Training the brain to survive stroke
Presently, little can be done to repair brain tissue after stroke damage. We hypothesized that the mammalian brain has an intrinsic capacity to adapt to low oxygen which would improve outcome from a reversible hypoxic/ischemic episode. Acclimation to chronic hypoxia causes increased capillarity and...
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description | Presently, little can be done to repair brain tissue after stroke damage. We hypothesized that the mammalian brain has an intrinsic capacity to adapt to low oxygen which would improve outcome from a reversible hypoxic/ischemic episode. Acclimation to chronic hypoxia causes increased capillarity and tissue oxygen levels which may improve the capacity to survive ischemia. Identification of these adaptations will lead to protocols which high risk groups could use to improve recovery and reduce costs.
Rats were exposed to hypoxia (3 weeks living at ½ an atmosphere). After acclimation, capillary density was measured morphometrically and was increased by 30% in the cortex. Novel implantable oxygen sensors showed that partial pressure of oxygen in the brain was increased by 40% in the normal cortex. Infarcts were induced in brain with 1 h reversible middle cerebral artery occlusions. After ischemia (48 h) behavioural scores were improved and T2 weighted MRI lesion volumes were reduced by 52% in acclimated groups. There was a reduction in inflammation indicated by reduced lymphocytes (by 27-33%), and ED1 positive cells (by 35-45%).
It is possible to stimulate a natural adaptive mechanism in the brain which will reduce damage and improve outcome for a given ischemic event. Since these adaptations occur after factors such as HIF-1α have returned to baseline, protection is likely related more to morphological changes such as angiogenesis. Such pre-conditioning, perhaps with exercise or pharmaceuticals, would not necessarily reduce the incidence of stroke, but the severity of damage could be reduced by 50%. |
doi_str_mv | 10.1371/journal.pone.0045108 |
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Rats were exposed to hypoxia (3 weeks living at ½ an atmosphere). After acclimation, capillary density was measured morphometrically and was increased by 30% in the cortex. Novel implantable oxygen sensors showed that partial pressure of oxygen in the brain was increased by 40% in the normal cortex. Infarcts were induced in brain with 1 h reversible middle cerebral artery occlusions. After ischemia (48 h) behavioural scores were improved and T2 weighted MRI lesion volumes were reduced by 52% in acclimated groups. There was a reduction in inflammation indicated by reduced lymphocytes (by 27-33%), and ED1 positive cells (by 35-45%).
It is possible to stimulate a natural adaptive mechanism in the brain which will reduce damage and improve outcome for a given ischemic event. Since these adaptations occur after factors such as HIF-1α have returned to baseline, protection is likely related more to morphological changes such as angiogenesis. Such pre-conditioning, perhaps with exercise or pharmaceuticals, would not necessarily reduce the incidence of stroke, but the severity of damage could be reduced by 50%.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0045108</identifier><identifier>PMID: 23028788</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acclimation ; Acclimatization ; Adaptation ; Angiogenesis ; Animals ; Biology ; Brain ; Brain - blood supply ; Brain - pathology ; Brain - physiopathology ; Brain damage ; Brain injury ; Capillarity ; Cerebral Infarction - pathology ; Cerebral Infarction - physiopathology ; Exercise ; Hypoxia ; Hypoxia, Brain - complications ; Hypoxia, Brain - physiopathology ; Ischemia ; Lymphocyte Count ; Lymphocytes ; Magnetic resonance imaging ; Male ; Medicine ; Neurosciences ; Occlusion ; Oxygen ; Oxygen - metabolism ; Oxygen probes ; Partial Pressure ; Physical fitness ; Physiology ; Preconditioning ; Rats ; Rats, Wistar ; Risk groups ; Rodents ; Sensors ; Stem cells ; Stroke ; Stroke - etiology ; Stroke - pathology ; Stroke - physiopathology ; Stroke - prevention & control ; Studies ; T-Lymphocytes - immunology ; Vascular endothelial growth factor</subject><ispartof>PloS one, 2012-09, Vol.7 (9), p.e45108-e45108</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Dunn et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Dunn et al 2012 Dunn et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-bafd3dbc14e73f9d09e6465ff1d0fb71b5d300901a6c660281df7eb5f5fba7a23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441606/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441606/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23028788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Baron, Jean-Claude</contributor><creatorcontrib>Dunn, Jeff F</creatorcontrib><creatorcontrib>Wu, Ying</creatorcontrib><creatorcontrib>Zhao, Zonghang</creatorcontrib><creatorcontrib>Srinivasan, Sathya</creatorcontrib><creatorcontrib>Natah, Sirajedin S</creatorcontrib><title>Training the brain to survive stroke</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Presently, little can be done to repair brain tissue after stroke damage. We hypothesized that the mammalian brain has an intrinsic capacity to adapt to low oxygen which would improve outcome from a reversible hypoxic/ischemic episode. Acclimation to chronic hypoxia causes increased capillarity and tissue oxygen levels which may improve the capacity to survive ischemia. Identification of these adaptations will lead to protocols which high risk groups could use to improve recovery and reduce costs.
Rats were exposed to hypoxia (3 weeks living at ½ an atmosphere). After acclimation, capillary density was measured morphometrically and was increased by 30% in the cortex. Novel implantable oxygen sensors showed that partial pressure of oxygen in the brain was increased by 40% in the normal cortex. Infarcts were induced in brain with 1 h reversible middle cerebral artery occlusions. After ischemia (48 h) behavioural scores were improved and T2 weighted MRI lesion volumes were reduced by 52% in acclimated groups. There was a reduction in inflammation indicated by reduced lymphocytes (by 27-33%), and ED1 positive cells (by 35-45%).
It is possible to stimulate a natural adaptive mechanism in the brain which will reduce damage and improve outcome for a given ischemic event. Since these adaptations occur after factors such as HIF-1α have returned to baseline, protection is likely related more to morphological changes such as angiogenesis. Such pre-conditioning, perhaps with exercise or pharmaceuticals, would not necessarily reduce the incidence of stroke, but the severity of damage could be reduced by 50%.</description><subject>Acclimation</subject><subject>Acclimatization</subject><subject>Adaptation</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Biology</subject><subject>Brain</subject><subject>Brain - blood supply</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Brain damage</subject><subject>Brain injury</subject><subject>Capillarity</subject><subject>Cerebral Infarction - pathology</subject><subject>Cerebral Infarction - physiopathology</subject><subject>Exercise</subject><subject>Hypoxia</subject><subject>Hypoxia, Brain - complications</subject><subject>Hypoxia, Brain - physiopathology</subject><subject>Ischemia</subject><subject>Lymphocyte Count</subject><subject>Lymphocytes</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Neurosciences</subject><subject>Occlusion</subject><subject>Oxygen</subject><subject>Oxygen - metabolism</subject><subject>Oxygen probes</subject><subject>Partial Pressure</subject><subject>Physical fitness</subject><subject>Physiology</subject><subject>Preconditioning</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Risk groups</subject><subject>Rodents</subject><subject>Sensors</subject><subject>Stem cells</subject><subject>Stroke</subject><subject>Stroke - etiology</subject><subject>Stroke - pathology</subject><subject>Stroke - physiopathology</subject><subject>Stroke - prevention & control</subject><subject>Studies</subject><subject>T-Lymphocytes - immunology</subject><subject>Vascular endothelial growth factor</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1rFDEUhgdRbK3-A9EBRfRi12TyOTdCKX4sFApavQ1JJpnNOjvZJplF_70Zd1p2pBeSi3w95z05J29RPIdgCRGD7zd-CL3sljvfmyUAmEDAHxSnsEbVglYAPTxanxRPYtwAQBCn9HFxUiFQccb5afH6OkjXu74t09qUatyUyZdxCHu3N2VMwf80T4tHVnbRPJvms-L7p4_XF18Wl1efVxfnlwtN6yotlLQNapSG2DBk6wbUhmJKrIUNsIpBRRoEQA2gpJrS_ALYWGYUscQqyWSFzoqXB91d56OYCowCoooSjBmpM7E6EI2XG7ELbivDb-GlE38PfGiFDMnpzggIpJE6d0ApjCEgknNIEIJEW2kZZ1nrw5RtUFvTaNOnILuZ6Pymd2vR-r1AWY8CmgXeTgLB3wwmJrF1UZuuk73xQ3434BXOHEYZffUPen91E9XKXIDrrc959SgqzklWgYzysUvLe6g8GrN1OrvBunw-C3g3C8hMMr9SK4cYxerb1_9nr37M2TdH7NrILq2j74bkfB_nID6AOvgYg7F3TYZAjGa-7YYYzSwmM-ewF8cfdBd06170B6nf7RI</recordid><startdate>20120913</startdate><enddate>20120913</enddate><creator>Dunn, Jeff F</creator><creator>Wu, Ying</creator><creator>Zhao, Zonghang</creator><creator>Srinivasan, Sathya</creator><creator>Natah, Sirajedin S</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120913</creationdate><title>Training the brain to survive stroke</title><author>Dunn, Jeff F ; Wu, Ying ; Zhao, Zonghang ; Srinivasan, Sathya ; Natah, Sirajedin S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-bafd3dbc14e73f9d09e6465ff1d0fb71b5d300901a6c660281df7eb5f5fba7a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acclimation</topic><topic>Acclimatization</topic><topic>Adaptation</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Biology</topic><topic>Brain</topic><topic>Brain - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dunn, Jeff F</au><au>Wu, Ying</au><au>Zhao, Zonghang</au><au>Srinivasan, Sathya</au><au>Natah, Sirajedin S</au><au>Baron, Jean-Claude</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Training the brain to survive stroke</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-09-13</date><risdate>2012</risdate><volume>7</volume><issue>9</issue><spage>e45108</spage><epage>e45108</epage><pages>e45108-e45108</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Presently, little can be done to repair brain tissue after stroke damage. We hypothesized that the mammalian brain has an intrinsic capacity to adapt to low oxygen which would improve outcome from a reversible hypoxic/ischemic episode. Acclimation to chronic hypoxia causes increased capillarity and tissue oxygen levels which may improve the capacity to survive ischemia. Identification of these adaptations will lead to protocols which high risk groups could use to improve recovery and reduce costs.
Rats were exposed to hypoxia (3 weeks living at ½ an atmosphere). After acclimation, capillary density was measured morphometrically and was increased by 30% in the cortex. Novel implantable oxygen sensors showed that partial pressure of oxygen in the brain was increased by 40% in the normal cortex. Infarcts were induced in brain with 1 h reversible middle cerebral artery occlusions. After ischemia (48 h) behavioural scores were improved and T2 weighted MRI lesion volumes were reduced by 52% in acclimated groups. There was a reduction in inflammation indicated by reduced lymphocytes (by 27-33%), and ED1 positive cells (by 35-45%).
It is possible to stimulate a natural adaptive mechanism in the brain which will reduce damage and improve outcome for a given ischemic event. Since these adaptations occur after factors such as HIF-1α have returned to baseline, protection is likely related more to morphological changes such as angiogenesis. Such pre-conditioning, perhaps with exercise or pharmaceuticals, would not necessarily reduce the incidence of stroke, but the severity of damage could be reduced by 50%.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23028788</pmid><doi>10.1371/journal.pone.0045108</doi><tpages>e45108</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acclimation Acclimatization Adaptation Angiogenesis Animals Biology Brain Brain - blood supply Brain - pathology Brain - physiopathology Brain damage Brain injury Capillarity Cerebral Infarction - pathology Cerebral Infarction - physiopathology Exercise Hypoxia Hypoxia, Brain - complications Hypoxia, Brain - physiopathology Ischemia Lymphocyte Count Lymphocytes Magnetic resonance imaging Male Medicine Neurosciences Occlusion Oxygen Oxygen - metabolism Oxygen probes Partial Pressure Physical fitness Physiology Preconditioning Rats Rats, Wistar Risk groups Rodents Sensors Stem cells Stroke Stroke - etiology Stroke - pathology Stroke - physiopathology Stroke - prevention & control Studies T-Lymphocytes - immunology Vascular endothelial growth factor |
title | Training the brain to survive stroke |
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