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dc.contributor.authorRobert, SM
dc.contributor.authorReeves, BC
dc.contributor.authorAlper, SL
dc.contributor.authorZhang, J
dc.contributor.authorKahle, KT
dc.date.accessioned2020-10-06T08:00:07Z
dc.date.issued2020-08-20
dc.description.abstractIntroduction: Research has advanced our understanding of the molecular and cellular mechanisms of cerebral edema and has propelled the development of novel antiedema therapeutics. Current evidence supports aberrant neuro-glial ion transport as a central mechanism that underlies pathological fluid accumulation after central nervous system injury. Areas covered: Novel agents in clinical development show potential in altering the natural history and treatment of cerebral edema. Using the PubMed and Google Scholar databases, we review recent advances in our understanding of cerebral edema and describe agents under active investigation, their mechanism, and their application in recent and ongoing clinical trials. Expert opinion: Pharmacotherapies that target molecular mechanisms underlying the compensatory post-injury response of ion channels and transporters that lead to pathological alteration of osmotic gradients are the most promising therapeutic strategies. Repurposing of drugs such as glyburide that inhibit the aberrant upregulation of ion channels such as SUR1-TRPM4, and novel agents, such as ZT-1a, which reestablish physiological regulation of ion channels such as NKCC1/KCC, could be useful adjuvants to prevent and even reverse fluid accumulation in the brain parenchyma.en_GB
dc.identifier.citationPublished online 20 August 2020en_GB
dc.identifier.doi10.1080/13543784.2020.1813715
dc.identifier.urihttp://hdl.handle.net/10871/123109
dc.language.isoenen_GB
dc.publisherTaylor & Francisen_GB
dc.rights.embargoreasonUnder embargo until 20 August 2021 in compliance with publisher policyen_GB
dc.rights© 2020 Informa UK Limited, trading as Taylor & Francis Group.en_GB
dc.titleNew drugs on the horizon for cerebral edema: what’s in the clinical development pipeline?en_GB
dc.typeArticleen_GB
dc.date.available2020-10-06T08:00:07Z
dc.identifier.issn1354-3784
dc.descriptionThis is the author accepted manuscript. the final version is available from Taylor & Francis via the DOI in this recorden_GB
dc.identifier.journalExpert Opinion on Investigational Drugsen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2020-08-19
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2020-08-20
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-10-06T07:56:12Z
refterms.versionFCDAM
refterms.panelAen_GB


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