Evidence map›Paper›PMID 28827737›Full record

ArticleScientific reports2017

Histological Evaluation of Diabetic Neurodegeneration in the Retina of Zucker Diabetic Fatty (ZDF) Rats.

Klaudia Szabó, Anna Énzsöly, Bulcsú Dékány, Arnold Szabó, Rozina I Hajdú, Tamás Radovits, Csaba Mátyás, Attila Oláh, Lenke K Laurik, Gábor M Somfai and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  17. Diabetic Retinopathy: From Animal Models to Cellular Signaling.International journal of molecular sciences · 2022
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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

13 authors.

Klaudia SzabóDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Anna ÉnzsölyDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Bulcsú DékányDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Arnold SzabóDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Rozina I HajdúDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Tamás RadovitsHeart and Vascular Center, Semmelweis University, Budapest, H-1085, Hungary.
Csaba MátyásHeart and Vascular Center, Semmelweis University, Budapest, H-1085, Hungary.
Attila OláhHeart and Vascular Center, Semmelweis University, Budapest, H-1085, Hungary.
Lenke K LaurikDepartment of Ophthalmology, Semmelweis University, Budapest, H-1085, Hungary.
Gábor M SomfaiDepartment of Ophthalmology, Semmelweis University, Budapest, H-1085, Hungary.
Béla MerkelyHeart and Vascular Center, Semmelweis University, Budapest, H-1085, Hungary.
Ágoston SzélDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary.
Ákos LukátsDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, H-1085, Hungary. lukatsakos@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In diabetes, retinal dysfunctions exist prior to clinically detectable vasculopathy, however the pathology behind these functional deficits is still not fully established. Previously, our group published a detailed study on the retinal histopathology of type 1 diabetic (T1D) rat model, where specific alterations were detected. Although the majority of human diabetic patients have type 2 diabetes (T2D), similar studies on T2D models are practically absent. To fill this gap, we examined Zucker Diabetic Fatty (ZDF) rats - a model for T2D - by immunohistochemistry at the age of 32 weeks. Glial reactivity was observed in all diabetic specimens, accompanied by an increase in the number of microglia cells. Prominent outer segment degeneration was detectable with changes in cone opsin expression pattern, without a decrease in the number of labelled elements. The immunoreactivity of AII amacrine cells was markedly decreased and changes were detectable in the number and staining of some other amacrine cell subtypes, while most other cells examined did not show any major alterations. Overall, the retinal histology of ZDF rats shows a surprising similarity to T1D rats indicating that despite the different evolution of the disease, the neuroretinal cells affected are the same in both subtypes of diabetes.

Indexed as

Amacrine CellsAnimalsApoptosisBlood GlucoseBody WeightDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diabetic NephropathiesDiabetic RetinopathyDisease Models, AnimalMaleMice, TransgenicMicrogliaPhotoreceptor CellsRatsRats, ZuckerBlood Glucose

Identifiers

PMID28827737
PMCPMC5566374

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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.