Volatile anesthetics influence blood-brain barrier integrity by modulation of tight junction protein expression in traumatic brain injury

dc.contributor.authorThal, Serge
dc.contributor.authorLuh, Clara
dc.contributor.authorSchaible, Eva-Verena
dc.contributor.authorTimaru-Kast, Ralph
dc.contributor.authorHedrich, Jana
dc.contributor.authorLuhmann, Heiko
dc.contributor.authorEngelhard, Kristin
dc.contributor.authorZehendner, Christoph M.
dc.date.accessioned2013-01-31T15:51:33Z
dc.date.available2013-01-31T16:51:33Z
dc.date.issued2012
dc.description.abstractDisruption of the blood-brain barrier (BBB) results in cerebral edema formation, which is a major cause for high mortality after traumatic brain injury (TBI). As anesthetic care is mandatory in patients suffering from severe TBI it may be important to elucidate the effect of different anesthetics on cerebral edema formation. Tight junction proteins (TJ) such as zonula occludens-1 (ZO-1) and claudin-5 (cl5) play a central role for BBB stability. First, the influence of the volatile anesthetics sevoflurane and isoflurane on in-vitro BBB integrity was investigated by quantification of the electrical resistance (TEER) in murine brain endothelial monolayers and neurovascular co-cultures of the BBB. Secondly brain edema and TJ expression of ZO-1 and cl5 were measured in-vivo after exposure towards volatile anesthetics in native mice and after controlled cortical impact (CCI). In in-vitro endothelial monocultures, both anesthetics significantly reduced TEER within 24 hours after exposure. In BBB co-cultures mimicking the neurovascular unit (NVU) volatile anesthetics had no impact on TEER. In healthy mice, anesthesia did not influence brain water content and TJ expression, while 24 hours after CCI brain water content increased significantly stronger with isoflurane compared to sevoflurane. In line with the brain edema data, ZO-1 expression was significantly higher in sevoflurane compared to isoflurane exposed CCI animals. Immunohistochemical analyses revealed disruption of ZO-1 at the cerebrovascular level, while cl5 was less affected in the pericontusional area. The study demonstrates that anesthetics influence brain edema formation after experimental TBI. This effect may be attributed to modulation of BBB permeability by differential TJ protein expression. Therefore, selection of anesthetics may influence the barrier function and introduce a strong bias in experimental research on pathophysiology of BBB dysfunction. Future research is required to investigate adverse or beneficial effects of volatile anesthetics on patients at risk for cerebral edema.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin
dc.identifier.doihttp://doi.org/10.25358/openscience-741
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/743
dc.identifier.urnurn:nbn:de:hebis:77-33080
dc.language.isoeng
dc.rightsCC-BY-3.0de_DE
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleVolatile anesthetics influence blood-brain barrier integrity by modulation of tight junction protein expression in traumatic brain injuryen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.journal.issue12
jgu.journal.titlePLoS one
jgu.journal.volume7
jgu.organisation.departmentFB 04 Medizin
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativee50752
jgu.publisher.doi10.1371/journal.pone.0050752
jgu.publisher.issn1932-6203
jgu.publisher.namePLoS
jgu.publisher.placeLawrence, Kan.
jgu.publisher.urihttp://dx.doi.org/10.1371/journal.pone.0050752
jgu.publisher.year2012
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610
jgu.type.dinitypeArticle
jgu.type.resourceText
jgu.type.versionPublished versionen_GB
opus.affiliatedThal, Serge
opus.affiliatedLuh, Clara
opus.affiliatedSchaible, Eva-Verena
opus.affiliatedTimaru-Kast, Ralph
opus.affiliatedHedrich, Jana
opus.affiliatedLuhmann, Heiko
opus.affiliatedEngelhard, Kristin
opus.affiliatedZehendner, Christoph M.
opus.date.accessioned2013-01-31T15:51:33Z
opus.date.available2013-01-31T16:51:33
opus.date.modified2016-11-28T08:35:50Z
opus.identifier.opusid3308
opus.institute.number0403
opus.institute.number0418
opus.metadataonlyfalse
opus.organisation.stringFB 04: Medizin: Institut für Physiologie und Pathophysiologiede_DE
opus.organisation.stringFB 04: Medizin: Klinik für Anästhesiologiede_DE
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_GB

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