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Long-term changes of functional MRI-based brain function, behavioral status, and histopathology after transient focal cerebral ischemia in rats
The relation between recovery of brain function and neurological status after clinical and experimental cerebral ischemia is incompletely characterized. We assessed the evolution of ischemic injury, behavioral status, and brain activity at acute to chronic periods after transient middle cerebral art...
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Published in: | Stroke (1970) 2006-10, Vol.37 (10), p.2593-2600 |
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description | The relation between recovery of brain function and neurological status after clinical and experimental cerebral ischemia is incompletely characterized. We assessed the evolution of ischemic injury, behavioral status, and brain activity at acute to chronic periods after transient middle cerebral artery occlusion (tMCAO) in rats.
Male Sprague-Dawley rats were subjected to 20-minute tMCAO (n=10) or sham operation (n=10). Sensorimotor behavioral testing and multimodal (diffusion, perfusion, T2, and functional) MRI, as well as postmortem hematoxylin-eosin staining, were performed before and up to 21 days after tMCAO. MRI and histological parameters were evaluated in 5 regions of interest within the sensorimotor network. Diffusion, perfusion, and T2 lesion volumes were calculated according to previously established viability thresholds.
Diffusion and perfusion lesions were present during occlusion but disappeared completely and permanently within 30 minutes after reperfusion, with no T2 lesions seen. Functional MRI and behavioral deficits did not normalize until 1 and 21 days after tMCAO, respectively. Histology demonstrated selective neuronal cell death at 7 and 21 days after reperfusion.
Twenty-minute tMCAO produced distinct changes on multimodal MRI, histology, and behavioral parameters acutely and chronically. Normal findings on MRI after transient ischemia may not indicate normal tissue status, as behavioral and histological anomalies remain. Behavioral dysfunction persisting long after the recovery of MRI parameters may relate to the subtle neuronal damage seen on histology. Together, these results may help explain unremitting neurological deficits in stroke or transient ischemic attack patients with normal MRI findings. |
doi_str_mv | 10.1161/01.STR.0000239667.15532.c1 |
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Male Sprague-Dawley rats were subjected to 20-minute tMCAO (n=10) or sham operation (n=10). Sensorimotor behavioral testing and multimodal (diffusion, perfusion, T2, and functional) MRI, as well as postmortem hematoxylin-eosin staining, were performed before and up to 21 days after tMCAO. MRI and histological parameters were evaluated in 5 regions of interest within the sensorimotor network. Diffusion, perfusion, and T2 lesion volumes were calculated according to previously established viability thresholds.
Diffusion and perfusion lesions were present during occlusion but disappeared completely and permanently within 30 minutes after reperfusion, with no T2 lesions seen. Functional MRI and behavioral deficits did not normalize until 1 and 21 days after tMCAO, respectively. Histology demonstrated selective neuronal cell death at 7 and 21 days after reperfusion.
Twenty-minute tMCAO produced distinct changes on multimodal MRI, histology, and behavioral parameters acutely and chronically. Normal findings on MRI after transient ischemia may not indicate normal tissue status, as behavioral and histological anomalies remain. Behavioral dysfunction persisting long after the recovery of MRI parameters may relate to the subtle neuronal damage seen on histology. Together, these results may help explain unremitting neurological deficits in stroke or transient ischemic attack patients with normal MRI findings.</description><identifier>ISSN: 0039-2499</identifier><identifier>EISSN: 1524-4628</identifier><identifier>DOI: 10.1161/01.STR.0000239667.15532.c1</identifier><identifier>PMID: 16946164</identifier><identifier>CODEN: SJCCA7</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Animals ; Behavior, Animal ; Biological and medical sciences ; Brain - pathology ; Brain - physiopathology ; Brain Damage, Chronic - etiology ; Brain Damage, Chronic - pathology ; Brain Damage, Chronic - psychology ; Cell Death ; Diffusion Magnetic Resonance Imaging ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Hypercapnia - physiopathology ; Infarction, Middle Cerebral Artery - complications ; Infarction, Middle Cerebral Artery - pathology ; Infarction, Middle Cerebral Artery - physiopathology ; Infarction, Middle Cerebral Artery - psychology ; Ischemic Attack, Transient - complications ; Ischemic Attack, Transient - pathology ; Ischemic Attack, Transient - physiopathology ; Ischemic Attack, Transient - psychology ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Movement Disorders - etiology ; Movement Disorders - pathology ; Movement Disorders - physiopathology ; Nervous system (semeiology, syndromes) ; Neurology ; Neurons - pathology ; Neuropharmacology ; Neuroprotective agent ; Perceptual Disorders - etiology ; Perceptual Disorders - pathology ; Perceptual Disorders - physiopathology ; Pharmacology. Drug treatments ; Rats ; Rats, Sprague-Dawley ; Reaction Time ; Sensation Disorders - etiology ; Sensation Disorders - pathology ; Sensation Disorders - physiopathology ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Stroke (1970), 2006-10, Vol.37 (10), p.2593-2600</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-5dc95e0b471f39a73abc83c290d2943b48ef8648c3a1e8f764af32cd138470e13</citedby><cites>FETCH-LOGICAL-c588t-5dc95e0b471f39a73abc83c290d2943b48ef8648c3a1e8f764af32cd138470e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18169423$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16946164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SICARD, Kenneth M</creatorcontrib><creatorcontrib>HENNINGER, Nils</creatorcontrib><creatorcontrib>FISHER, Marc</creatorcontrib><creatorcontrib>DUONG, Timothy Q</creatorcontrib><creatorcontrib>FERRIS, Craig F</creatorcontrib><title>Long-term changes of functional MRI-based brain function, behavioral status, and histopathology after transient focal cerebral ischemia in rats</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>The relation between recovery of brain function and neurological status after clinical and experimental cerebral ischemia is incompletely characterized. We assessed the evolution of ischemic injury, behavioral status, and brain activity at acute to chronic periods after transient middle cerebral artery occlusion (tMCAO) in rats.
Male Sprague-Dawley rats were subjected to 20-minute tMCAO (n=10) or sham operation (n=10). Sensorimotor behavioral testing and multimodal (diffusion, perfusion, T2, and functional) MRI, as well as postmortem hematoxylin-eosin staining, were performed before and up to 21 days after tMCAO. MRI and histological parameters were evaluated in 5 regions of interest within the sensorimotor network. Diffusion, perfusion, and T2 lesion volumes were calculated according to previously established viability thresholds.
Diffusion and perfusion lesions were present during occlusion but disappeared completely and permanently within 30 minutes after reperfusion, with no T2 lesions seen. Functional MRI and behavioral deficits did not normalize until 1 and 21 days after tMCAO, respectively. Histology demonstrated selective neuronal cell death at 7 and 21 days after reperfusion.
Twenty-minute tMCAO produced distinct changes on multimodal MRI, histology, and behavioral parameters acutely and chronically. Normal findings on MRI after transient ischemia may not indicate normal tissue status, as behavioral and histological anomalies remain. Behavioral dysfunction persisting long after the recovery of MRI parameters may relate to the subtle neuronal damage seen on histology. Together, these results may help explain unremitting neurological deficits in stroke or transient ischemic attack patients with normal MRI findings.</description><subject>Animals</subject><subject>Behavior, Animal</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Brain Damage, Chronic - etiology</subject><subject>Brain Damage, Chronic - pathology</subject><subject>Brain Damage, Chronic - psychology</subject><subject>Cell Death</subject><subject>Diffusion Magnetic Resonance Imaging</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Hypercapnia - physiopathology</subject><subject>Infarction, Middle Cerebral Artery - complications</subject><subject>Infarction, Middle Cerebral Artery - pathology</subject><subject>Infarction, Middle Cerebral Artery - physiopathology</subject><subject>Infarction, Middle Cerebral Artery - psychology</subject><subject>Ischemic Attack, Transient - complications</subject><subject>Ischemic Attack, Transient - pathology</subject><subject>Ischemic Attack, Transient - physiopathology</subject><subject>Ischemic Attack, Transient - psychology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Movement Disorders - etiology</subject><subject>Movement Disorders - pathology</subject><subject>Movement Disorders - physiopathology</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Neuropharmacology</subject><subject>Neuroprotective agent</subject><subject>Perceptual Disorders - etiology</subject><subject>Perceptual Disorders - pathology</subject><subject>Perceptual Disorders - physiopathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reaction Time</subject><subject>Sensation Disorders - etiology</subject><subject>Sensation Disorders - pathology</subject><subject>Sensation Disorders - physiopathology</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0039-2499</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAURiMEokPhFZCFBKsmxD9xbBZIqCpQaRBSKWvrxrEnRkk82E6lPgWvXKcddWCFN17ccz99V6co3uC6wpjj9zWuflxfVXV-hErO2wo3DSWVxk-KDW4IKxkn4mmxqWsqS8KkPClexPjrnhfN8-IEc8k45mxT_Nn6eVcmEyakB5h3JiJvkV1mnZyfYUTfri7LDqLpURfAzY-jM9SZAW6cDxmKCdISzxDMPRpcTH4PafCj390isDkcpQBzdGZOyHqdF7QJpls3XdSDmRygHB0gxZfFMwtjNK8O_2nx8_PF9fnXcvv9y-X5p22pGyFS2fRaNqbuWIstldBS6LSgmsi6J5LRjgljBWdCU8BG2JYzsJToHlPB2tpgelp8fMjdL91kep2r5TpqH9wE4VZ5cOrfyewGtfM3KsdL2awB7w4Bwf9eTExqyreYcYTZ-CUqLoTklDT_BbGkHLeEZ_DDA6iDjzEY-9gG12oVr2qssnh1FK_uxSu91nn99z3H1YPpDLw9ABCzAZuFaBePnFhJQukdSTm7Fg</recordid><startdate>20061001</startdate><enddate>20061001</enddate><creator>SICARD, Kenneth M</creator><creator>HENNINGER, Nils</creator><creator>FISHER, Marc</creator><creator>DUONG, Timothy Q</creator><creator>FERRIS, Craig F</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20061001</creationdate><title>Long-term changes of functional MRI-based brain function, behavioral status, and histopathology after transient focal cerebral ischemia in rats</title><author>SICARD, Kenneth M ; HENNINGER, Nils ; FISHER, Marc ; DUONG, Timothy Q ; FERRIS, Craig F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-5dc95e0b471f39a73abc83c290d2943b48ef8648c3a1e8f764af32cd138470e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Behavior, Animal</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Brain Damage, Chronic - etiology</topic><topic>Brain Damage, Chronic - pathology</topic><topic>Brain Damage, Chronic - psychology</topic><topic>Cell Death</topic><topic>Diffusion Magnetic Resonance Imaging</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Hypercapnia - physiopathology</topic><topic>Infarction, Middle Cerebral Artery - complications</topic><topic>Infarction, Middle Cerebral Artery - pathology</topic><topic>Infarction, Middle Cerebral Artery - physiopathology</topic><topic>Infarction, Middle Cerebral Artery - psychology</topic><topic>Ischemic Attack, Transient - complications</topic><topic>Ischemic Attack, Transient - pathology</topic><topic>Ischemic Attack, Transient - physiopathology</topic><topic>Ischemic Attack, Transient - psychology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Movement Disorders - etiology</topic><topic>Movement Disorders - pathology</topic><topic>Movement Disorders - physiopathology</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Neuropharmacology</topic><topic>Neuroprotective agent</topic><topic>Perceptual Disorders - etiology</topic><topic>Perceptual Disorders - pathology</topic><topic>Perceptual Disorders - physiopathology</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reaction Time</topic><topic>Sensation Disorders - etiology</topic><topic>Sensation Disorders - pathology</topic><topic>Sensation Disorders - physiopathology</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SICARD, Kenneth M</creatorcontrib><creatorcontrib>HENNINGER, Nils</creatorcontrib><creatorcontrib>FISHER, Marc</creatorcontrib><creatorcontrib>DUONG, Timothy Q</creatorcontrib><creatorcontrib>FERRIS, Craig F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SICARD, Kenneth M</au><au>HENNINGER, Nils</au><au>FISHER, Marc</au><au>DUONG, Timothy Q</au><au>FERRIS, Craig F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term changes of functional MRI-based brain function, behavioral status, and histopathology after transient focal cerebral ischemia in rats</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2006-10-01</date><risdate>2006</risdate><volume>37</volume><issue>10</issue><spage>2593</spage><epage>2600</epage><pages>2593-2600</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>The relation between recovery of brain function and neurological status after clinical and experimental cerebral ischemia is incompletely characterized. We assessed the evolution of ischemic injury, behavioral status, and brain activity at acute to chronic periods after transient middle cerebral artery occlusion (tMCAO) in rats.
Male Sprague-Dawley rats were subjected to 20-minute tMCAO (n=10) or sham operation (n=10). Sensorimotor behavioral testing and multimodal (diffusion, perfusion, T2, and functional) MRI, as well as postmortem hematoxylin-eosin staining, were performed before and up to 21 days after tMCAO. MRI and histological parameters were evaluated in 5 regions of interest within the sensorimotor network. Diffusion, perfusion, and T2 lesion volumes were calculated according to previously established viability thresholds.
Diffusion and perfusion lesions were present during occlusion but disappeared completely and permanently within 30 minutes after reperfusion, with no T2 lesions seen. Functional MRI and behavioral deficits did not normalize until 1 and 21 days after tMCAO, respectively. Histology demonstrated selective neuronal cell death at 7 and 21 days after reperfusion.
Twenty-minute tMCAO produced distinct changes on multimodal MRI, histology, and behavioral parameters acutely and chronically. Normal findings on MRI after transient ischemia may not indicate normal tissue status, as behavioral and histological anomalies remain. Behavioral dysfunction persisting long after the recovery of MRI parameters may relate to the subtle neuronal damage seen on histology. Together, these results may help explain unremitting neurological deficits in stroke or transient ischemic attack patients with normal MRI findings.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>16946164</pmid><doi>10.1161/01.STR.0000239667.15532.c1</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Behavior, Animal Biological and medical sciences Brain - pathology Brain - physiopathology Brain Damage, Chronic - etiology Brain Damage, Chronic - pathology Brain Damage, Chronic - psychology Cell Death Diffusion Magnetic Resonance Imaging Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Hypercapnia - physiopathology Infarction, Middle Cerebral Artery - complications Infarction, Middle Cerebral Artery - pathology Infarction, Middle Cerebral Artery - physiopathology Infarction, Middle Cerebral Artery - psychology Ischemic Attack, Transient - complications Ischemic Attack, Transient - pathology Ischemic Attack, Transient - physiopathology Ischemic Attack, Transient - psychology Magnetic Resonance Imaging Male Medical sciences Movement Disorders - etiology Movement Disorders - pathology Movement Disorders - physiopathology Nervous system (semeiology, syndromes) Neurology Neurons - pathology Neuropharmacology Neuroprotective agent Perceptual Disorders - etiology Perceptual Disorders - pathology Perceptual Disorders - physiopathology Pharmacology. Drug treatments Rats Rats, Sprague-Dawley Reaction Time Sensation Disorders - etiology Sensation Disorders - pathology Sensation Disorders - physiopathology Vascular diseases and vascular malformations of the nervous system |
title | Long-term changes of functional MRI-based brain function, behavioral status, and histopathology after transient focal cerebral ischemia in rats |
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