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Temporary focal ischemia in the mouse: Technical aspects and patterns of Fluoro-Jade evident neurodegeneration
Animal models of cerebral infarction are crucial to understanding the mechanisms of neuronal survival following ischemic brain injury and to the development of therapeutic interventions for victims of all types of stroke. Rodents have been used extensively in such research. One rodent model of strok...
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Published in: | Brain research 2005-04, Vol.1042 (1), p.29-36 |
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description | Animal models of cerebral infarction are crucial to understanding the mechanisms of neuronal survival following ischemic brain injury and to the development of therapeutic interventions for victims of all types of stroke. Rodents have been used extensively in such research. One rodent model of stroke utilizes either permanent or temporary occlusion of the middle cerebral artery (MCAO) to produce ischemia. Since the development of an endovascular method for this was published in 1989, MCAO has been applied commonly to the rat, and often paired with 2, 3, 5-triphenyltetrazolium chloride (TTC) staining for stroke volume measurement. Meanwhile, advances in the ability to genetically alter mice have allowed exciting lines of research into ischemia. Because of technical demands and issues with survival, relatively few laboratories have investigated the MCAO method in the mouse. Our present work utilizes a mouse middle cerebral occlusion (MCAO) model of embolic stroke to study neuronal degeneration following temporary focal cerebral ischemia. C57Bl/6J mice were used to examine the exact effects of MCAO using Fluoro-Jade, a marker of neurodegeneration that allows observation of specific brain regions and cells destined to die. A time course of escalating neuronal degeneration from 10 min to 7 days following MCAO was established. Technical aspects of this popular method for transient focal ischemia as it applies to the mouse are discussed. |
doi_str_mv | 10.1016/j.brainres.2005.02.021 |
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Rodents have been used extensively in such research. One rodent model of stroke utilizes either permanent or temporary occlusion of the middle cerebral artery (MCAO) to produce ischemia. Since the development of an endovascular method for this was published in 1989, MCAO has been applied commonly to the rat, and often paired with 2, 3, 5-triphenyltetrazolium chloride (TTC) staining for stroke volume measurement. Meanwhile, advances in the ability to genetically alter mice have allowed exciting lines of research into ischemia. Because of technical demands and issues with survival, relatively few laboratories have investigated the MCAO method in the mouse. Our present work utilizes a mouse middle cerebral occlusion (MCAO) model of embolic stroke to study neuronal degeneration following temporary focal cerebral ischemia. C57Bl/6J mice were used to examine the exact effects of MCAO using Fluoro-Jade, a marker of neurodegeneration that allows observation of specific brain regions and cells destined to die. A time course of escalating neuronal degeneration from 10 min to 7 days following MCAO was established. Technical aspects of this popular method for transient focal ischemia as it applies to the mouse are discussed.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2005.02.021</identifier><identifier>PMID: 15823250</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Biomarkers - analysis ; Brain - cytology ; Brain - pathology ; Brain Injuries - pathology ; Cell Death ; Cerebral Cortex - cytology ; Cerebral Cortex - pathology ; Corpus Striatum - cytology ; Corpus Striatum - pathology ; Disease Models, Animal ; Fluoresceins ; Fluorescent Dyes - analysis ; Fluoro-Jade ; Focal ischemia ; Hippocampus - cytology ; Hippocampus - pathology ; Infarction, Middle Cerebral Artery - pathology ; Ischemic Attack, Transient - pathology ; MCAO ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mouse ; Nerve Degeneration - pathology ; Neurodegeneration ; Neurology ; Neurons - pathology ; Organic Chemicals ; Staining and Labeling - methods ; Tetrazolium Salts - analysis ; Time Factors ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Brain research, 2005-04, Vol.1042 (1), p.29-36</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-3ed77f880ebfbe2917ca4b9d96c9b1217a56789dc6b9127bf68dde85d02288b63</citedby><cites>FETCH-LOGICAL-c524t-3ed77f880ebfbe2917ca4b9d96c9b1217a56789dc6b9127bf68dde85d02288b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16714029$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15823250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duckworth, Edward A.M.</creatorcontrib><creatorcontrib>Butler, Tanya L.</creatorcontrib><creatorcontrib>De Mesquita, Dirson</creatorcontrib><creatorcontrib>Collier, Shane N.</creatorcontrib><creatorcontrib>Collier, Lisa</creatorcontrib><creatorcontrib>Pennypacker, Keith R.</creatorcontrib><title>Temporary focal ischemia in the mouse: Technical aspects and patterns of Fluoro-Jade evident neurodegeneration</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Animal models of cerebral infarction are crucial to understanding the mechanisms of neuronal survival following ischemic brain injury and to the development of therapeutic interventions for victims of all types of stroke. Rodents have been used extensively in such research. One rodent model of stroke utilizes either permanent or temporary occlusion of the middle cerebral artery (MCAO) to produce ischemia. Since the development of an endovascular method for this was published in 1989, MCAO has been applied commonly to the rat, and often paired with 2, 3, 5-triphenyltetrazolium chloride (TTC) staining for stroke volume measurement. Meanwhile, advances in the ability to genetically alter mice have allowed exciting lines of research into ischemia. Because of technical demands and issues with survival, relatively few laboratories have investigated the MCAO method in the mouse. Our present work utilizes a mouse middle cerebral occlusion (MCAO) model of embolic stroke to study neuronal degeneration following temporary focal cerebral ischemia. C57Bl/6J mice were used to examine the exact effects of MCAO using Fluoro-Jade, a marker of neurodegeneration that allows observation of specific brain regions and cells destined to die. A time course of escalating neuronal degeneration from 10 min to 7 days following MCAO was established. Technical aspects of this popular method for transient focal ischemia as it applies to the mouse are discussed.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Brain - cytology</subject><subject>Brain - pathology</subject><subject>Brain Injuries - pathology</subject><subject>Cell Death</subject><subject>Cerebral Cortex - cytology</subject><subject>Cerebral Cortex - pathology</subject><subject>Corpus Striatum - cytology</subject><subject>Corpus Striatum - pathology</subject><subject>Disease Models, Animal</subject><subject>Fluoresceins</subject><subject>Fluorescent Dyes - analysis</subject><subject>Fluoro-Jade</subject><subject>Focal ischemia</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - pathology</subject><subject>Infarction, Middle Cerebral Artery - pathology</subject><subject>Ischemic Attack, Transient - pathology</subject><subject>MCAO</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mouse</subject><subject>Nerve Degeneration - pathology</subject><subject>Neurodegeneration</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Organic Chemicals</subject><subject>Staining and Labeling - methods</subject><subject>Tetrazolium Salts - analysis</subject><subject>Time Factors</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQQCMEotvCX6h8gVsWe5L4gxOoohRUictythx7wnqV2MFOKvXf49Uu6nGlkUaW3oxn5lXVLaNbRhn_dNj2yfiQMG-B0m5LoQR7VW2YFFBzaOnrakMp5bVUqrmqrnM-lGfTKPq2umKdhAY6uqnCDqc5JpOeyRCtGYnPdo-TN8QHsuyRTHHN-Jns0O6DPwImz2iXTExwZDbLgilkEgdyP64xxfqncUjwyTsMCwm4pujwDwZMZvExvKveDGbM-P6cb6rf9992dw_146_vP-6-Pta2g3apG3RCDFJS7IceQTFhTdsrp7hVPQMmTMeFVM7yXjEQ_cClcyg7RwGk7HlzU3089Z1T_LtiXvRUFsNxNAHLQpoLAZwBXASBCtYAvwwy0bSyAVFAfgJtijknHPSc_FQOrBnVR3f6oP-700d3mkIJVgpvzz-s_YTupewsqwAfzoDJxcSQTLA-v3BcsJaCKtyXE4flwk8ek87WY7DofCrqtIv-0iz_AHe5vDQ</recordid><startdate>20050425</startdate><enddate>20050425</enddate><creator>Duckworth, Edward A.M.</creator><creator>Butler, Tanya L.</creator><creator>De Mesquita, Dirson</creator><creator>Collier, Shane N.</creator><creator>Collier, Lisa</creator><creator>Pennypacker, Keith R.</creator><general>Elsevier B.V</general><general>Elsevier</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></search><sort><creationdate>20050425</creationdate><title>Temporary focal ischemia in the mouse: Technical aspects and patterns of Fluoro-Jade evident neurodegeneration</title><author>Duckworth, Edward A.M. ; Butler, Tanya L. ; De Mesquita, Dirson ; Collier, Shane N. ; Collier, Lisa ; Pennypacker, Keith R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-3ed77f880ebfbe2917ca4b9d96c9b1217a56789dc6b9127bf68dde85d02288b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Brain - cytology</topic><topic>Brain - pathology</topic><topic>Brain Injuries - pathology</topic><topic>Cell Death</topic><topic>Cerebral Cortex - cytology</topic><topic>Cerebral Cortex - pathology</topic><topic>Corpus Striatum - cytology</topic><topic>Corpus Striatum - pathology</topic><topic>Disease Models, Animal</topic><topic>Fluoresceins</topic><topic>Fluorescent Dyes - analysis</topic><topic>Fluoro-Jade</topic><topic>Focal ischemia</topic><topic>Hippocampus - cytology</topic><topic>Hippocampus - pathology</topic><topic>Infarction, Middle Cerebral Artery - pathology</topic><topic>Ischemic Attack, Transient - pathology</topic><topic>MCAO</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mouse</topic><topic>Nerve Degeneration - pathology</topic><topic>Neurodegeneration</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Organic Chemicals</topic><topic>Staining and Labeling - methods</topic><topic>Tetrazolium Salts - analysis</topic><topic>Time Factors</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duckworth, Edward A.M.</creatorcontrib><creatorcontrib>Butler, Tanya L.</creatorcontrib><creatorcontrib>De Mesquita, Dirson</creatorcontrib><creatorcontrib>Collier, Shane N.</creatorcontrib><creatorcontrib>Collier, Lisa</creatorcontrib><creatorcontrib>Pennypacker, Keith R.</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><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duckworth, Edward A.M.</au><au>Butler, Tanya L.</au><au>De Mesquita, Dirson</au><au>Collier, Shane N.</au><au>Collier, Lisa</au><au>Pennypacker, Keith R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporary focal ischemia in the mouse: Technical aspects and patterns of Fluoro-Jade evident neurodegeneration</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2005-04-25</date><risdate>2005</risdate><volume>1042</volume><issue>1</issue><spage>29</spage><epage>36</epage><pages>29-36</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Animal models of cerebral infarction are crucial to understanding the mechanisms of neuronal survival following ischemic brain injury and to the development of therapeutic interventions for victims of all types of stroke. Rodents have been used extensively in such research. One rodent model of stroke utilizes either permanent or temporary occlusion of the middle cerebral artery (MCAO) to produce ischemia. Since the development of an endovascular method for this was published in 1989, MCAO has been applied commonly to the rat, and often paired with 2, 3, 5-triphenyltetrazolium chloride (TTC) staining for stroke volume measurement. Meanwhile, advances in the ability to genetically alter mice have allowed exciting lines of research into ischemia. Because of technical demands and issues with survival, relatively few laboratories have investigated the MCAO method in the mouse. Our present work utilizes a mouse middle cerebral occlusion (MCAO) model of embolic stroke to study neuronal degeneration following temporary focal cerebral ischemia. C57Bl/6J mice were used to examine the exact effects of MCAO using Fluoro-Jade, a marker of neurodegeneration that allows observation of specific brain regions and cells destined to die. A time course of escalating neuronal degeneration from 10 min to 7 days following MCAO was established. Technical aspects of this popular method for transient focal ischemia as it applies to the mouse are discussed.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>15823250</pmid><doi>10.1016/j.brainres.2005.02.021</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Biomarkers - analysis Brain - cytology Brain - pathology Brain Injuries - pathology Cell Death Cerebral Cortex - cytology Cerebral Cortex - pathology Corpus Striatum - cytology Corpus Striatum - pathology Disease Models, Animal Fluoresceins Fluorescent Dyes - analysis Fluoro-Jade Focal ischemia Hippocampus - cytology Hippocampus - pathology Infarction, Middle Cerebral Artery - pathology Ischemic Attack, Transient - pathology MCAO Medical sciences Mice Mice, Inbred C57BL Mouse Nerve Degeneration - pathology Neurodegeneration Neurology Neurons - pathology Organic Chemicals Staining and Labeling - methods Tetrazolium Salts - analysis Time Factors Vascular diseases and vascular malformations of the nervous system |
title | Temporary focal ischemia in the mouse: Technical aspects and patterns of Fluoro-Jade evident neurodegeneration |
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