Evidence map›Paper›PMID 36613769›Full record

ArticleInternational journal of molecular sciences2022

Characterization of Diabetic Retinopathy in Two Mouse Models and Response to a Single Injection of Anti-Vascular Endothelial Growth Factor.

Tamar Azrad-Leibovich, Alon Zahavi, Moran Friedman Gohas, Myles Brookman, Orit Barinfeld, Orkun Muhsinoglu, Shalom Michowiz, Dror Fixler, Nitza Goldenberg-Cohen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
2.7field-weighted citation impact, top 10% 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, 14 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

9 authors at 4 institutions in 1 country.

Tamar Azrad-LeibovichKrieger Eye Research Laboratory, Felsenstein Medical Research Center, Petach Tikva 4941492, Israel.
Alon ZahaviSackler Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0000-0002-9451-5253
Moran Friedman GohasKrieger Eye Research Laboratory, Felsenstein Medical Research Center, Petach Tikva 4941492, Israel.
Myles BrookmanSackler Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.
Orit BarinfeldKrieger Eye Research Laboratory, Felsenstein Medical Research Center, Petach Tikva 4941492, Israel.
Orkun MuhsinogluKrieger Eye Research Laboratory, Felsenstein Medical Research Center, Petach Tikva 4941492, Israel.
Shalom MichowizDepartment of Neurosurgery, Rabin Medical Center-Beilinson Hospital, Petach Tikva 4941492, Israel.
Dror FixlerFaculty of Engineering and Institute of Nanotechonology and Advanced Materials, Bar Ilan University, Ramat Gan 5200100, Israel.ORCID 0000-0003-0963-7908
Nitza Goldenberg-CohenKrieger Eye Research Laboratory, Felsenstein Medical Research Center, Petach Tikva 4941492, Israel.ORCID 0000-0002-5648-1873
Tel Aviv University · ILBar-Ilan University · ILRabin Medical Center · ILTechnion – Israel Institute of Technology · IL

Funding

CSRD VA 1D-CURE, ISRAEL MINISTRY OF HEALTH AND ISRAEL SCIENTIFIC FOUNDATION, Jerusalem, Israel 3-0000-11401
6 · The paper itself

Abstract

In this study, we characterized diabetic retinopathy in two mouse models and the response to anti-vascular endothelial growth factor (VEGF) injection. The study was conducted in 58 transgenic, non-obese diabetic (NOD) mice with spontaneous type 1 diabetes (n = 30, DMT1-NOD) or chemically induced (n = 28, streptozotocin, STZ-NOD) type 1 diabetes and 20 transgenic db/db mice with type 2 diabetes (DMT2-db/db); 30 NOD and 8 wild-type mice served as controls. Mice were examined at 21 days for vasculopathy, retinal thickness, and expression of genes involved in oxidative stress, angiogenesis, gliosis, and diabetes. The right eye was histologically examined one week after injection of bevacizumab, ranibizumab, saline, or no treatment. Flat mounts revealed microaneurysms and one apparent area of tufts of neovascularization in the diabetic retina. Immunostaining revealed activation of Müller glia and prominent Müller cells. Mean retinal thickness was greater in diabetic mice. RAGE increased and GFAP decreased in DMT1-NOD mice; GFAP and SOX-9 mildly increased in db/db mice. Anti-VEGF treatment led to reduced retinal thickness. Retinas showed vasculopathy and edema in DMT1-NOD and DMT2-db/db mice and activation of Müller glia in DMT1-NOD mice, with some response to anti-VEGF treatment. Given the similarity of diabetic retinopathy in mice and humans, comparisons of type 1 and type 2 diabetic mouse models may assist in the development of new treatment modalities.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Diabetic RetinopathyAnimalsDisease Models, AnimalHumansMiceMice, Inbred NODRetinaVascular Endothelial Growth Factor AVascular Endothelial Growth FactorsVascular Endothelial Growth Factor AVascular Endothelial Growth Factorsanti-vascular endothelial growth factordiabetic retinopathyneovascularizationtransgenic mice

Identifiers

PMID36613769
PMCPMC9820807
OpenAlexW4313244758

What OpenQuestion holds

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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.