Evidence map›Paper›PMID 12764104›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2003

Increased expression of brain-derived neurotrophic factor preserves retinal function and slows cell death from rhodopsin mutation or oxidative damage.

Godwin Okoye, Joelle Zimmer, Jennifer Sung, Peter Gehlbach, Tye Deering, Hiroyuki Nambu, Sean Hackett, Michele Melia, Noriko Esumi, Donald J Zack and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
0.1field-weighted citation impact, top 67% 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

50 citing papers in PubMed, 3 citations in OpenAlex.

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  11. Controlled release of corticosteroid with biodegradable nanoparticles for treating experimental autoimmune uveitis.Journal of controlled release : official journal of the Controlled Release Society · 2019
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  16. CNTF Gene Therapy Confers Lifelong Neuroprotection in a Mouse Model of Human Retinitis Pigmentosa.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
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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 1 institution in 1 country.

Godwin OkoyeDepartment of Ophthalmology, Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-9277, USA.
Joelle Zimmer
Jennifer Sung
Peter Gehlbach
Tye Deering
Hiroyuki Nambu
Sean Hackett
Michele Melia
Noriko Esumi
Donald J Zack
Peter A Campochiaro
Johns Hopkins University · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Donald J. Zack · 1985 to 2026
$22.1M
PATHOGENIC MECHANISMS IN PROLIFERATIVE VITREORETINOPATHYR01EY005951 · NEI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CAMPOCHIARO, PETER A · 1985 to 2014
$7.5M
Treatment of Ocular Neovascularization by InhibitorsK08EY013420 · NEI · JOHNS HOPKINS UNIVERSITY · PI GEHLBACH, PETER LOUIS · 2001 to 2005
$1.1M
NEI NIH HHS EY05951NEI NIH HHS K08 EY013420NEI NIH HHS K08EY13420NEI NIH HHS P30 EY001765NEI NIH HHS P30EY1765NEI NIH HHS R01 EY005951
6 · The paper itself

Abstract

There are no effective treatments for inherited retinal degenerations, which are prevalent causes of visual disability. Several proteins promote the survival of various types of neurons, and increasing expression of one or more of these survival factors is a promising strategy for a new treatment. Studies examining the effects of intravitreous injections of brain-derived neurotrophic factor (BDNF) in models of inherited retinal degenerations have suggested that BDNF has little survival-promoting activity for photoreceptors. In this study, we generated double transgenic mice with doxycycline-inducible expression of BDNF in the retina. In a model of primary rod photoreceptor degeneration, expression of BDNF resulted in significant delay in photoreceptor cell death and maintenance of retinal function assessed by electroretinogram recordings. Expression of BDNF also caused strong protection of photoreceptors from oxidative damage-induced cell death. These data suggest that continuous expression of BDNF, unlike intravitreous injections, results in morphologic and functional benefit in animal models of inherited retinal degeneration. Double transgenic mice with inducible expression of survival factors provide valuable tools for selection of survival factor candidates for gene therapy.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorCell DeathCell SurvivalDisease Models, AnimalDoxycyclineGene Expression RegulationGene Transfer TechniquesHyperoxiaImmunohistochemistryMiceMice, Inbred C57BLMice, TransgenicMutationNerve Growth FactorsOxygenBrain-Derived Neurotrophic FactorDoxycyclineNerve Growth FactorsOxygenRhodopsinRNA, Messenger

Identifiers

PMID12764104
PMCPMC6741081
OpenAlexW1728476777

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.