Evidence map›Paper›PMID 26335534›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2016

Investigating short-term toxicity of melphalan in a model of an isolated and superfused bovine retina.

Kai Januschowski, Carlo Krupp, Sebastian Mueller, Kathleen Hofmann, Sven Schnichels, Ulrike Hagemann, Martin S Spitzer, Karl-Ulrich Bartz-Schmidt, Sabine Aisenbrey

Abstract read
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In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Kai JanuschowskiCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany. Kai.januschowski@med.uni-tuebingen.de.
Carlo KruppCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Sebastian MuellerCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Kathleen HofmannCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Sven SchnichelsCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Ulrike HagemannCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Martin S SpitzerCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Karl-Ulrich Bartz-SchmidtCentre for Ophthalmology, University Eye Hospital Tübingen, Schleichstr. 12, D-72076, Tübingen, Germany.
Sabine AisenbreyUniversity Eye Hospital, University of Oldenburg, Oldenburg, Germany.
STZ eyetrial · DECarl von Ossietzky Universität Oldenburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMelphalan, as a treatment for retinoblastoma, has been applied intra-arterially by catheterisation of the ophthalmic artery or intravitreally, aiming to reduce systemic side effects of intravenous drug therapy. This study evaluates retinal toxicity of different melphalan concentrations measured by electroretinogram (ERG) in an isolated and perfused retinal whole mount culture.

methodsFor functional testing, bovine retinas were prepared and perfused with an oxygen-saturated standard solution and the ERG was recorded until stable b-wave or a-wave amplitudes were reached. Thereafter, retinae were exposed to 80, 160 and 320 μg/ml of melphalan for 30 min. After exposure, a washout was performed thrice for 5 min each and the ERG amplitude recovery was monitored for 60 min. To investigate the effects on photoreceptor function, 1-mM asparate was added to suppress the b-wave and obtain isolated a-waves.

resultsWhile no toxic effects for a concentration of 80 μg/ml were observed, both b- and a-waves were significantly reduced after application of 160 (b-wave 43.8 %, p = 0.03; a-wave 28.2 %, p = 0.04) and 320 μg/ml (b-wave 20.0 %, p = 0.04; a-wave 35.8 %, p = 0.02). For 320 μg/ml, this reduction remained significant at the end of the washout (b-wave 40.0 % p = 0.02; a-wave 26.4 %, p = 0.02).

conclusionsEpiretinal or intraretinal concentrations of 80-μg/ml melphalan do not cause toxic effects in this in vitro model. Concentrations higher than 160 μg/ml should be avoided.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingAspartic AcidCattleDark AdaptationElectroretinographyMelphalanOrgan Culture TechniquesPhotic StimulationPhotoreceptor Cells, VertebrateRetinaRetinal Ganglion CellsAntineoplastic Agents, AlkylatingAspartic AcidMelphalanElectroretinogramMelphalanRetinaRetinal toxicityRetinoblastoma

Identifiers

PMID26335534
OpenAlexW1241243741

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.