Acetazolamide Mitigates Intracranial Pressure Spikes Without Affecting Functional Outcome After Experimental Hemorrhagic Stroke.


Journal

Translational stroke research
ISSN: 1868-601X
Titre abrégé: Transl Stroke Res
Pays: United States
ID NLM: 101517297

Informations de publication

Date de publication:
08 2019
Historique:
received: 29 08 2018
accepted: 04 09 2018
pubmed: 19 9 2018
medline: 17 1 2020
entrez: 19 9 2018
Statut: ppublish

Résumé

Increased intracranial pressure (ICP) after stroke can lead to poor outcome and death. Novel treatments to combat ICP rises are needed. The carbonic anhydrase inhibitor acetazolamide diminishes cerebrospinal fluid (CSF) production, reduces ICP in healthy animals, and is beneficial for idiopathic intracranial hypertension patients. We tested whether acetazolamide mitigates ICP elevations by presumably decreasing CSF volume after collagenase-induced striatal hemorrhage in rats. We confirmed that acetazolamide did not adversely affect hematoma formation in this model or physiological variables, such as temperature. Then, we assessed the effects of acetazolamide on ICP. Lastly, we tested the effects of acetazolamide on behavioral and histological outcome. Acetazolamide reduced the magnitude and occurrence of short-timescale ICP spikes, assessed as disproportionate increases in ICP (sudden ICP increases > 10 mmHg), 1-min peak ICP, and the magnitude of spikes > 20 mmHg. However, mean ICP was unaffected. In addition, acetazolamide reduced ICP variability, reflecting improved intracranial compliance. Compliance measures were strongly correlated with high peak and mean ICP, whereas ipsilateral hemisphere water content was not correlated with ICP. Despite effects on ICP, acetazolamide did not improve behavioral function or affect lesion size. In summary, we show that intracerebral hemorrhage creates an impaired compliance state within the cranial space that can result in large, transient ICP spikes. Acetazolamide ameliorates intracranial compliance and mitigates ICP spikes, but does not improve functional outcome, at least for moderate-severity ICH in rats.

Identifiants

pubmed: 30225552
doi: 10.1007/s12975-018-0663-6
pii: 10.1007/s12975-018-0663-6
pmc: PMC6647499
doi:

Substances chimiques

Carbonic Anhydrase Inhibitors 0
Acetazolamide O3FX965V0I

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

428-439

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Auteurs

Michael R Williamson (MR)

Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Canada.

Cassandra M Wilkinson (CM)

P217 Biological Sciences Building, Department of Psychology, University of Alberta, Edmonton, AB, T6G 2E9, Canada.

Kristen Dietrich (K)

Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Canada.

Frederick Colbourne (F)

Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Canada. fcolbour@ualberta.ca.
P217 Biological Sciences Building, Department of Psychology, University of Alberta, Edmonton, AB, T6G 2E9, Canada. fcolbour@ualberta.ca.

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