Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat
Functional magnetic resonance imaging (fMRI) techniques highlight cerebral vascular responses which are coupled to changes in neural activation. However, two major difficulties arise when employing these techniques in animal studies. First is the disturbance of cerebral blood flow due to anaesthesia...
Gespeichert in:
Veröffentlicht in: | NeuroImage (Orlando, Fla.) Fla.), 2010-07, Vol.51 (4), p.1395-1404 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1404 |
---|---|
container_issue | 4 |
container_start_page | 1395 |
container_title | NeuroImage (Orlando, Fla.) |
container_volume | 51 |
creator | Griffin, Karen M. Blau, Christoph W. Kelly, Michael E. O'Herlihy, Colm O'Connell, P.R. Jones, James F.X. Kerskens, Christian M. |
description | Functional magnetic resonance imaging (fMRI) techniques highlight cerebral vascular responses which are coupled to changes in neural activation. However, two major difficulties arise when employing these techniques in animal studies. First is the disturbance of cerebral blood flow due to anaesthesia and second is the difficulty of precise reproducible quantitative measurements. These difficulties were surmounted in the current study by using propofol and quantitative arterial spin labelling (QASL) to measure relative cerebral blood volume of labelled water (rCBVlw), mean transit time (MTT) and capillary transit time (CTT). The ASL method was applied to measure the haemodynamic response in the primary somatosensory cortex following forepaw stimulation in the rat. Following stimulation an increase in signal intensity and rCBVlw was recorded, this was accompanied by a significant decrease in MTT (1.97±0.06s to 1.44±0.04s) and CTT (1.76±0.06s to 1.39±0.07s). Two animals were scanned repeatedly on two different experimental days. Stimulation in the first animal was applied to the same forepaw during the initial and repeat scan. In the second animal stimulation was applied to different forepaws on the first and second days. The control and activated ASL signal intensities, rCBVlw on both days were almost identical in both animals. The basal MTT and CTT during the second scan were also very similar to the values obtained during the first scan. The MTT recorded from the animal that underwent stimulation to the same paw during both scanning sessions was very similar on the first and second days. In conclusion, propofol induces little physiological disturbance and holds potential for longitudinal QASL fMRI studies. |
doi_str_mv | 10.1016/j.neuroimage.2010.03.024 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_745729267</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1053811910002946</els_id><sourcerecordid>3244847131</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-174b87e94037b6b8011bad1797dda125ddc6b9819383fcb2972aa4ad76cd47193</originalsourceid><addsrcrecordid>eNqFkUtv1TAQhSMEoi_-ArLEglUu40diewkVL6lSu6Bry7EnxVe5cWo7rfj3OLoFJDZd2Zr5xnN8TtMQCjsKtP-w3824phgO9g53DGoZ-A6YeNGcUtBdqzvJXm73jreKUn3SnOW8BwBNhXrdnDDgIEB2p83hJsUljnEidpriYyZLQhcykvvVziUUW8IDEpsKpmAnkpcwk8kOOE1hviPjOrsS4lw7VcqMJTiSMNfC7JBs8jaqjpSfSJItF82r0U4Z3zyd583tl88_Lr-1V9dfv19-vGqdULy0VIpBSdQCuBz6QQGlg_VUaum9pazz3vWDVlRzxUc3MC2ZtcJ62TsvZC2fN--P7y4p3q-YizmE7KpoO2Ncs5GiGqRZL58nOe-YArGR7_4j93FN9evZ0A56xRX0rFLqSLkUc044miVVH9IvQ8Fs2Zm9-Zed2bIzwE3Nro6-fVqwDgf0fwf_hFWBT0cAq3UPAZPJLmB12ocaWjE-hue3_Abau7Dd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1506838062</pqid></control><display><type>article</type><title>Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Griffin, Karen M. ; Blau, Christoph W. ; Kelly, Michael E. ; O'Herlihy, Colm ; O'Connell, P.R. ; Jones, James F.X. ; Kerskens, Christian M.</creator><creatorcontrib>Griffin, Karen M. ; Blau, Christoph W. ; Kelly, Michael E. ; O'Herlihy, Colm ; O'Connell, P.R. ; Jones, James F.X. ; Kerskens, Christian M.</creatorcontrib><description>Functional magnetic resonance imaging (fMRI) techniques highlight cerebral vascular responses which are coupled to changes in neural activation. However, two major difficulties arise when employing these techniques in animal studies. First is the disturbance of cerebral blood flow due to anaesthesia and second is the difficulty of precise reproducible quantitative measurements. These difficulties were surmounted in the current study by using propofol and quantitative arterial spin labelling (QASL) to measure relative cerebral blood volume of labelled water (rCBVlw), mean transit time (MTT) and capillary transit time (CTT). The ASL method was applied to measure the haemodynamic response in the primary somatosensory cortex following forepaw stimulation in the rat. Following stimulation an increase in signal intensity and rCBVlw was recorded, this was accompanied by a significant decrease in MTT (1.97±0.06s to 1.44±0.04s) and CTT (1.76±0.06s to 1.39±0.07s). Two animals were scanned repeatedly on two different experimental days. Stimulation in the first animal was applied to the same forepaw during the initial and repeat scan. In the second animal stimulation was applied to different forepaws on the first and second days. The control and activated ASL signal intensities, rCBVlw on both days were almost identical in both animals. The basal MTT and CTT during the second scan were also very similar to the values obtained during the first scan. The MTT recorded from the animal that underwent stimulation to the same paw during both scanning sessions was very similar on the first and second days. In conclusion, propofol induces little physiological disturbance and holds potential for longitudinal QASL fMRI studies.</description><identifier>ISSN: 1053-8119</identifier><identifier>EISSN: 1095-9572</identifier><identifier>DOI: 10.1016/j.neuroimage.2010.03.024</identifier><identifier>PMID: 20304075</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Action Potentials - physiology ; Anesthetics, Intravenous - pharmacology ; Animals ; Arterial spin labelling ; Arteries - anatomy & histology ; Blood oxygenation level dependent ; Blood Volume - drug effects ; Brachial Plexus - drug effects ; Brain ; Capillaries - drug effects ; Cerebrovascular Circulation - drug effects ; Electrophysiology ; Female ; Forepaw stimulation ; Functional magnetic resonance imaging ; Heart Rate - drug effects ; Heart Rate - physiology ; Labeling ; Magnetic Resonance Imaging - methods ; Medical research ; Methods ; NMR ; Nuclear magnetic resonance ; Oxygen - blood ; Propofol ; Propofol - pharmacology ; Rats ; Rats, Wistar ; Reproducibility of Results ; Respiratory Mechanics - drug effects ; Respiratory Mechanics - physiology ; Somatosensory cortex ; Somatosensory Cortex - anatomy & histology ; Somatosensory Cortex - blood supply ; Spin Labels ; Studies</subject><ispartof>NeuroImage (Orlando, Fla.), 2010-07, Vol.51 (4), p.1395-1404</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Jul 15, 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-174b87e94037b6b8011bad1797dda125ddc6b9819383fcb2972aa4ad76cd47193</citedby><cites>FETCH-LOGICAL-c483t-174b87e94037b6b8011bad1797dda125ddc6b9819383fcb2972aa4ad76cd47193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053811910002946$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20304075$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Griffin, Karen M.</creatorcontrib><creatorcontrib>Blau, Christoph W.</creatorcontrib><creatorcontrib>Kelly, Michael E.</creatorcontrib><creatorcontrib>O'Herlihy, Colm</creatorcontrib><creatorcontrib>O'Connell, P.R.</creatorcontrib><creatorcontrib>Jones, James F.X.</creatorcontrib><creatorcontrib>Kerskens, Christian M.</creatorcontrib><title>Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat</title><title>NeuroImage (Orlando, Fla.)</title><addtitle>Neuroimage</addtitle><description>Functional magnetic resonance imaging (fMRI) techniques highlight cerebral vascular responses which are coupled to changes in neural activation. However, two major difficulties arise when employing these techniques in animal studies. First is the disturbance of cerebral blood flow due to anaesthesia and second is the difficulty of precise reproducible quantitative measurements. These difficulties were surmounted in the current study by using propofol and quantitative arterial spin labelling (QASL) to measure relative cerebral blood volume of labelled water (rCBVlw), mean transit time (MTT) and capillary transit time (CTT). The ASL method was applied to measure the haemodynamic response in the primary somatosensory cortex following forepaw stimulation in the rat. Following stimulation an increase in signal intensity and rCBVlw was recorded, this was accompanied by a significant decrease in MTT (1.97±0.06s to 1.44±0.04s) and CTT (1.76±0.06s to 1.39±0.07s). Two animals were scanned repeatedly on two different experimental days. Stimulation in the first animal was applied to the same forepaw during the initial and repeat scan. In the second animal stimulation was applied to different forepaws on the first and second days. The control and activated ASL signal intensities, rCBVlw on both days were almost identical in both animals. The basal MTT and CTT during the second scan were also very similar to the values obtained during the first scan. The MTT recorded from the animal that underwent stimulation to the same paw during both scanning sessions was very similar on the first and second days. In conclusion, propofol induces little physiological disturbance and holds potential for longitudinal QASL fMRI studies.</description><subject>Action Potentials - physiology</subject><subject>Anesthetics, Intravenous - pharmacology</subject><subject>Animals</subject><subject>Arterial spin labelling</subject><subject>Arteries - anatomy & histology</subject><subject>Blood oxygenation level dependent</subject><subject>Blood Volume - drug effects</subject><subject>Brachial Plexus - drug effects</subject><subject>Brain</subject><subject>Capillaries - drug effects</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Electrophysiology</subject><subject>Female</subject><subject>Forepaw stimulation</subject><subject>Functional magnetic resonance imaging</subject><subject>Heart Rate - drug effects</subject><subject>Heart Rate - physiology</subject><subject>Labeling</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Medical research</subject><subject>Methods</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oxygen - blood</subject><subject>Propofol</subject><subject>Propofol - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reproducibility of Results</subject><subject>Respiratory Mechanics - drug effects</subject><subject>Respiratory Mechanics - physiology</subject><subject>Somatosensory cortex</subject><subject>Somatosensory Cortex - anatomy & histology</subject><subject>Somatosensory Cortex - blood supply</subject><subject>Spin Labels</subject><subject>Studies</subject><issn>1053-8119</issn><issn>1095-9572</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUtv1TAQhSMEoi_-ArLEglUu40diewkVL6lSu6Bry7EnxVe5cWo7rfj3OLoFJDZd2Zr5xnN8TtMQCjsKtP-w3824phgO9g53DGoZ-A6YeNGcUtBdqzvJXm73jreKUn3SnOW8BwBNhXrdnDDgIEB2p83hJsUljnEidpriYyZLQhcykvvVziUUW8IDEpsKpmAnkpcwk8kOOE1hviPjOrsS4lw7VcqMJTiSMNfC7JBs8jaqjpSfSJItF82r0U4Z3zyd583tl88_Lr-1V9dfv19-vGqdULy0VIpBSdQCuBz6QQGlg_VUaum9pazz3vWDVlRzxUc3MC2ZtcJ62TsvZC2fN--P7y4p3q-YizmE7KpoO2Ncs5GiGqRZL58nOe-YArGR7_4j93FN9evZ0A56xRX0rFLqSLkUc044miVVH9IvQ8Fs2Zm9-Zed2bIzwE3Nro6-fVqwDgf0fwf_hFWBT0cAq3UPAZPJLmB12ocaWjE-hue3_Abau7Dd</recordid><startdate>20100715</startdate><enddate>20100715</enddate><creator>Griffin, Karen M.</creator><creator>Blau, Christoph W.</creator><creator>Kelly, Michael E.</creator><creator>O'Herlihy, Colm</creator><creator>O'Connell, P.R.</creator><creator>Jones, James F.X.</creator><creator>Kerskens, Christian M.</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20100715</creationdate><title>Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat</title><author>Griffin, Karen M. ; Blau, Christoph W. ; Kelly, Michael E. ; O'Herlihy, Colm ; O'Connell, P.R. ; Jones, James F.X. ; Kerskens, Christian M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-174b87e94037b6b8011bad1797dda125ddc6b9819383fcb2972aa4ad76cd47193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Action Potentials - physiology</topic><topic>Anesthetics, Intravenous - pharmacology</topic><topic>Animals</topic><topic>Arterial spin labelling</topic><topic>Arteries - anatomy & histology</topic><topic>Blood oxygenation level dependent</topic><topic>Blood Volume - drug effects</topic><topic>Brachial Plexus - drug effects</topic><topic>Brain</topic><topic>Capillaries - drug effects</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Electrophysiology</topic><topic>Female</topic><topic>Forepaw stimulation</topic><topic>Functional magnetic resonance imaging</topic><topic>Heart Rate - drug effects</topic><topic>Heart Rate - physiology</topic><topic>Labeling</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Medical research</topic><topic>Methods</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Oxygen - blood</topic><topic>Propofol</topic><topic>Propofol - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reproducibility of Results</topic><topic>Respiratory Mechanics - drug effects</topic><topic>Respiratory Mechanics - physiology</topic><topic>Somatosensory cortex</topic><topic>Somatosensory Cortex - anatomy & histology</topic><topic>Somatosensory Cortex - blood supply</topic><topic>Spin Labels</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Griffin, Karen M.</creatorcontrib><creatorcontrib>Blau, Christoph W.</creatorcontrib><creatorcontrib>Kelly, Michael E.</creatorcontrib><creatorcontrib>O'Herlihy, Colm</creatorcontrib><creatorcontrib>O'Connell, P.R.</creatorcontrib><creatorcontrib>Jones, James F.X.</creatorcontrib><creatorcontrib>Kerskens, Christian M.</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>NeuroImage (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Griffin, Karen M.</au><au>Blau, Christoph W.</au><au>Kelly, Michael E.</au><au>O'Herlihy, Colm</au><au>O'Connell, P.R.</au><au>Jones, James F.X.</au><au>Kerskens, Christian M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat</atitle><jtitle>NeuroImage (Orlando, Fla.)</jtitle><addtitle>Neuroimage</addtitle><date>2010-07-15</date><risdate>2010</risdate><volume>51</volume><issue>4</issue><spage>1395</spage><epage>1404</epage><pages>1395-1404</pages><issn>1053-8119</issn><eissn>1095-9572</eissn><abstract>Functional magnetic resonance imaging (fMRI) techniques highlight cerebral vascular responses which are coupled to changes in neural activation. However, two major difficulties arise when employing these techniques in animal studies. First is the disturbance of cerebral blood flow due to anaesthesia and second is the difficulty of precise reproducible quantitative measurements. These difficulties were surmounted in the current study by using propofol and quantitative arterial spin labelling (QASL) to measure relative cerebral blood volume of labelled water (rCBVlw), mean transit time (MTT) and capillary transit time (CTT). The ASL method was applied to measure the haemodynamic response in the primary somatosensory cortex following forepaw stimulation in the rat. Following stimulation an increase in signal intensity and rCBVlw was recorded, this was accompanied by a significant decrease in MTT (1.97±0.06s to 1.44±0.04s) and CTT (1.76±0.06s to 1.39±0.07s). Two animals were scanned repeatedly on two different experimental days. Stimulation in the first animal was applied to the same forepaw during the initial and repeat scan. In the second animal stimulation was applied to different forepaws on the first and second days. The control and activated ASL signal intensities, rCBVlw on both days were almost identical in both animals. The basal MTT and CTT during the second scan were also very similar to the values obtained during the first scan. The MTT recorded from the animal that underwent stimulation to the same paw during both scanning sessions was very similar on the first and second days. In conclusion, propofol induces little physiological disturbance and holds potential for longitudinal QASL fMRI studies.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20304075</pmid><doi>10.1016/j.neuroimage.2010.03.024</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1053-8119 |
ispartof | NeuroImage (Orlando, Fla.), 2010-07, Vol.51 (4), p.1395-1404 |
issn | 1053-8119 1095-9572 |
language | eng |
recordid | cdi_proquest_miscellaneous_745729267 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Action Potentials - physiology Anesthetics, Intravenous - pharmacology Animals Arterial spin labelling Arteries - anatomy & histology Blood oxygenation level dependent Blood Volume - drug effects Brachial Plexus - drug effects Brain Capillaries - drug effects Cerebrovascular Circulation - drug effects Electrophysiology Female Forepaw stimulation Functional magnetic resonance imaging Heart Rate - drug effects Heart Rate - physiology Labeling Magnetic Resonance Imaging - methods Medical research Methods NMR Nuclear magnetic resonance Oxygen - blood Propofol Propofol - pharmacology Rats Rats, Wistar Reproducibility of Results Respiratory Mechanics - drug effects Respiratory Mechanics - physiology Somatosensory cortex Somatosensory Cortex - anatomy & histology Somatosensory Cortex - blood supply Spin Labels Studies |
title | Propofol allows precise quantitative arterial spin labelling functional magnetic resonance imaging in the rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T00%3A18%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Propofol%20allows%20precise%20quantitative%20arterial%20spin%20labelling%20functional%20magnetic%20resonance%20imaging%20in%20the%20rat&rft.jtitle=NeuroImage%20(Orlando,%20Fla.)&rft.au=Griffin,%20Karen%20M.&rft.date=2010-07-15&rft.volume=51&rft.issue=4&rft.spage=1395&rft.epage=1404&rft.pages=1395-1404&rft.issn=1053-8119&rft.eissn=1095-9572&rft_id=info:doi/10.1016/j.neuroimage.2010.03.024&rft_dat=%3Cproquest_cross%3E3244847131%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1506838062&rft_id=info:pmid/20304075&rft_els_id=S1053811910002946&rfr_iscdi=true |