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Extravasation of Microspheres in a Rat Model of Silent Brain Infarcts
BACKGROUND AND PURPOSE—We developed a rat model of silent brain infarcts based on microsphere infusion and investigated their impact on perfusion and tissue damage. Second, we studied the extent and mechanisms of perfusion recovery. METHODS—At day 0, 15 µm fluorescent microspheres were injected into...
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Published in: | Stroke (1970) 2019-06, Vol.50 (6), p.1590-1594 |
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container_title | Stroke (1970) |
container_volume | 50 |
creator | van der Wijk, Anne-Eva Lachkar, Nadia de Vos, Judith Grootemaat, Anita E van der Wel, Nicole N Hordijk, Peter L Bakker, Erik N.T.P vanBavel, Ed |
description | BACKGROUND AND PURPOSE—We developed a rat model of silent brain infarcts based on microsphere infusion and investigated their impact on perfusion and tissue damage. Second, we studied the extent and mechanisms of perfusion recovery.
METHODS—At day 0, 15 µm fluorescent microspheres were injected into the right common carotid artery of F344 rats. At days 1, 7, or 28, the brain was removed, cut in 100-µm cryosections, and processed for immunofluorescent staining and analysis.
RESULTS—Injection of microspheres caused mild and transient damage to the treated hemisphere, with a decrease in perfused capillary volume at day 1, as compared with the untreated hemisphere. At day 1 but not at days 7 and 28, we observed IgG staining outside of the vessels, indicating vessel leakage. All microspheres were located inside the lumen of the vessels at day 1, whereas the vast majority (≈80%) of the microspheres were extravascular at day 7, and 100% at day 28. This was accompanied by restoration of perfused capillary volume.
CONCLUSIONS—Microspheres cause mild and transient damage, and effective extravasation mechanisms exist in the brain to clear microsized emboli from the vessels. |
doi_str_mv | 10.1161/STROKEAHA.119.024975 |
format | article |
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METHODS—At day 0, 15 µm fluorescent microspheres were injected into the right common carotid artery of F344 rats. At days 1, 7, or 28, the brain was removed, cut in 100-µm cryosections, and processed for immunofluorescent staining and analysis.
RESULTS—Injection of microspheres caused mild and transient damage to the treated hemisphere, with a decrease in perfused capillary volume at day 1, as compared with the untreated hemisphere. At day 1 but not at days 7 and 28, we observed IgG staining outside of the vessels, indicating vessel leakage. All microspheres were located inside the lumen of the vessels at day 1, whereas the vast majority (≈80%) of the microspheres were extravascular at day 7, and 100% at day 28. This was accompanied by restoration of perfused capillary volume.
CONCLUSIONS—Microspheres cause mild and transient damage, and effective extravasation mechanisms exist in the brain to clear microsized emboli from the vessels.</description><identifier>ISSN: 0039-2499</identifier><identifier>EISSN: 1524-4628</identifier><identifier>DOI: 10.1161/STROKEAHA.119.024975</identifier><identifier>PMID: 31136287</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Animals ; Brain Infarction - chemically induced ; Brain Infarction - metabolism ; Brain Infarction - pathology ; Disease Models, Animal ; Male ; Microspheres ; Rats ; Rats, Inbred F344</subject><ispartof>Stroke (1970), 2019-06, Vol.50 (6), p.1590-1594</ispartof><rights>2019 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4025-865d130e75b819052152e8fb4a1842953b3bbd3d8c4ea6c837e674321ec9842e3</citedby><cites>FETCH-LOGICAL-c4025-865d130e75b819052152e8fb4a1842953b3bbd3d8c4ea6c837e674321ec9842e3</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/31136287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Wijk, Anne-Eva</creatorcontrib><creatorcontrib>Lachkar, Nadia</creatorcontrib><creatorcontrib>de Vos, Judith</creatorcontrib><creatorcontrib>Grootemaat, Anita E</creatorcontrib><creatorcontrib>van der Wel, Nicole N</creatorcontrib><creatorcontrib>Hordijk, Peter L</creatorcontrib><creatorcontrib>Bakker, Erik N.T.P</creatorcontrib><creatorcontrib>vanBavel, Ed</creatorcontrib><title>Extravasation of Microspheres in a Rat Model of Silent Brain Infarcts</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>BACKGROUND AND PURPOSE—We developed a rat model of silent brain infarcts based on microsphere infusion and investigated their impact on perfusion and tissue damage. Second, we studied the extent and mechanisms of perfusion recovery.
METHODS—At day 0, 15 µm fluorescent microspheres were injected into the right common carotid artery of F344 rats. At days 1, 7, or 28, the brain was removed, cut in 100-µm cryosections, and processed for immunofluorescent staining and analysis.
RESULTS—Injection of microspheres caused mild and transient damage to the treated hemisphere, with a decrease in perfused capillary volume at day 1, as compared with the untreated hemisphere. At day 1 but not at days 7 and 28, we observed IgG staining outside of the vessels, indicating vessel leakage. All microspheres were located inside the lumen of the vessels at day 1, whereas the vast majority (≈80%) of the microspheres were extravascular at day 7, and 100% at day 28. This was accompanied by restoration of perfused capillary volume.
CONCLUSIONS—Microspheres cause mild and transient damage, and effective extravasation mechanisms exist in the brain to clear microsized emboli from the vessels.</description><subject>Animals</subject><subject>Brain Infarction - chemically induced</subject><subject>Brain Infarction - metabolism</subject><subject>Brain Infarction - pathology</subject><subject>Disease Models, Animal</subject><subject>Male</subject><subject>Microspheres</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><issn>0039-2499</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE9PwkAQxTdGI4h-A2N69FLcf213j2iqECEkgOfNtp2G6tLibhH99i4pcvQ0mbzfvJl5CN0SPCQkJg_L1WL-mo7GI9_KIaZcJtEZ6pOI8pDHVJyjPsZMhl6QPXTl3DvGmDIRXaIeI4R5JOmjNP1urf7STrdVUwdNGcyq3DZuuwYLLqjqQAcL3QazpgBzkJeVgboNHq322qQutc1bd40uSm0c3BzrAL09p6uncTidv0yeRtMw55hGoYijgjAMSZQJInFE_bEgyoxrIjiVEctYlhWsEDkHHeeCJRAnnFECufQAsAG673y3tvncgWvVpnI5GKNraHZOUcq8U0K81QDxDj184yyUamurjbY_imB1CFCdAvStVF2AfuzuuGGXbaA4Df0l5gHRAfvGtGDdh9ntwao1aNOu__f-BTLJfLM</recordid><startdate>201906</startdate><enddate>201906</enddate><creator>van der Wijk, Anne-Eva</creator><creator>Lachkar, Nadia</creator><creator>de Vos, Judith</creator><creator>Grootemaat, Anita E</creator><creator>van der Wel, Nicole N</creator><creator>Hordijk, Peter L</creator><creator>Bakker, Erik N.T.P</creator><creator>vanBavel, Ed</creator><general>American Heart Association, Inc</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>7X8</scope></search><sort><creationdate>201906</creationdate><title>Extravasation of Microspheres in a Rat Model of Silent Brain Infarcts</title><author>van der Wijk, Anne-Eva ; Lachkar, Nadia ; de Vos, Judith ; Grootemaat, Anita E ; van der Wel, Nicole N ; Hordijk, Peter L ; Bakker, Erik N.T.P ; vanBavel, Ed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4025-865d130e75b819052152e8fb4a1842953b3bbd3d8c4ea6c837e674321ec9842e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Brain Infarction - chemically induced</topic><topic>Brain Infarction - metabolism</topic><topic>Brain Infarction - pathology</topic><topic>Disease Models, Animal</topic><topic>Male</topic><topic>Microspheres</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Wijk, Anne-Eva</creatorcontrib><creatorcontrib>Lachkar, Nadia</creatorcontrib><creatorcontrib>de Vos, Judith</creatorcontrib><creatorcontrib>Grootemaat, Anita E</creatorcontrib><creatorcontrib>van der Wel, Nicole N</creatorcontrib><creatorcontrib>Hordijk, Peter L</creatorcontrib><creatorcontrib>Bakker, Erik N.T.P</creatorcontrib><creatorcontrib>vanBavel, Ed</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Wijk, Anne-Eva</au><au>Lachkar, Nadia</au><au>de Vos, Judith</au><au>Grootemaat, Anita E</au><au>van der Wel, Nicole N</au><au>Hordijk, Peter L</au><au>Bakker, Erik N.T.P</au><au>vanBavel, Ed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extravasation of Microspheres in a Rat Model of Silent Brain Infarcts</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2019-06</date><risdate>2019</risdate><volume>50</volume><issue>6</issue><spage>1590</spage><epage>1594</epage><pages>1590-1594</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><abstract>BACKGROUND AND PURPOSE—We developed a rat model of silent brain infarcts based on microsphere infusion and investigated their impact on perfusion and tissue damage. Second, we studied the extent and mechanisms of perfusion recovery.
METHODS—At day 0, 15 µm fluorescent microspheres were injected into the right common carotid artery of F344 rats. At days 1, 7, or 28, the brain was removed, cut in 100-µm cryosections, and processed for immunofluorescent staining and analysis.
RESULTS—Injection of microspheres caused mild and transient damage to the treated hemisphere, with a decrease in perfused capillary volume at day 1, as compared with the untreated hemisphere. At day 1 but not at days 7 and 28, we observed IgG staining outside of the vessels, indicating vessel leakage. All microspheres were located inside the lumen of the vessels at day 1, whereas the vast majority (≈80%) of the microspheres were extravascular at day 7, and 100% at day 28. This was accompanied by restoration of perfused capillary volume.
CONCLUSIONS—Microspheres cause mild and transient damage, and effective extravasation mechanisms exist in the brain to clear microsized emboli from the vessels.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>31136287</pmid><doi>10.1161/STROKEAHA.119.024975</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Alma/SFX Local Collection |
subjects | Animals Brain Infarction - chemically induced Brain Infarction - metabolism Brain Infarction - pathology Disease Models, Animal Male Microspheres Rats Rats, Inbred F344 |
title | Extravasation of Microspheres in a Rat Model of Silent Brain Infarcts |
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