In vivo study of the utility of selective intra-arterial injection of thiopental for neuroprotection in reversible cerebral ischemia.

Degradable starch microsphere cerebral ischemia intra-arterial neuroprotection thiopental

Journal

Acta radiologica (Stockholm, Sweden : 1987)
ISSN: 1600-0455
Titre abrégé: Acta Radiol
Pays: England
ID NLM: 8706123

Informations de publication

Date de publication:
23 Oct 2023
Historique:
medline: 24 10 2023
pubmed: 24 10 2023
entrez: 24 10 2023
Statut: aheadofprint

Résumé

Neuroprotective agents are needed to reduce cerebral damage during surgical or neurointerventional procedures including stroke patients. To evaluate if thiopental can be used as a neuroprotective agent when injected intra-arterially in a transient ischemia model. In total, 24 rabbits were studied as four groups of six animals. Group 1 served as the control group. In group 2, transient ischemia was obtained by intracarotid administration of degradable starch microspheres (DSM). Group 3 was administered thiopental intra-arterially via the carotid artery. Group 4 (experimental group) received both thiopental and DSM intra-arterially. DSM and thiopental were administered through a microcatheter placed into the common carotid artery via the central ear artery access. After sacrifice, apoptotic cells in the cerebral tissues of the animals were evaluated in H&E and TUNEL stained slides. There was a significant increase in the number of apoptotic glial or neuronal cells in group 2 compared to the control group and group 3. The mean number of both the apoptotic neuronal cells (6.8 ± 2.1 vs. 2.5 ± 1.3, The intra-arterial administration of thiopental has a protective effect on both glial and neuronal cells during temporary cerebral ischemia in low doses.

Sections du résumé

BACKGROUND BACKGROUND
Neuroprotective agents are needed to reduce cerebral damage during surgical or neurointerventional procedures including stroke patients.
PURPOSE OBJECTIVE
To evaluate if thiopental can be used as a neuroprotective agent when injected intra-arterially in a transient ischemia model.
MATERIAL AND METHODS METHODS
In total, 24 rabbits were studied as four groups of six animals. Group 1 served as the control group. In group 2, transient ischemia was obtained by intracarotid administration of degradable starch microspheres (DSM). Group 3 was administered thiopental intra-arterially via the carotid artery. Group 4 (experimental group) received both thiopental and DSM intra-arterially. DSM and thiopental were administered through a microcatheter placed into the common carotid artery via the central ear artery access. After sacrifice, apoptotic cells in the cerebral tissues of the animals were evaluated in H&E and TUNEL stained slides.
RESULTS RESULTS
There was a significant increase in the number of apoptotic glial or neuronal cells in group 2 compared to the control group and group 3. The mean number of both the apoptotic neuronal cells (6.8 ± 2.1 vs. 2.5 ± 1.3,
CONCLUSION CONCLUSIONS
The intra-arterial administration of thiopental has a protective effect on both glial and neuronal cells during temporary cerebral ischemia in low doses.

Identifiants

pubmed: 37872692
doi: 10.1177/02841851231206503
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2841851231206503

Déclaration de conflit d'intérêts

Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Murat Gökten (M)

Department of Neurosurgery, Corlu State Hospital, Tekirdag, Turkey.

Osman Öcal (O)

Department of Radiology, Hacettepe University, Ankara, Turkey.
Department of Radiology, University Hospital, LMU Munich, Munich, Germany.

Can Sezer (C)

Department of Neurosurgery, Seyhan State Hospital, Adana, Turkey.

Selim Zırh (S)

Department of Histology, Binali Yıldırım University, Erzincan, Turkey.

Sevda Muftuoglu (S)

Department of Histology, Hacettepe University, Ankara, Turkey.

Elif Öcal (E)

Department of Radiology, University Hospital, LMU Munich, Munich, Germany.

Burcak Bilginer (B)

Department of Neurosurgery, Hacettepe University, Ankara, Turkey.

Anıl Arat (A)

Department of Radiology, Hacettepe University, Ankara, Turkey.

Classifications MeSH