Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury

Apoptosis is one of the most destructive mechanisms that develop after spinal cord (SC) injury. Immunization with neural-derived peptides (INDPs) such as A91 has shown to reduce the deleterious proinflammatory response and the amount of harmful compounds produced after SC injury. With the notion tha...

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Main Authors: Roxana Rodríguez-Barrera, Ana M. Fernández-Presas, Elisa García, Adrian Flores-Romero, Susana Martiñón, Viridiana Yazmín González-Puertos, Humberto Mestre, Carmina Flores-Dominguez, Verónica Rodriguez-Mata, Mina Königsberg, Sandra Solano, Antonio Ibarra
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2013/827517
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spelling doaj-1052a7323b29465ebba43fc492b40e1f2020-11-24T23:28:47ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/827517827517Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic InjuryRoxana Rodríguez-Barrera0Ana M. Fernández-Presas1Elisa García2Adrian Flores-Romero3Susana Martiñón4Viridiana Yazmín González-Puertos5Humberto Mestre6Carmina Flores-Dominguez7Verónica Rodriguez-Mata8Mina Königsberg9Sandra Solano10Antonio Ibarra11Facultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoDepartamento de Microbiología y Parasitología, Facultad de Medicina, UNAM, DF, CP 04510, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoDepartamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana Iztapalapa, DF, CP 09340, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoDepartamento de Microbiología y Parasitología, Facultad de Medicina, UNAM, DF, CP 04510, MexicoDepartamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana Iztapalapa, DF, CP 09340, MexicoDepartamento de Microbiología y Parasitología, Facultad de Medicina, UNAM, DF, CP 04510, MexicoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Edo. de México, CP 52786, MexicoApoptosis is one of the most destructive mechanisms that develop after spinal cord (SC) injury. Immunization with neural-derived peptides (INDPs) such as A91 has shown to reduce the deleterious proinflammatory response and the amount of harmful compounds produced after SC injury. With the notion that the aforementioned elements are apoptotic inducers, we hypothesized that INDPs would reduce apoptosis after SC injury. In order to test this assumption, adult rats were subjected to SC contusion and immunized either with A91 or phosphate buffered saline (PBS; control group). Seven days after injury, animals were euthanized to evaluate the number of apoptotic cells at the injury site. Apoptosis was evaluated using DAPI and TUNEL techniques; caspase-3 activity was also evaluated. To further elucidate the mechanisms through which A91 exerts this antiapoptotic effects we quantified tumor necrosis factor-alpha (TNF-α). To also demonstrate that the decrease in apoptotic cells correlated with a functional improvement, locomotor recovery was evaluated. Immunization with A91 significantly reduced the number of apoptotic cells and decreased caspase-3 activity and TNF-α concentration. Immunization with A91 also improved the functional recovery of injured rats. The present study shows the beneficial effect of INDPs on preventing apoptosis and provides more evidence on the neuroprotective mechanisms exerted by this strategy.http://dx.doi.org/10.1155/2013/827517
collection DOAJ
language English
format Article
sources DOAJ
author Roxana Rodríguez-Barrera
Ana M. Fernández-Presas
Elisa García
Adrian Flores-Romero
Susana Martiñón
Viridiana Yazmín González-Puertos
Humberto Mestre
Carmina Flores-Dominguez
Verónica Rodriguez-Mata
Mina Königsberg
Sandra Solano
Antonio Ibarra
spellingShingle Roxana Rodríguez-Barrera
Ana M. Fernández-Presas
Elisa García
Adrian Flores-Romero
Susana Martiñón
Viridiana Yazmín González-Puertos
Humberto Mestre
Carmina Flores-Dominguez
Verónica Rodriguez-Mata
Mina Königsberg
Sandra Solano
Antonio Ibarra
Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
BioMed Research International
author_facet Roxana Rodríguez-Barrera
Ana M. Fernández-Presas
Elisa García
Adrian Flores-Romero
Susana Martiñón
Viridiana Yazmín González-Puertos
Humberto Mestre
Carmina Flores-Dominguez
Verónica Rodriguez-Mata
Mina Königsberg
Sandra Solano
Antonio Ibarra
author_sort Roxana Rodríguez-Barrera
title Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
title_short Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
title_full Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
title_fullStr Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
title_full_unstemmed Immunization with a Neural-Derived Peptide Protects the Spinal Cord from Apoptosis after Traumatic Injury
title_sort immunization with a neural-derived peptide protects the spinal cord from apoptosis after traumatic injury
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2013-01-01
description Apoptosis is one of the most destructive mechanisms that develop after spinal cord (SC) injury. Immunization with neural-derived peptides (INDPs) such as A91 has shown to reduce the deleterious proinflammatory response and the amount of harmful compounds produced after SC injury. With the notion that the aforementioned elements are apoptotic inducers, we hypothesized that INDPs would reduce apoptosis after SC injury. In order to test this assumption, adult rats were subjected to SC contusion and immunized either with A91 or phosphate buffered saline (PBS; control group). Seven days after injury, animals were euthanized to evaluate the number of apoptotic cells at the injury site. Apoptosis was evaluated using DAPI and TUNEL techniques; caspase-3 activity was also evaluated. To further elucidate the mechanisms through which A91 exerts this antiapoptotic effects we quantified tumor necrosis factor-alpha (TNF-α). To also demonstrate that the decrease in apoptotic cells correlated with a functional improvement, locomotor recovery was evaluated. Immunization with A91 significantly reduced the number of apoptotic cells and decreased caspase-3 activity and TNF-α concentration. Immunization with A91 also improved the functional recovery of injured rats. The present study shows the beneficial effect of INDPs on preventing apoptosis and provides more evidence on the neuroprotective mechanisms exerted by this strategy.
url http://dx.doi.org/10.1155/2013/827517
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