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Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation

Acute ischemia-reperfusion injury (IRI) of the extremities leads to local and systemic inflammatory changes which can hinder limb function and can be life threatening. This study examined whether the administration of the T-cell sequestration agent, FTY720, following hind limb tourniquet-induced ske...

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Autores principales: Foster, Anthony D., Vicente, Diego, Sexton, Jonathan J., Johnston, Luke, Clark, Nick, Leonhardt, Crystal, Elster, Eric A., Davis, Thomas A., Bradley, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749296/
https://www.ncbi.nlm.nih.gov/pubmed/29410598
http://dx.doi.org/10.1155/2017/4594035
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author Foster, Anthony D.
Vicente, Diego
Sexton, Jonathan J.
Johnston, Luke
Clark, Nick
Leonhardt, Crystal
Elster, Eric A.
Davis, Thomas A.
Bradley, Matthew J.
author_facet Foster, Anthony D.
Vicente, Diego
Sexton, Jonathan J.
Johnston, Luke
Clark, Nick
Leonhardt, Crystal
Elster, Eric A.
Davis, Thomas A.
Bradley, Matthew J.
author_sort Foster, Anthony D.
collection PubMed
description Acute ischemia-reperfusion injury (IRI) of the extremities leads to local and systemic inflammatory changes which can hinder limb function and can be life threatening. This study examined whether the administration of the T-cell sequestration agent, FTY720, following hind limb tourniquet-induced skeletal muscle IRI in a rat model would attenuate systemic inflammation and multiple end organ injury. Sprague-Dawley rats were subjected to 1 hr of ischemia via application of a rubber band tourniquet. Animals were randomized to receive an intravenous bolus of either vehicle control or FTY720 15 min after band placement. Rats (n = 10/time point) were euthanized at 6, 24, and 72 hr post-IRI. Peripheral blood as well as lung, liver, kidney, and ischemic muscle tissue was analyzed and compared between groups. FTY720 treatment markedly decreased the number of peripheral blood T cells (p < 0.05) resulting in a decreased systemic inflammatory response and lower serum creatinine levels and had a modest but significant effect in decreasing the transcription of injury-associated target genes in multiple end organs. These findings suggest that early intervention with FTY720 may benefit the treatment of IRI of the limb. Further preclinical studies are necessary to characterize the short-term and long-term beneficial effects of FTY720 following tourniquet-induced IRI.
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spelling pubmed-57492962018-02-06 Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation Foster, Anthony D. Vicente, Diego Sexton, Jonathan J. Johnston, Luke Clark, Nick Leonhardt, Crystal Elster, Eric A. Davis, Thomas A. Bradley, Matthew J. Mediators Inflamm Research Article Acute ischemia-reperfusion injury (IRI) of the extremities leads to local and systemic inflammatory changes which can hinder limb function and can be life threatening. This study examined whether the administration of the T-cell sequestration agent, FTY720, following hind limb tourniquet-induced skeletal muscle IRI in a rat model would attenuate systemic inflammation and multiple end organ injury. Sprague-Dawley rats were subjected to 1 hr of ischemia via application of a rubber band tourniquet. Animals were randomized to receive an intravenous bolus of either vehicle control or FTY720 15 min after band placement. Rats (n = 10/time point) were euthanized at 6, 24, and 72 hr post-IRI. Peripheral blood as well as lung, liver, kidney, and ischemic muscle tissue was analyzed and compared between groups. FTY720 treatment markedly decreased the number of peripheral blood T cells (p < 0.05) resulting in a decreased systemic inflammatory response and lower serum creatinine levels and had a modest but significant effect in decreasing the transcription of injury-associated target genes in multiple end organs. These findings suggest that early intervention with FTY720 may benefit the treatment of IRI of the limb. Further preclinical studies are necessary to characterize the short-term and long-term beneficial effects of FTY720 following tourniquet-induced IRI. Hindawi 2017 2017-12-19 /pmc/articles/PMC5749296/ /pubmed/29410598 http://dx.doi.org/10.1155/2017/4594035 Text en Copyright © 2017 Anthony D. Foster et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Foster, Anthony D.
Vicente, Diego
Sexton, Jonathan J.
Johnston, Luke
Clark, Nick
Leonhardt, Crystal
Elster, Eric A.
Davis, Thomas A.
Bradley, Matthew J.
Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title_full Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title_fullStr Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title_full_unstemmed Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title_short Administration of FTY720 during Tourniquet-Induced Limb Ischemia Reperfusion Injury Attenuates Systemic Inflammation
title_sort administration of fty720 during tourniquet-induced limb ischemia reperfusion injury attenuates systemic inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749296/
https://www.ncbi.nlm.nih.gov/pubmed/29410598
http://dx.doi.org/10.1155/2017/4594035
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