Evidence map›Paper›PMID 25786435›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2015

Structural analysis of alterations in zebrafish muscle differentiation induced by simvastatin and their recovery with cholesterol.

Laise M Campos, Eduardo A Rios, Victor Midlej, Georgia C Atella, Suzana Herculano-Houzel, Marlene Benchimol, Claudia Mermelstein, Manoel Luís Costa

Open access · hybridAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 21 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

8 authors at 2 institutions in 1 country.

Laise M CamposInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, RJ, Brazil (LMC,EAR,SHH,CM,MLC)
Eduardo A RiosInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, RJ, Brazil (LMC,EAR,SHH,CM,MLC)
Victor MidlejLaboratório de Ultraestrutura Celular, Universidade Santa Úrsula, RJ, Brazil (VM,MB)
Georgia C AtellaInstituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro, RJ, Brazil (GCA)
Suzana Herculano-HouzelInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, RJ, Brazil (LMC,EAR,SHH,CM,MLC)
Marlene BenchimolLaboratório de Ultraestrutura Celular, Universidade Santa Úrsula, RJ, Brazil (VM,MB)
Claudia MermelsteinInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, RJ, Brazil (LMC,EAR,SHH,CM,MLC)
Manoel Luís CostaInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, RJ, Brazil (LMC,EAR,SHH,CM,MLC)
Universidade Santa Úrsula · BRUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro studies show that cholesterol is essential to myogenesis. We have been using zebrafish to overcome the limitations of the in vitro approach and to study the sub-cellular structures and processes involved during myogenesis. We use simvastatin--a drug widely used to prevent high levels of cholesterol and cardiovascular disease--during zebrafish skeletal muscle formation. Simvastatin is an efficient inhibitor of cholesterol synthesis that has various myotoxic consequences. Here, we employed simvastatin concentrations that cause either mild or severe morphological disturbances to observe changes in the cytoskeleton (intermediate filaments and microfilaments), extracellular matrix and adhesion markers by confocal microscopy. With low-dose simvastatin treatment, laminin was almost normal, and alpha-actinin was reduced in the myofibrils. With high simvastatin doses, laminin and vinculin were reduced and appeared discontinuous along the septa, with almost no myofibrils, and small amounts of desmin accumulating close to the septa. We also analyzed sub-cellular alterations in the embryos by electron microscopy, and demonstrate changes in embryo and somite size, septa shape, and in myofibril structure. These effects could be reversed by the addition of exogenous cholesterol. These results contribute to the understanding of the mechanisms of action of simvastatin in muscle cells in particular, and in the study of myogenesis in general.

Indexed as

AnimalsCholesterolHypolipidemic AgentsMuscle DevelopmentMuscle, SkeletalMyofibrilsSimvastatinZebrafishCholesterolHypolipidemic AgentsSimvastatincell adhesiondesminmyofibrilsmyogenesissimvastatinzebrafish embryos

Identifiers

PMID25786435
PMCPMC4872197
OpenAlexW2093176616

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.