Home > Journals > Journal of Neurosurgical Sciences > Past Issues > Journal of Neurosurgical Sciences 2017 August;61(4) > Journal of Neurosurgical Sciences 2017 August;61(4):380-7

CURRENT ISSUE
 

JOURNAL TOOLS

eTOC
To subscribe
Submit an article
Recommend to your librarian
 

ARTICLE TOOLS

Publication history
Reprints
Permissions
Cite this article as

 

ORIGINAL ARTICLE   

Journal of Neurosurgical Sciences 2017 August;61(4):380-7

DOI: 10.23736/S0390-5616.16.03068-X

Copyright © 2014 EDIZIONI MINERVA MEDICA

language: English

Dipyrone attenuates cerebral vasospasm after experimental subarachnoid hemorrhage in rabbits

Gökalp SILAV 1, Hakan ERGÜN 2, Habibullah DOLGUN 3, Tanzer SANCAK 4, Mustafa F. SARGON 5, Nihat EGEMEN 6

1 Department of Neurosurgery, Faculty of Medicine, Medipol University, Istanbul, Turkey; 2 Department of Pharmacology, Faculty of Medicine, Ankara University, Ankara, Turkey; 3 Department of Neurosurgery, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey; 4 Department of Radiology, Faculty of Medicine, Ankara University, Ankara, Turkey; 5 Department of Anatomy, Faculty of Medicine, Hacettepe University, Ankara, Turkey; 6 Department of Neurosurgery, Faculty of Medicine, Ankara University, Ankara, Turkey


PDF


BACKGROUND: The purpose of this study was to evaluate the effect of the systemic administration of dipyrone in a triple subarachnoid hemorrhage (SAH) model of cerebral vasospasm in rabbits.
METHODS: Experimental subarachnoid hemorrhage was induced in rabbits by injecting autologous arterial blood into the cisterna magna. Digital subtraction angiographies (DSA) were performed before and after the first experimental SAH, and at 30, 45, 60 minutes and 72 hours after the first drug administration to measure the diameter of basilar artery. Intracisternal blood injections were repeated 24 and 48 hours after the first injection. Dipyrone (N.=20) or 0.9% NaCl (N.=20) was administered intravenously after initial SAH induction and repeated at 8-hour intervals intramuscularly. After sacrificing by perfusion-fixation, basilar arteries were removed and sectioned for transmission electron microscopic (TEM) examination.
RESULTS: The average basilar artery diameter measured by DSA was 724±19 μm in the control, and 686±29 μm in treatment group before SAH. After SAH, mean basilar artery diameters decreased to 71% and 68% of their basal values, respectively. Dipyrone significantly attenuated the basilar artery diameter at one and 72 hours after the first drug administration, in comparison to the control group. TEM studies showed more edema in the endothelial cells of the basilar arteries of the control group when compared to the treatment group.
CONCLUSIONS: Dipyrone showed a beneficial effect in autologous blood-induced basilar artery vasospasm in rabbits. These data support the idea that dipyrone can be a potential candidate drug to be tested in patients suffering from cerebral vasospasm secondary to subarachnoid hemorrhage.


KEY WORDS: Basilar artery - Intercranial vasospasm - Dipyrone - Rabbits

top of page