What is the restorative effect of VEGF inhibitor bevacuzimab against subarachnoid hemorrhage in an experimental model
This study investigated the effect of vascular endothelial growth factor (VEGF) inhibitor bevacuzimab (BVZ) on the rabbit basilar artery using an experimental subarachnoid hemorrhage (SAH) model. Eighteen adult male New-Zealand white rabbits were randomly divided into three groups: a control group (...
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Veröffentlicht in: | TURKISH JOURNAL OF MEDICAL SCIENCES 2021-01, Vol.51 (5), p.2698-2704 |
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creator | Demİrcİ, Adnan YalÇin GÜvenÇ, Yahya Özeren, Ersİn Akyol, Çetİn Bayram, Pinar Bİllur, Denİz Aydin, Sevİm SeÇkİn, Hakan YİĞİtkanli, Kazim |
description | This study investigated the effect of vascular endothelial growth factor (VEGF) inhibitor bevacuzimab (BVZ) on the rabbit basilar artery using an experimental subarachnoid hemorrhage (SAH) model.
Eighteen adult male New-Zealand white rabbits were randomly divided into three groups: a control group (n=6), SAH group (n=6), and SAH+BVZ group (n=6). Experimental SAH was created by injecting autologous arterial blood into the cisterna magna. In the treatment group, the subjects were administered a daily dose of 10 mg/kg, intravenous BVZ 2 days after the SAH. Basilar artery diameters were measured with magnetic resonance angiography (MRA) 72 hours after the SAH in all groups. After 72 hours the animals? whole brains, including the upper cervical region, were obtained from all the animals after perfusion and fixation of the animal. The wall thickness, luminal area, and the apoptosis at the basilar arteries were evaluated in all groups.
BVZ significantly prevented SAH induced vasospasm confirmed in-vivo with MRA imaging with additional suppression of apoptosis on basilar artery wall.
VEGF inhibition with BVZ has shown to have a vasospasm and apoptosis attenuating effect on basilar artery in a SAH model. |
doi_str_mv | 10.3906/sag-2001-230 |
format | Article |
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Eighteen adult male New-Zealand white rabbits were randomly divided into three groups: a control group (n=6), SAH group (n=6), and SAH+BVZ group (n=6). Experimental SAH was created by injecting autologous arterial blood into the cisterna magna. In the treatment group, the subjects were administered a daily dose of 10 mg/kg, intravenous BVZ 2 days after the SAH. Basilar artery diameters were measured with magnetic resonance angiography (MRA) 72 hours after the SAH in all groups. After 72 hours the animals? whole brains, including the upper cervical region, were obtained from all the animals after perfusion and fixation of the animal. The wall thickness, luminal area, and the apoptosis at the basilar arteries were evaluated in all groups.
BVZ significantly prevented SAH induced vasospasm confirmed in-vivo with MRA imaging with additional suppression of apoptosis on basilar artery wall.
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Eighteen adult male New-Zealand white rabbits were randomly divided into three groups: a control group (n=6), SAH group (n=6), and SAH+BVZ group (n=6). Experimental SAH was created by injecting autologous arterial blood into the cisterna magna. In the treatment group, the subjects were administered a daily dose of 10 mg/kg, intravenous BVZ 2 days after the SAH. Basilar artery diameters were measured with magnetic resonance angiography (MRA) 72 hours after the SAH in all groups. After 72 hours the animals? whole brains, including the upper cervical region, were obtained from all the animals after perfusion and fixation of the animal. The wall thickness, luminal area, and the apoptosis at the basilar arteries were evaluated in all groups.
BVZ significantly prevented SAH induced vasospasm confirmed in-vivo with MRA imaging with additional suppression of apoptosis on basilar artery wall.
VEGF inhibition with BVZ has shown to have a vasospasm and apoptosis attenuating effect on basilar artery in a SAH model.</description><issn>1303-6165</issn><issn>1303-6165</issn><fulltext>false</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpNkE1LAzEQhoMoWqo3z5If4Gqy2U03RyltFQpe_Dguk82kG-juliRb1F9vSlU8zcA8M8z7EHLN2Z1QTN4H2GQ5YzzLBTshEy6YyCSX5em__pxcCCFKyfJiQsb3FiJ1gcYWqccQBw_R7ZGitdhEOlj6tlgtqetbp12aUo17aMYv14GmsAHXh0jDqMFD0_aDM7TFbvC-hQ2mLQo9xY8detdhH2FLu8Hg9pKcWdgGvPqpU_K6XLzMH7P18-pp_rDOmrySMSu5bnKp8rxK2SojCqW0AGMKrRRXTKsClSlRIyosLDNalTPFwaqq0rOZlWxKbo93Gz-E4NHWu_QI-M-as_ogrE7C6oOwOglL-M0R3426Q_MH_-pi3_ayagw</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Demİrcİ, Adnan YalÇin</creator><creator>GÜvenÇ, Yahya</creator><creator>Özeren, Ersİn</creator><creator>Akyol, Çetİn</creator><creator>Bayram, Pinar</creator><creator>Bİllur, Denİz</creator><creator>Aydin, Sevİm</creator><creator>SeÇkİn, Hakan</creator><creator>YİĞİtkanli, Kazim</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-4813-0854</orcidid><orcidid>https://orcid.org/0000-0001-9924-7051</orcidid><orcidid>https://orcid.org/0000-0002-7759-7568</orcidid><orcidid>https://orcid.org/0000-0001-9861-274X</orcidid><orcidid>https://orcid.org/0000-0003-1738-5923</orcidid><orcidid>https://orcid.org/0000-0003-0628-0173</orcidid><orcidid>https://orcid.org/0000-0002-5791-0094</orcidid><orcidid>https://orcid.org/0000-0001-8541-8251</orcidid><orcidid>https://orcid.org/0000-0001-6413-7362</orcidid></search><sort><creationdate>20210101</creationdate><title>What is the restorative effect of VEGF inhibitor bevacuzimab against subarachnoid hemorrhage in an experimental model</title><author>Demİrcİ, Adnan YalÇin ; GÜvenÇ, Yahya ; Özeren, Ersİn ; Akyol, Çetİn ; Bayram, Pinar ; Bİllur, Denİz ; Aydin, Sevİm ; SeÇkİn, Hakan ; YİĞİtkanli, Kazim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-51bc2692289068d3499b3add4b99190b94e9d5ebee9e4f0db95791af988b77f60</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><creatorcontrib>Demİrcİ, Adnan YalÇin</creatorcontrib><creatorcontrib>GÜvenÇ, Yahya</creatorcontrib><creatorcontrib>Özeren, Ersİn</creatorcontrib><creatorcontrib>Akyol, Çetİn</creatorcontrib><creatorcontrib>Bayram, Pinar</creatorcontrib><creatorcontrib>Bİllur, Denİz</creatorcontrib><creatorcontrib>Aydin, Sevİm</creatorcontrib><creatorcontrib>SeÇkİn, Hakan</creatorcontrib><creatorcontrib>YİĞİtkanli, Kazim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>TURKISH JOURNAL OF MEDICAL SCIENCES</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>no_fulltext</fulltext></delivery><addata><au>Demİrcİ, Adnan YalÇin</au><au>GÜvenÇ, Yahya</au><au>Özeren, Ersİn</au><au>Akyol, Çetİn</au><au>Bayram, Pinar</au><au>Bİllur, Denİz</au><au>Aydin, Sevİm</au><au>SeÇkİn, Hakan</au><au>YİĞİtkanli, Kazim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>What is the restorative effect of VEGF inhibitor bevacuzimab against subarachnoid hemorrhage in an experimental model</atitle><jtitle>TURKISH JOURNAL OF MEDICAL SCIENCES</jtitle><addtitle>Turk J Med Sci</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>51</volume><issue>5</issue><spage>2698</spage><epage>2704</epage><pages>2698-2704</pages><issn>1303-6165</issn><eissn>1303-6165</eissn><abstract>This study investigated the effect of vascular endothelial growth factor (VEGF) inhibitor bevacuzimab (BVZ) on the rabbit basilar artery using an experimental subarachnoid hemorrhage (SAH) model.
Eighteen adult male New-Zealand white rabbits were randomly divided into three groups: a control group (n=6), SAH group (n=6), and SAH+BVZ group (n=6). Experimental SAH was created by injecting autologous arterial blood into the cisterna magna. In the treatment group, the subjects were administered a daily dose of 10 mg/kg, intravenous BVZ 2 days after the SAH. Basilar artery diameters were measured with magnetic resonance angiography (MRA) 72 hours after the SAH in all groups. After 72 hours the animals? whole brains, including the upper cervical region, were obtained from all the animals after perfusion and fixation of the animal. The wall thickness, luminal area, and the apoptosis at the basilar arteries were evaluated in all groups.
BVZ significantly prevented SAH induced vasospasm confirmed in-vivo with MRA imaging with additional suppression of apoptosis on basilar artery wall.
VEGF inhibition with BVZ has shown to have a vasospasm and apoptosis attenuating effect on basilar artery in a SAH model.</abstract><cop>Turkey</cop><pmid>33356024</pmid><doi>10.3906/sag-2001-230</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4813-0854</orcidid><orcidid>https://orcid.org/0000-0001-9924-7051</orcidid><orcidid>https://orcid.org/0000-0002-7759-7568</orcidid><orcidid>https://orcid.org/0000-0001-9861-274X</orcidid><orcidid>https://orcid.org/0000-0003-1738-5923</orcidid><orcidid>https://orcid.org/0000-0003-0628-0173</orcidid><orcidid>https://orcid.org/0000-0002-5791-0094</orcidid><orcidid>https://orcid.org/0000-0001-8541-8251</orcidid><orcidid>https://orcid.org/0000-0001-6413-7362</orcidid><oa>free_for_read</oa></addata></record> |
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title | What is the restorative effect of VEGF inhibitor bevacuzimab against subarachnoid hemorrhage in an experimental model |
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