Magnetic resonance imaging in experimental subarachnoid haemorrhage
We developed an MRI protocol to measure cerebrovascular diameter and blood flow velocity, and if we could detect cerebrovascular alterations after SAH and their impact on cerebral ischaemia. SAH was induced in 15 Wistar rats by means of the endovascular filament method; 6 other rats served as contro...
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Veröffentlicht in: | Acta neurochirurgica 2005-09, Vol.147 (9), p.977-983 |
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creator | van den Bergh, W M Schepers, J Veldhuis, W B Nicolay, K Tulleken, C A F Rinkel, G J E |
description | We developed an MRI protocol to measure cerebrovascular diameter and blood flow velocity, and if we could detect cerebrovascular alterations after SAH and their impact on cerebral ischaemia.
SAH was induced in 15 Wistar rats by means of the endovascular filament method; 6 other rats served as control. MRI measurements were performed on a 4.7T NMR spectrometer 1 and 48 hours after SAH and 9 days thereafter. Diffusion-weighted and T2-weighted images were acquired to detect cerebral ischaemia. The arterial spin labelling method was used to measure CBF. MR angiography was used to measure vessel diameter and blood flow velocity, from which the arterial blood flow was calculated.
The ischemic lesion volume increased between 1 and 48 hours after SAH from 0.039 to 0.26 ml (P = 0.003). CBF decreased from 53.6 to 39.1 ml/100 g/min. The vessel diameter had narrowed, the blood flow velocity diminished as did the arterial blood flow in most vessels, but only the vasoconstriction in the right proximal ICA reached significance (0.49 mm to 0.43 mm, P = 0.016). Baseline values were restored at day 9.
We showed that it is feasible to detect alterations of in-vivo vessel diameter and blood flow velocities and their consequences for brain damage after experimental SAH in the rat. The growth of the infarct volume between day 0 and 2 after SAH and the parallel vasoconstriction suggest that delayed cerebral ischaemia after SAH occurs in rats and that this may be caused by vasoconstriction. |
doi_str_mv | 10.1007/s00701-005-0539-x |
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SAH was induced in 15 Wistar rats by means of the endovascular filament method; 6 other rats served as control. MRI measurements were performed on a 4.7T NMR spectrometer 1 and 48 hours after SAH and 9 days thereafter. Diffusion-weighted and T2-weighted images were acquired to detect cerebral ischaemia. The arterial spin labelling method was used to measure CBF. MR angiography was used to measure vessel diameter and blood flow velocity, from which the arterial blood flow was calculated.
The ischemic lesion volume increased between 1 and 48 hours after SAH from 0.039 to 0.26 ml (P = 0.003). CBF decreased from 53.6 to 39.1 ml/100 g/min. The vessel diameter had narrowed, the blood flow velocity diminished as did the arterial blood flow in most vessels, but only the vasoconstriction in the right proximal ICA reached significance (0.49 mm to 0.43 mm, P = 0.016). Baseline values were restored at day 9.
We showed that it is feasible to detect alterations of in-vivo vessel diameter and blood flow velocities and their consequences for brain damage after experimental SAH in the rat. The growth of the infarct volume between day 0 and 2 after SAH and the parallel vasoconstriction suggest that delayed cerebral ischaemia after SAH occurs in rats and that this may be caused by vasoconstriction.</description><identifier>ISSN: 0001-6268</identifier><identifier>EISSN: 0942-0940</identifier><identifier>DOI: 10.1007/s00701-005-0539-x</identifier><identifier>PMID: 15900401</identifier><language>eng</language><publisher>Austria: Springer Nature B.V</publisher><subject>Animals ; Brain - blood supply ; Brain - pathology ; Brain - physiopathology ; Brain Infarction - etiology ; Brain Infarction - pathology ; Brain Infarction - physiopathology ; Brain Ischemia - etiology ; Brain Ischemia - pathology ; Brain Ischemia - physiopathology ; Cerebral Arteries - pathology ; Cerebral Arteries - physiopathology ; Cerebrovascular Circulation - physiology ; Circulatory system ; Disease Models, Animal ; Magnetic Resonance Angiography - methods ; Magnetic Resonance Imaging - methods ; Male ; Medical imaging ; Rats ; Rats, Wistar ; Rodents ; Subarachnoid Hemorrhage - complications ; Subarachnoid Hemorrhage - pathology ; Subarachnoid Hemorrhage - physiopathology ; Vasoconstriction - physiology ; Vasospasm, Intracranial - etiology ; Vasospasm, Intracranial - pathology ; Vasospasm, Intracranial - physiopathology</subject><ispartof>Acta neurochirurgica, 2005-09, Vol.147 (9), p.977-983</ispartof><rights>Springer-Verlag/Wien 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-e8dfbd3038f747d35d32b5db5da185960f77af8b80ad5e9e8902f4fe286709213</citedby><cites>FETCH-LOGICAL-c358t-e8dfbd3038f747d35d32b5db5da185960f77af8b80ad5e9e8902f4fe286709213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15900401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van den Bergh, W M</creatorcontrib><creatorcontrib>Schepers, J</creatorcontrib><creatorcontrib>Veldhuis, W B</creatorcontrib><creatorcontrib>Nicolay, K</creatorcontrib><creatorcontrib>Tulleken, C A F</creatorcontrib><creatorcontrib>Rinkel, G J E</creatorcontrib><title>Magnetic resonance imaging in experimental subarachnoid haemorrhage</title><title>Acta neurochirurgica</title><addtitle>Acta Neurochir (Wien)</addtitle><description>We developed an MRI protocol to measure cerebrovascular diameter and blood flow velocity, and if we could detect cerebrovascular alterations after SAH and their impact on cerebral ischaemia.
SAH was induced in 15 Wistar rats by means of the endovascular filament method; 6 other rats served as control. MRI measurements were performed on a 4.7T NMR spectrometer 1 and 48 hours after SAH and 9 days thereafter. Diffusion-weighted and T2-weighted images were acquired to detect cerebral ischaemia. The arterial spin labelling method was used to measure CBF. MR angiography was used to measure vessel diameter and blood flow velocity, from which the arterial blood flow was calculated.
The ischemic lesion volume increased between 1 and 48 hours after SAH from 0.039 to 0.26 ml (P = 0.003). CBF decreased from 53.6 to 39.1 ml/100 g/min. The vessel diameter had narrowed, the blood flow velocity diminished as did the arterial blood flow in most vessels, but only the vasoconstriction in the right proximal ICA reached significance (0.49 mm to 0.43 mm, P = 0.016). Baseline values were restored at day 9.
We showed that it is feasible to detect alterations of in-vivo vessel diameter and blood flow velocities and their consequences for brain damage after experimental SAH in the rat. The growth of the infarct volume between day 0 and 2 after SAH and the parallel vasoconstriction suggest that delayed cerebral ischaemia after SAH occurs in rats and that this may be caused by vasoconstriction.</description><subject>Animals</subject><subject>Brain - blood supply</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Brain Infarction - etiology</subject><subject>Brain Infarction - pathology</subject><subject>Brain Infarction - physiopathology</subject><subject>Brain Ischemia - etiology</subject><subject>Brain Ischemia - pathology</subject><subject>Brain Ischemia - physiopathology</subject><subject>Cerebral Arteries - pathology</subject><subject>Cerebral Arteries - physiopathology</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Circulatory system</subject><subject>Disease Models, Animal</subject><subject>Magnetic Resonance Angiography - methods</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Subarachnoid Hemorrhage - complications</subject><subject>Subarachnoid Hemorrhage - pathology</subject><subject>Subarachnoid Hemorrhage - physiopathology</subject><subject>Vasoconstriction - physiology</subject><subject>Vasospasm, Intracranial - etiology</subject><subject>Vasospasm, Intracranial - pathology</subject><subject>Vasospasm, Intracranial - physiopathology</subject><issn>0001-6268</issn><issn>0942-0940</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU9LxDAQxYMo7rr6AbxI8aCn6iRp2uQoi_9gxYueQ9pOul3adE22sH57s-yC4EEYZhLyew8yj5BLCncUoLgPsQFNAUQKgqt0e0SmoDKWxgbH8QzxNWe5nJCzEFbxxoqMn5IJFQogAzol8zfTONy0VeIxDM64CpO2N03rmqR1CW7X6Nse3cZ0SRhL4021dENbJ0uD_eD90jR4Tk6s6QJeHOaMfD49fsxf0sX78-v8YZFWXMhNirK2Zc2BS1tkRc1FzVkp6liGSqFysEVhrCwlmFqgQqmA2cwik3kBilE-I7d737UfvkYMG923ocKuMw6HMehCZELkkueRvPmXzKXgDHIVwes_4GoYvYu_2LkpJZWECNE9VPkhBI9Wr-NOjP_WFPQuCL0PQscg9C4IvY2aq4PxWPZY_yoOm-c_MiqDMA</recordid><startdate>200509</startdate><enddate>200509</enddate><creator>van den Bergh, W M</creator><creator>Schepers, J</creator><creator>Veldhuis, W B</creator><creator>Nicolay, K</creator><creator>Tulleken, C A F</creator><creator>Rinkel, G J E</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200509</creationdate><title>Magnetic resonance imaging in experimental subarachnoid haemorrhage</title><author>van den Bergh, W M ; Schepers, J ; Veldhuis, W B ; Nicolay, K ; Tulleken, C A F ; Rinkel, G J E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-e8dfbd3038f747d35d32b5db5da185960f77af8b80ad5e9e8902f4fe286709213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Brain - blood supply</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Brain Infarction - etiology</topic><topic>Brain Infarction - pathology</topic><topic>Brain Infarction - physiopathology</topic><topic>Brain Ischemia - etiology</topic><topic>Brain Ischemia - pathology</topic><topic>Brain Ischemia - physiopathology</topic><topic>Cerebral Arteries - pathology</topic><topic>Cerebral Arteries - physiopathology</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Circulatory system</topic><topic>Disease Models, Animal</topic><topic>Magnetic Resonance Angiography - methods</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rodents</topic><topic>Subarachnoid Hemorrhage - complications</topic><topic>Subarachnoid Hemorrhage - pathology</topic><topic>Subarachnoid Hemorrhage - physiopathology</topic><topic>Vasoconstriction - physiology</topic><topic>Vasospasm, Intracranial - etiology</topic><topic>Vasospasm, Intracranial - pathology</topic><topic>Vasospasm, Intracranial - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van den Bergh, W M</creatorcontrib><creatorcontrib>Schepers, J</creatorcontrib><creatorcontrib>Veldhuis, W B</creatorcontrib><creatorcontrib>Nicolay, K</creatorcontrib><creatorcontrib>Tulleken, C A F</creatorcontrib><creatorcontrib>Rinkel, G J E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neurochirurgica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van den Bergh, W M</au><au>Schepers, J</au><au>Veldhuis, W B</au><au>Nicolay, K</au><au>Tulleken, C A F</au><au>Rinkel, G J E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetic resonance imaging in experimental subarachnoid haemorrhage</atitle><jtitle>Acta neurochirurgica</jtitle><addtitle>Acta Neurochir (Wien)</addtitle><date>2005-09</date><risdate>2005</risdate><volume>147</volume><issue>9</issue><spage>977</spage><epage>983</epage><pages>977-983</pages><issn>0001-6268</issn><eissn>0942-0940</eissn><abstract>We developed an MRI protocol to measure cerebrovascular diameter and blood flow velocity, and if we could detect cerebrovascular alterations after SAH and their impact on cerebral ischaemia.
SAH was induced in 15 Wistar rats by means of the endovascular filament method; 6 other rats served as control. MRI measurements were performed on a 4.7T NMR spectrometer 1 and 48 hours after SAH and 9 days thereafter. Diffusion-weighted and T2-weighted images were acquired to detect cerebral ischaemia. The arterial spin labelling method was used to measure CBF. MR angiography was used to measure vessel diameter and blood flow velocity, from which the arterial blood flow was calculated.
The ischemic lesion volume increased between 1 and 48 hours after SAH from 0.039 to 0.26 ml (P = 0.003). CBF decreased from 53.6 to 39.1 ml/100 g/min. The vessel diameter had narrowed, the blood flow velocity diminished as did the arterial blood flow in most vessels, but only the vasoconstriction in the right proximal ICA reached significance (0.49 mm to 0.43 mm, P = 0.016). Baseline values were restored at day 9.
We showed that it is feasible to detect alterations of in-vivo vessel diameter and blood flow velocities and their consequences for brain damage after experimental SAH in the rat. The growth of the infarct volume between day 0 and 2 after SAH and the parallel vasoconstriction suggest that delayed cerebral ischaemia after SAH occurs in rats and that this may be caused by vasoconstriction.</abstract><cop>Austria</cop><pub>Springer Nature B.V</pub><pmid>15900401</pmid><doi>10.1007/s00701-005-0539-x</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Brain - blood supply Brain - pathology Brain - physiopathology Brain Infarction - etiology Brain Infarction - pathology Brain Infarction - physiopathology Brain Ischemia - etiology Brain Ischemia - pathology Brain Ischemia - physiopathology Cerebral Arteries - pathology Cerebral Arteries - physiopathology Cerebrovascular Circulation - physiology Circulatory system Disease Models, Animal Magnetic Resonance Angiography - methods Magnetic Resonance Imaging - methods Male Medical imaging Rats Rats, Wistar Rodents Subarachnoid Hemorrhage - complications Subarachnoid Hemorrhage - pathology Subarachnoid Hemorrhage - physiopathology Vasoconstriction - physiology Vasospasm, Intracranial - etiology Vasospasm, Intracranial - pathology Vasospasm, Intracranial - physiopathology |
title | Magnetic resonance imaging in experimental subarachnoid haemorrhage |
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