Evidence map›Paper›PMID 36881303›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Generating Widespread and Scalable Retinal Lesions in Adult Zebrafish by Intraocular Injection of Ouabain.

Diana M Mitchell, Deborah L Stenkamp

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
6.9field-weighted citation impact, top 4% 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

6 citing papers in PubMed, 6 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

2 authors at 1 institution in 1 country.

Diana M MitchellDepartment of Biological Sciences, University of Idaho, Moscow, ID, USA. dmitchell@uidaho.edu.
Deborah L StenkampDepartment of Biological Sciences, University of Idaho, Moscow, ID, USA. dstenkam@uidaho.edu.
University of Idaho · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
Patterning Genes in Retinal DevelopmentR01EY012146 · NEI · UNIVERSITY OF IDAHO · PI Deborah L Stenkamp · 2004 to 2026
$6.7M
Macrophage Determinants of Retinal RegenerationR01EY030467 · NEI · UNIVERSITY OF IDAHO · PI MITCHELL, DIANA · 2020 to 2024
$1.8M
Acquisition of a Dynamic Imaging SystemS10OD018044 · OD · UNIVERSITY OF IDAHO · PI STENKAMP, DEBORAH L · 2014 to 2014
$455k
Synapses in Regenerated RetinaR21EY026814 · NEI · UNIVERSITY OF IDAHO · PI STENKAMP, DEBORAH L · 2016 to 2017
$388k
NEI NIH HHS R01 EY012146NEI NIH HHS R01 EY030467NEI NIH HHS R21 EY026814NIGMS NIH HHS P20 GM103408NIH HHS S10 OD018044
6 · The paper itself

Abstract

Zebrafish regenerate functional retinal neurons after injury. Regeneration takes place following photic, chemical, mechanical, surgical, or cryogenic lesions, as well as after lesions that selectively target specific neuronal cell populations. An advantage of chemical retinal lesion for studying the process of regeneration is that the lesion is topographically widespread. This results in the loss of visual function as well as a regenerative response that engages nearly all stem cells (Müller glia). Such lesions can therefore be used to further our understanding of the process and mechanisms underlying re-establishment of neuronal wiring patterns, retinal function, and visually mediated behaviors. Widespread chemical lesions also permit the quantitative analysis of gene expression throughout the retina during the period of initial damage and over the duration of regeneration, as well as the study of growth and targeting of axons of regenerated retinal ganglion cells. The neurotoxic Na+/K+ ATPase inhibitor ouabain specifically offers a further advantage over other types of chemical lesions in that it is scalable; the extent of damage can be targeted to include only inner retinal neurons, or all retinal neurons, simply by adjusting the intraocular concentration of ouabain that is used. Here we describe the procedure through which these "selective" vs. "extensive" retinal lesions can be generated.

Indexed as

OuabainZebrafishAnimalsAxonsInjections, IntraocularNeurogliaOuabainCentral nervous systemEyeIntravitreal injectionLesionMüller gliaOuabainRegenerationRetinaZebrafish

Identifiers

PMID36881303
PMCPMC12068065
OpenAlexW4323347632

What OpenQuestion holds

Textmetadata
LicenceTDM
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.