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dc.contributor.authorHollis J.H.en
dc.contributor.authorSamarasinghe T.en
dc.contributor.authorPhillips D.J.en
dc.contributor.authorRao S.en
dc.contributor.authorYu V.Y.H.en
dc.contributor.authorWalker A.M.en
dc.contributor.authorFeng S.Y.S.en
dc.date.accessioned2021-05-14T12:15:53Zen
dc.date.available2021-05-14T12:15:53Zen
dc.date.copyright2019en
dc.date.created20190307en
dc.date.issued2019-03-07en
dc.identifier.citationPhysiological Reports. 7 (4) (no pagination), 2019. Article Number: e13973. Date of Publication: February 2019.en
dc.identifier.issn2051-817X (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36185en
dc.description.abstractAs the comparative pathophysiology of perinatal infection in the fetus and newborn is uncertain, this study contrasted the cerebral effects of endotoxemia in conscious fetal sheep and newborn lambs. Responses to intravenous bacterial endotoxin (lipopolysaccharide, LPS) or normal saline were studied on three consecutive days in fetal sheep (LPS 1 mug/kg, n = 5; normal saline n = 5) and newborn lambs (LPS 2 mug/kg, n = 10; normal saline n = 5). Cerebro-vascular function was assessed by monitoring cerebral blood flow (CBF) and cerebral vascular resistance (CVR) over 12 h each day, and inflammatory responses were assessed by plasma TNF alpha (TNF-alpha), nitrate and nitrite concentrations. Brain injury was quantified by counting both resting and active macrophages in the caudate nucleus and periventricular white matter (PVWM). An acute cerebral vasoconstriction (within 1 h of LPS injection) occurred in both the fetus (DELTACVR +53%) and newborn (DELTACVR +63%); subsequently prolonged cerebral vasodilatation occurred in the fetus (DELTACVR -33%) in association with double plasma nitrate/nitrite concentrations, but not in the newborn. Abundant infiltration of activated macrophages was observed in both CN and PVWM at each age, with the extent being 2-3 times greater in the fetus (P < 0.001). In conclusion, while the fetus and newborn experience a similar acute disruption of the cerebral circulation after LPS, the fetus suffers a more prolonged circulatory disruption, a greater infiltration of activated macrophages, and an exaggerated susceptibility to brain injury.Copyright © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society.en
dc.languageEnglishen
dc.languageenen
dc.publisherAmerican Physiological Societyen
dc.titleEndotoxin-induced cerebral pathophysiology: differences between fetus and newborn. [Physiological Reports]en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.14814/phy2.13973en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid30785235 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30785235]en
dc.identifier.source626587359en
dc.identifier.institution(Feng, Samarasinghe, Yu, Walker) The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia (Feng, Rao) Neonatal Directorate, King Edward Memorial Hospital, Perth Children's Hospital, Subiaco, WA, Australia (Hollis) Department of Physiology, Monash University, Clayton, VIC, Australia (Phillips) Academic & Medical Portfolio, Epworth HealthCare, Richmond, VIC, Australia (Yu) Monash Newborn, Monash Medical Centre, Clayton, VIC, Australiaen
dc.description.addressA.M. Walker, The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia. E-mail: adrian.walker@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsBrain endotoxin fetus injury newbornen
dc.identifier.authoremailWalker A.M.; adrian.walker@monash.eduen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
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