Publication:
Experimental subarachnoid haemorrhage models in rats

dc.contributor.authorKanpolat, Y.
dc.contributor.buuauthorAlkan, Tülin
dc.contributor.buuauthorKorfalı, Ender
dc.contributor.buuauthorKahveci, Nevzat
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentNöroloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-0841-8201
dc.contributor.researcheridAAG-7070-2021
dc.contributor.scopusid6601953747
dc.contributor.scopusid7004641343
dc.contributor.scopusid6602597846
dc.date.accessioned2022-10-07T06:57:58Z
dc.date.available2022-10-07T06:57:58Z
dc.date.issued2002
dc.descriptionBu çalışma, 2001 yılında Antalya'da düzenlenen Conference on Research and Publishing Neurosurgery'da bildiri olarak sunulmuştur.
dc.description.abstractThere is no comprehensive and reliable model available in small animals that are suitable for the study of subarachnoid haemorrhage (SAH). In the study we reviewed the advantages and disadvantages of available SAH models in rats and presented our model. Experimental SAH was induced in a group of 350-450 g SpragueDawley rats. A 2 mm-diameter burr hole was drilled and, working under a microscope, haemorrhage was produced by transclival puncture of the basilar artery with a 20 mum thick piece of glass. The rats were assigned to either the experimental group (n: 7) or the control group (n: 7). Local cerebral blood flow (LCBF), intracranial pressure (ICP), and cerebral perfusion pressure (CPP) were measured for 60 min after SAH, after which the rats were decapitated. Microscopic examinations were done on three different segments of the basilar artery. There was a significant and sharp drop in LCBF just after SAH was induced (56.17 +/- 12.80 mILD/min/100 g and 13.57 +/- 5.85 mILD/min/100 g for baseline and post-SAH, respectively; p < 0.001), the flow slowly increased by the end of the experiment but never recovered to pre-SAH values (43,63 +/- 7.6 mILD/min/ 100 g, p < 0.05). ICP (baseline 7.33 +/- 0.8 mmHg) increased acutely to 70.6 +/- 9.2 mmHg, and also returned to normal levels by 60 min after SAH. CPP (baseline 75.1 +/- 4.9 mmHg) dropped accordingly (to 21.0 +/- 6.3 mmHg) and then increased, reaching 70.1 +/- 4.9 mmHg at 60 min after SAH. Examinations of the arteries revealed decreased inner luminal diameter and distortion of the elastica layer. We present an inexpensive and reliable model of SAH in the rat that allows single and multiple haemorrhages and to study the early and late course of pathological changes.
dc.description.sponsorshipEuropean Association of Neurosurgical Societies
dc.identifier.citationAlkan, T. vd. (2002). "Experimental subarachnoid haemorrhage models in rats". Ed. Kanpolat, Y. Acta Neurochirurgica Supplement, Research and Publishing in Neurosurgery, 83, 61-69.
dc.identifier.endpage69
dc.identifier.issn0065-1419
dc.identifier.pubmed12442623
dc.identifier.scopus2-s2.0-0036436266
dc.identifier.startpage61
dc.identifier.urihttps://doi.org/10.1007/978-3-7091-6743-4_11
dc.identifier.urihttps://link.springer.com/chapter/10.1007/978-3-7091-6743-4_11
dc.identifier.urihttp://hdl.handle.net/11452/29017
dc.identifier.volume83
dc.identifier.wos000180585100011
dc.indexed.scopusScopus
dc.indexed.wosCPCIS
dc.language.isoen
dc.publisherSpringer-Verlag Wien
dc.relation.journalResearch and Publishing in Neurosurgery
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAcute vasoconstriction
dc.subjectNeurosciences & neurology
dc.subjectCerebral blood flow
dc.subjectAnimal models
dc.subjectIntracranial pressure
dc.subjectSubarachnoid haemorrhage
dc.subjectCerebral blood-flow
dc.subjectCanine carotid arteries
dc.subjectIn-vivo angioplasty
dc.subjectBasılar Artery
dc.subjectPrimate model
dc.subjectAcute vasoconstriction
dc.subjectMorphological analyses
dc.subjectAnimal-Model
dc.subjectNitric-oxide
dc.subjectHemorrhage
dc.subject.emtreeMale
dc.subject.emtreeAnimal
dc.subject.emtreeArticle
dc.subject.emtreeBasilar artery
dc.subject.emtreeBlood flow
dc.subject.emtreeBlood pressure
dc.subject.emtreeBrain ischemia
dc.subject.emtreeBrain vasospasm
dc.subject.emtreeDisease model
dc.subject.emtreeHuman
dc.subject.emtreeIntracranial pressure
dc.subject.emtreePathology
dc.subject.emtreeSprague Dawley rat
dc.subject.emtreePathophysiology
dc.subject.emtreeSubarachnoid hemorrhage
dc.subject.emtreeReproducibility
dc.subject.emtreePuncture
dc.subject.emtreePhysiology
dc.subject.emtreeVertebrobasilar insufficiency
dc.subject.emtreeRat
dc.subject.meshPunctures
dc.subject.meshAnimals
dc.subject.meshBasilar artery
dc.subject.meshBlood pressure
dc.subject.meshBrain ischemia
dc.subject.meshDisease models, animal
dc.subject.meshHumans
dc.subject.meshIntracranial pressure
dc.subject.meshMale
dc.subject.meshRats
dc.subject.meshVasospasm, intracranial
dc.subject.meshVertebrobasilar insufficiency
dc.subject.meshReproducibility of results
dc.subject.meshRats, sprague-Dawley
dc.subject.meshRegional blood flow
dc.subject.meshSubarachnoid hemorrhage
dc.subject.scopusIntracranial Vasospasm; Subarachnoid Hemorrhage; Ictus
dc.subject.wosClinical neurology
dc.titleExperimental subarachnoid haemorrhage models in rats
dc.typeProceedings Paper
dc.wos.quartileN/A
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Nöroloji Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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