Evidence map›Paper›PMID 19629513›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2009

Longer lasting electroretinographic recordings from the isolated and superfused murine retina.

Walid Albanna, Mohammed Banat, Nadeen Albanna, Maged Alnawaiseh, Sergej A Siapich, Peter Igelmund, Marco Weiergräber, Matthias Lüke, Toni Schneider

Abstract read
PubMed Publisher
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Organ Cultures for Retinal Diseases.Frontiers in neuroscience · 2020
    Review
  3. Article
  4. Low concentrations of ethanol but not of dimethyl sulfoxide (DMSO) impair reciprocal retinal signal transduction.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2015
    Article
  5. Article
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 2 institutions in 1 country.

Walid AlbannaInstitute of Neurophysiology, University of Cologne, Robert-Koch-Strasse 39, Köln, Germany.
Mohammed Banat
Nadeen Albanna
Maged Alnawaiseh
Sergej A Siapich
Peter Igelmund
Marco Weiergräber
Matthias Lüke
Toni Schneider
University of Cologne · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnalysis of retinal signaling in mutant mice has become a powerful tool for studying retinal function and disease. Previous attempts to record from isolated mouse retina have been limited to short time periods (about 90 min). It would be desirable to achieve longer-lasting recordings comparable to those that have been performed in larger vertebrates such as rat, rabbit, cat, and bovine (up to 10 h). We performed a series of recordings from isolated mouse retina under a number of different conditions in order to determine the optimal parameters for this species.

methodsWe used a superfused vertebrate retina assay, for which the murine retina had to be isolated with specific tools. Subsequently, the ERG recordings were optimized for nutrient solution, incubation temperature, and flash light intensity.

resultsTo improve the sensitivity and stability of photoreceptor and retinal network responses from the isolated and superfused murine retina, two different nutrient solutions from rat (physiological Ca(2+)) and bovine (reduced Ca(2+) but increased phosphate buffering capacity) were used. Further, a temperature reduced to 27.5 degrees C, a light intensity ten-fold increased (63 mlux), and an increased flow rate (2 ml/min) provided conditions under which the b-wave response was stable for more than 3 hours. Well-known Ca(2+) channel antagonists (isradipine and NiCl(2)) were tested for their potency to antagonize transretinal signalling.

conclusionIn conclusion, the isolated murine retina can be used as a pharmacological testing system, which provides the additional advantage of selective gene inactivation for better understanding of retinal signalling.

Indexed as

ElectroretinographyMiceAnimalsCalcium Channel BlockersCattleDose-Response Relationship, RadiationFoodIn Vitro TechniquesIsradipineLightMice, Inbred StrainsNickelOxygenPerfusionPhotic StimulationPhotoreceptor Cells, VertebrateCalcium Channel BlockersIsradipineNickelnickel chlorideOxygenSolutions

Identifiers

PMID19629513
OpenAlexW1984484827

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.