mTOR both in glomeruli and podocytes. In diabetic rats, losartan decreased phosphorylated/activated forms of AKT (Thr308) and mTOR (Ser2448) in glomeruli but decreased only activated mTOR in podocytes. However, in both glomeruli and podocytes of healthy animals, an inverse pattern was evident. In conclusion, a new body of evidence indicates the differential activation of AKT-mTOR in glomeruli and podocytes of healthy and diabetic animals in response to losartan.

Indexed as

Disease Models, AnimalAnimalsDiabetes Mellitus, Type 1Diabetic NephropathiesKidney GlomerulusLosartanMalePhosphorylationProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleyStructure-Activity RelationshipTOR Serine-Threonine KinasesLosartanProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesAKTdiabetic nephropathylosartanmTORpodocytestype 1 diabetes

Identifiers

PMID23456824
PMCPMC3715326
OpenAlexW2134272208

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.