dc.contributor.author |
Dean, Justin |
en |
dc.contributor.author |
Gunn, Alistair |
en |
dc.contributor.author |
Wassink, Guido |
en |
dc.contributor.author |
George, Sherly |
en |
dc.contributor.author |
Bennet, Laura |
en |
dc.date.accessioned |
2017-10-13T01:28:49Z |
en |
dc.date.available |
2006-06-21 |
en |
dc.date.issued |
2006-10-27 |
en |
dc.identifier.citation |
Neuroscience, 142(3):615-628, 27 Oct 2006 |
en |
dc.identifier.issn |
0306-4522 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/36035 |
en |
dc.description.abstract |
Central alpha-adrenergic receptor activity is important for fetal adaptation to hypoxia before birth. It is unclear whether it is also important during recovery. We therefore tested the hypothesis that an infusion of the specific α2-adrenergic receptor antagonist idazoxan (1 mg/kg/h i.v.) from 15 min to 4 h after profound hypoxia induced by 25 min umbilical cord occlusion in fetal sheep at 70% of gestation (equivalent to the 28–32 weeks in humans) would increase neural injury. After 3 days’ recovery, idazoxan infusion was associated with a significant increase in neuronal loss in the hippocampus (P<0.05), expression of cleaved caspase-3 (P<0.05), and numbers of activated microglia (P<0.05). There was no significant effect on other neuronal regions or on loss of O4-positive premyelinating oligodendrocytes in the subcortical white matter. Idazoxan was associated with an increase in evolving epileptiform electroencephalographic (EEG) transient activity after occlusion (difference at peak 2.5±1.0 vs. 11.7±4.7 counts/min, P<0.05) and significantly reduced average spectral edge frequency, but not EEG intensity, from 54 until 72 h after occlusion (P<0.05). Hippocampal neuronal loss was correlated with total numbers of epileptiform transients during idazoxan infusion (P<0.01; r2=0.7). In conclusion, endogenous inhibitory α2-adrenergic receptor activation after severe hypoxia appears to significantly limit evolving hippocampal damage in the immature brain. |
en |
dc.description.uri |
https://www.ncbi.nlm.nih.gov/pubmed/16376952 |
en |
dc.language |
English |
en |
dc.publisher |
Elsevier |
en |
dc.relation.ispartofseries |
Neuroscience |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://sherpa.ac.uk/romeo/issn/0306-4522/
https://www.elsevier.com/about/our-business/policies/sharing |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.title |
Endogenous alpha(2)-adrenergic receptor-mediated neuroprotection after severe hypoxia in preterm fetal sheep |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1016/j.neuroscience.2006.06.066 |
en |
pubs.issue |
3 |
en |
pubs.begin-page |
615 |
en |
pubs.volume |
142 |
en |
dc.rights.holder |
Copyright: Elsevier |
en |
dc.identifier.pmid |
16952424 |
en |
pubs.author-url |
http://www.sciencedirect.com/science/article/pii/S0306452206008712 |
en |
pubs.end-page |
628 |
en |
pubs.publication-status |
Published |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
66615 |
en |
pubs.org-id |
Medical and Health Sciences |
en |
pubs.org-id |
Medical Sciences |
en |
pubs.org-id |
Physiology Division |
en |
dc.identifier.eissn |
1873-7544 |
en |
pubs.record-created-at-source-date |
2010-09-01 |
en |
pubs.online-publication-date |
2006-09-06 |
en |
pubs.dimensions-id |
16952424 |
en |