Publication:
Morphological changes in striated muscle fibers caused by components of the Thiel embalming method.

cris.virtual.author-orcid0000-0002-5062-1169
cris.virtualsource.author-orcid311d14ec-3316-4b43-a112-9afb157be4e4
cris.virtualsource.author-orcid93b0d2fb-72fb-4472-99ad-96f2f50b35ca
cris.virtualsource.author-orcid55b10bd4-9d87-49f2-adf4-6c2bd4ffdc72
cris.virtualsource.author-orcid7e76a811-24e7-4722-8fd1-76e8d85ea63f
cris.virtualsource.author-orcid50f55964-7ff8-4bc0-8549-9919a3cbee93
cris.virtualsource.author-orcidd3cbdc26-1ec0-4b74-b87d-c2aa72202b03
datacite.rightsmetadata.only
dc.contributor.authorAaldijk, Dea
dc.contributor.authorReusser, Adrian
dc.contributor.authorEppler, Elisabeth
dc.contributor.authorYao, Eveline
dc.contributor.authorDjonov, Valentin Georgiev
dc.contributor.authorHalm, Sebastian
dc.date.accessioned2024-10-25T15:39:11Z
dc.date.available2024-10-25T15:39:11Z
dc.date.issued2024
dc.description.abstractBACKGROUND Thiel-fixed body donors are highly valued for surgical training courses. The pronounced flexibility of Thiel-fixed tissue has been postulated to be caused by histologically visible fragmentation of striated muscle. The aim of this study was to analyze whether a specific ingredient, pH, decay, or autolysis could cause this fragmentation in order to modulate the Thiel solution to adapt specimen flexibility specifically to the needs of different courses. MATERIALS AND METHODS Striated muscle of the mouse was fixed for different time periods in formalin, Thiel solution, and its individual ingredients, and analysed by light microscopy. Further, pH-values of Thiel solution and its ingredients were measured. In addition, unfixed muscle tissue was histologically analyzed including Gram staining to investigate a relationship between autolysis, decomposition, and fragmentation. RESULTS Muscle fixed with Thiel solution for three months was slightly more fragmentated than muscle fixed for 1 day. Fragmentation was more pronounced after one year of immersion. Three individual salt ingredients showed slight fragmentation. Decay and autolysis had no effect on fragmentation, which occurred regardless of the pH of all solutions. CONCLUSIONS Fragmentation of Thiel-fixed muscle is dependent on fixation time and most likely occurs due to salts present in the Thiel solution. Adjustment of the salt composition in the Thiel solution with verification of the influence on the fixation effect, fragmentation and flexibility of the cadavers could be performed in further studies.
dc.description.numberOfPages9
dc.description.sponsorshipInstitut für Anatomie
dc.description.sponsorshipInstitut für Anatomie - Topographische & Klinische Anatomie
dc.description.sponsorshipMicroscopy Imaging Center (MIC)
dc.identifier.pmid36811140
dc.identifier.publisherDOI10.5603/FM.a2023.0010
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/164330
dc.language.isoen
dc.publisherVia Medica
dc.relation.ispartofFolia morphologica
dc.relation.issn1644-3284
dc.relation.organizationInstitute of Anatomy
dc.relation.organizationInstitute of Anatomy, Topographical and Clinical Anatomy
dc.subjectboric acid formalin fragmentation light microscopy pH saturated salt solution skeletal muscle tissue fixation
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.titleMorphological changes in striated muscle fibers caused by components of the Thiel embalming method.
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage91
oaire.citation.issue1
oaire.citation.startPage83
oaire.citation.volume83
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie - Topographische & Klinische Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliation2Institut für Anatomie
unibe.additional.sponsorshipMicroscopy Imaging Center (MIC)
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.description.ispublishedpub
unibe.eprints.legacyId179041
unibe.refereedtrue
unibe.subtype.articlejournal

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