Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.

Tumor Necrosis Factor-alpha (TNF-α) is an immunomodulatory and proinflammatory cytokine implicated in neuro-inflammation and neuronal damage in response to cerebral ischemia. The present study tested the hypothesis that anti-TNF-α agents may be protective against cerebral infarction. Transient focal...

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Autores:
Rengifo Gómez, Juliana
Tipo de recurso:
Article of investigation
Fecha de publicación:
2015
Institución:
Universidad ICESI
Repositorio:
Repositorio ICESI
Idioma:
eng
OAI Identifier:
oai:repository.icesi.edu.co:10906/79906
Acceso en línea:
http://www.ncbi.nlm.nih.gov/pubmed/25350870
http://hdl.handle.net/10906/79906
https://doi.org/10.3109/00207454.2014.980906
Palabra clave:
Biología
Biology
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
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repository_id_str
spelling Rengifo Gómez, Juliana2016-08-30T22:02:02Z2016-08-30T22:02:02Z2015-01-010020-7454http://www.ncbi.nlm.nih.gov/pubmed/25350870http://hdl.handle.net/10906/79906https://doi.org/10.3109/00207454.2014.980906instname: Universidad Icesireponame: Biblioteca Digitalrepourl: https://repository.icesi.edu.co/Tumor Necrosis Factor-alpha (TNF-α) is an immunomodulatory and proinflammatory cytokine implicated in neuro-inflammation and neuronal damage in response to cerebral ischemia. The present study tested the hypothesis that anti-TNF-α agents may be protective against cerebral infarction. Transient focal ischemia was artificially induced in anesthetized adult male Wistar rats (300-350 g) by middle cerebral artery occlusion (MCAO) with an intraluminal suture. TNF-α function was interfered with either a chimeric monoclonal antibody against TNF-α (infliximab-7 mg/kg) aiming to TNF-α soluble and membrane-attached form; or a chimeric fusion protein of TNF-α receptor-2 with a fragment crystallizable (Fc) region of IgG1 (etanercept-5 mg/kg) aiming for the TNF-α soluble form. Both agents were administered intraperitoneally 0 or 6 h after inducing ischemia. Infarct volume was measured by 2,3,5-triphenyltetrazolium chloride staining. Cerebral infarct volume was significantly reduced in either etanercept or infliximab-treated group compared with non-treated MCAO rats 24 h after reperfusion. These results suggest that anti-TNF-α agents may reduce focal ischemic injury in rats.engTaylor & FrancisInternational Journal of Neuroscience, Vol. 125, No.12 - 2015EL AUTOR, expresa que la obra objeto de la presente autorización es original y la elaboró sin quebrantar ni suplantar los derechos de autor de terceros, y de tal forma, la obra es de su exclusiva autoría y tiene la titularidad sobre éste. PARÁGRAFO: en caso de queja o acción por parte de un tercero referente a los derechos de autor sobre el artículo, folleto o libro en cuestión, EL AUTOR, asumirá la responsabilidad total, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos, la Universidad Icesi actúa como un tercero de buena fe. Esta autorización, permite a la Universidad Icesi, de forma indefinida, para que en los términos establecidos en la Ley 23 de 1982, la Ley 44 de 1993, leyes y jurisprudencia vigente al respecto, haga publicación de este con fines educativos. Toda persona que consulte ya sea la biblioteca o en medio electrónico podrá copiar apartes del texto citando siempre la fuentes, es decir el título del trabajo y el autor.https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessAtribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)http://purl.org/coar/access_right/c_abf2BiologíaBiologySoluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1Artículoinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85125ORIGINALdocumento.htmldocumento.htmltext/html298http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/79906/1/documento.html9c765e21295c94ce24f86afb35619d44MD5110906/79906oai:repository.icesi.edu.co:10906/799062018-10-22 14:57:28.924Biblioteca Digital - Universidad icesicdcriollo@icesi.edu.co
dc.title.spa.fl_str_mv Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
title Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
spellingShingle Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
Biología
Biology
title_short Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
title_full Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
title_fullStr Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
title_full_unstemmed Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
title_sort Soluble or soluble/membrane TNF-α inhibitors protect the brain from focal ischemic injury in rats.
dc.creator.fl_str_mv Rengifo Gómez, Juliana
dc.contributor.author.spa.fl_str_mv Rengifo Gómez, Juliana
dc.subject.none.fl_str_mv Biología
Biology
topic Biología
Biology
description Tumor Necrosis Factor-alpha (TNF-α) is an immunomodulatory and proinflammatory cytokine implicated in neuro-inflammation and neuronal damage in response to cerebral ischemia. The present study tested the hypothesis that anti-TNF-α agents may be protective against cerebral infarction. Transient focal ischemia was artificially induced in anesthetized adult male Wistar rats (300-350 g) by middle cerebral artery occlusion (MCAO) with an intraluminal suture. TNF-α function was interfered with either a chimeric monoclonal antibody against TNF-α (infliximab-7 mg/kg) aiming to TNF-α soluble and membrane-attached form; or a chimeric fusion protein of TNF-α receptor-2 with a fragment crystallizable (Fc) region of IgG1 (etanercept-5 mg/kg) aiming for the TNF-α soluble form. Both agents were administered intraperitoneally 0 or 6 h after inducing ischemia. Infarct volume was measured by 2,3,5-triphenyltetrazolium chloride staining. Cerebral infarct volume was significantly reduced in either etanercept or infliximab-treated group compared with non-treated MCAO rats 24 h after reperfusion. These results suggest that anti-TNF-α agents may reduce focal ischemic injury in rats.
publishDate 2015
dc.date.issued.none.fl_str_mv 2015-01-01
dc.date.accessioned.none.fl_str_mv 2016-08-30T22:02:02Z
dc.date.available.none.fl_str_mv 2016-08-30T22:02:02Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.coar.none.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.local.none.fl_str_mv Artículo
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dc.identifier.other.spa.fl_str_mv http://www.ncbi.nlm.nih.gov/pubmed/25350870
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10906/79906
dc.identifier.doi.none.fl_str_mv https://doi.org/10.3109/00207454.2014.980906
dc.identifier.instname.none.fl_str_mv instname: Universidad Icesi
dc.identifier.reponame.none.fl_str_mv reponame: Biblioteca Digital
dc.identifier.repourl.none.fl_str_mv repourl: https://repository.icesi.edu.co/
identifier_str_mv 0020-7454
instname: Universidad Icesi
reponame: Biblioteca Digital
repourl: https://repository.icesi.edu.co/
url http://www.ncbi.nlm.nih.gov/pubmed/25350870
http://hdl.handle.net/10906/79906
https://doi.org/10.3109/00207454.2014.980906
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv International Journal of Neuroscience, Vol. 125, No.12 - 2015
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.accessrights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.license.none.fl_str_mv Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
dc.rights.coar.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.publisher.spa.fl_str_mv Taylor & Francis
institution Universidad ICESI
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