Evidence map›Paper›PMID 31512044›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2019

Effect of topical administration of the microneurotrophin BNN27 in the diabetic rat retina.

Ruth Ibán-Arias, Silvia Lisa, Smaragda Poulaki, Niki Mastrodimou, Ioannis Charalampopoulos, Achille Gravanis, Kyriaki Thermos

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Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

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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

7 authors.

Ruth Ibán-AriasDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Silvia LisaDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Smaragda PoulakiDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Niki MastrodimouDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Ioannis CharalampopoulosDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Achille GravanisDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece.
Kyriaki ThermosDepartment of Pharmacology, School of Medicine, University of Crete, 70013, Heraklion, Crete, Greece. thermos@uoc.gr.ORCID http://orcid.org/0000-0003-0187-9048

Funding

European Social Fund 3948
6 · The paper itself

Abstract

purposeDiabetic retinopathy (DR) is a complex eye disease associated with diabetes mellitus. It is characterized by three pathophysiological components, namely microangiopathy, neurodegeneration, and inflammation. We recently reported that intraperitoneal administration of BNN27, a novel neurosteroidal microneurotrophin, reversed the diabetes-induced neurodegeneration and inflammation in rats treated with streptozotocin (STZ), by activating the NGF TrkA and p75 receptors. The aim of the present study was to investigate the efficacy of BNN27 to protect retinal neurons when applied topically as eye drops in the same model.

methodsThe STZ rat model of DR was employed. BNN27 was administered as eye drops to diabetic Sprague-Dawley rats for 7 days, 4 weeks post-STZ (70 mg/kg) injection. Immunohistochemistry and western blot analyses were employed to examine the viability of retinal neurons in control, diabetic, and diabetic-treated animals and the involvement of the TrkA receptor and its downstream signaling ERK1/2 kinases, respectively.

resultsBNN27 reversed the STZ-induced attenuation of the immunoreactive brain nitric oxide synthetase (bNOS)- and tyrosine hydroxylase (TH)-expressing amacrine cells and neurofilament (NFL)-expressing ganglion cell axons in a dose-dependent manner. In addition, BNN27 activated/phosphorylated the TrkA receptor and its downstream prosurvival signaling pathway, ERK1/2 kinases.

conclusionsThe results of this study provide solid evidence regarding the efficacy of BNN27 as a neuroprotectant to the diabetic retina when administered topically, and suggest that its pharmacodynamic and pharmacokinetic profiles render it a putative therapeutic for diabetic retinopathy.

Indexed as

Diabetes Mellitus, ExperimentalAdministration, TopicalAnimalsBlotting, WesternDehydroepiandrosteroneDiabetic RetinopathyDose-Response Relationship, DrugFemaleMaleRatsRats, Sprague-DawleyRetinaTreatment OutcomeBNN27 compoundDehydroepiandrosteroneERK1/2 kinasesNerve growth factorNeurodegenerationNeuroprotectionRetinal diseaseTrkA receptor

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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.