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Article: Heterogeneous responses of aquaporin-4 in oedema formation in a replicated severe traumatic brain injury model in rats

TitleHeterogeneous responses of aquaporin-4 in oedema formation in a replicated severe traumatic brain injury model in rats
Authors
KeywordsAquaporin-4
Blood-brain barrier
Brain injuries
Brain oedema
Rats
Issue Date2001
Citation
Neuroscience Letters, 2001, v. 301, n. 1, p. 21-24 How to Cite?
AbstractAquaporin-4 (AQP4) is the most abundant water channel in the rat brain. In this study, the distribution pattern and mRNA expression levels of AQP4 were examined in a severe traumatic brain injury model by immunohistochemistry and reverse transcription-polymerase chain reaction. Oedema formation and blood-brain barrier (BBB) integrity were assessed by wet-dry weight measurements and immunostaining of endogenous IgG respectively. In the oedematous contusional cortex with impaired BBB integrity, negative immunostaining of AQP4 and down-regulation of its mRNA level were identified (P < 0.05) at 1 day post-injury, while in other oedamatous regions of the injured brain where BBB was intact, there was no significant change in the AQP4 expression level. This heterogeneous pattern of AQP4 responses can be interpreted as follows: focal brain injury (such as a contusion) with impaired BBB resulting in vasogenic oedema is associated with reduction of AQP4 expression, whereas, in cytotoxic oedema, associated with diffuse brain injury with intact BBB, changes in AQP4 expression are not significant. This study provides basic information for investigating new treatments for traumatic brain oedema. © 2001 Elsevier Science Ireland Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/325044
ISSN
2021 Impact Factor: 3.197
2020 SCImago Journal Rankings: 0.944
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKe, Changshu-
dc.contributor.authorPoon, Wai Sang-
dc.contributor.authorNg, Ho Keung-
dc.contributor.authorPang, Jesse Chung Sean-
dc.contributor.authorChan, Yung-
dc.date.accessioned2023-02-27T07:29:15Z-
dc.date.available2023-02-27T07:29:15Z-
dc.date.issued2001-
dc.identifier.citationNeuroscience Letters, 2001, v. 301, n. 1, p. 21-24-
dc.identifier.issn0304-3940-
dc.identifier.urihttp://hdl.handle.net/10722/325044-
dc.description.abstractAquaporin-4 (AQP4) is the most abundant water channel in the rat brain. In this study, the distribution pattern and mRNA expression levels of AQP4 were examined in a severe traumatic brain injury model by immunohistochemistry and reverse transcription-polymerase chain reaction. Oedema formation and blood-brain barrier (BBB) integrity were assessed by wet-dry weight measurements and immunostaining of endogenous IgG respectively. In the oedematous contusional cortex with impaired BBB integrity, negative immunostaining of AQP4 and down-regulation of its mRNA level were identified (P < 0.05) at 1 day post-injury, while in other oedamatous regions of the injured brain where BBB was intact, there was no significant change in the AQP4 expression level. This heterogeneous pattern of AQP4 responses can be interpreted as follows: focal brain injury (such as a contusion) with impaired BBB resulting in vasogenic oedema is associated with reduction of AQP4 expression, whereas, in cytotoxic oedema, associated with diffuse brain injury with intact BBB, changes in AQP4 expression are not significant. This study provides basic information for investigating new treatments for traumatic brain oedema. © 2001 Elsevier Science Ireland Ltd.-
dc.languageeng-
dc.relation.ispartofNeuroscience Letters-
dc.subjectAquaporin-4-
dc.subjectBlood-brain barrier-
dc.subjectBrain injuries-
dc.subjectBrain oedema-
dc.subjectRats-
dc.titleHeterogeneous responses of aquaporin-4 in oedema formation in a replicated severe traumatic brain injury model in rats-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S0304-3940(01)01589-0-
dc.identifier.pmid11239707-
dc.identifier.scopuseid_2-s2.0-0035937639-
dc.identifier.volume301-
dc.identifier.issue1-
dc.identifier.spage21-
dc.identifier.epage24-
dc.identifier.isiWOS:000167505200006-

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