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Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection
BACKGROUND: Iron oxide nanoparticles (IONPs) can attenuate oxidative stress in a neutral pH environment in vitro. In combination with an external electromagnetic field, they can also facilitate axon regeneration. The present study demonstrates the in vivo potential of IONPs to recover functional def...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693820/ https://www.ncbi.nlm.nih.gov/pubmed/23818782 http://dx.doi.org/10.2147/IJN.S44238 |
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author | Pal, Ajay Singh, Anand Nag, Tapas C Chattopadhyay, Parthaprasad Mathur, Rashmi Jain, Suman |
author_facet | Pal, Ajay Singh, Anand Nag, Tapas C Chattopadhyay, Parthaprasad Mathur, Rashmi Jain, Suman |
author_sort | Pal, Ajay |
collection | PubMed |
description | BACKGROUND: Iron oxide nanoparticles (IONPs) can attenuate oxidative stress in a neutral pH environment in vitro. In combination with an external electromagnetic field, they can also facilitate axon regeneration. The present study demonstrates the in vivo potential of IONPs to recover functional deficits in rats with complete spinal cord injury. METHODS: The spinal cord was completely transected at the T11 vertebra in male albino Wistar rats. Iron oxide nanoparticle solution (25 μg/mL) embedded in 3% agarose gel was implanted at the site of transection, which was subsequently exposed to an electromagnetic field (50 Hz, 17.96 μT for two hours daily for five weeks). RESULTS: Locomotor and sensorimotor assessment as well as histological analysis demonstrated significant functional recovery and a reduction in lesion volume in rats with IONP implantation and exposure to an electromagnetic field. No collagenous scar was observed and IONPs were localized intracellularly in the immediate vicinity of the lesion. Further, in vitro experiments to explore the cytotoxic effects of IONPs showed no effect on cell survival. However, a significant decrease in H(2)O(2)-mediated oxidative stress was evident in the medium containing IONPs, indicating their free radical scavenging properties. CONCLUSION: These novel findings indicate a therapeutic role for IONPs in spinal cord injury and other neurodegenerative disorders mediated by reactive oxygen species. |
format | Online Article Text |
id | pubmed-3693820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36938202013-07-01 Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection Pal, Ajay Singh, Anand Nag, Tapas C Chattopadhyay, Parthaprasad Mathur, Rashmi Jain, Suman Int J Nanomedicine Original Research BACKGROUND: Iron oxide nanoparticles (IONPs) can attenuate oxidative stress in a neutral pH environment in vitro. In combination with an external electromagnetic field, they can also facilitate axon regeneration. The present study demonstrates the in vivo potential of IONPs to recover functional deficits in rats with complete spinal cord injury. METHODS: The spinal cord was completely transected at the T11 vertebra in male albino Wistar rats. Iron oxide nanoparticle solution (25 μg/mL) embedded in 3% agarose gel was implanted at the site of transection, which was subsequently exposed to an electromagnetic field (50 Hz, 17.96 μT for two hours daily for five weeks). RESULTS: Locomotor and sensorimotor assessment as well as histological analysis demonstrated significant functional recovery and a reduction in lesion volume in rats with IONP implantation and exposure to an electromagnetic field. No collagenous scar was observed and IONPs were localized intracellularly in the immediate vicinity of the lesion. Further, in vitro experiments to explore the cytotoxic effects of IONPs showed no effect on cell survival. However, a significant decrease in H(2)O(2)-mediated oxidative stress was evident in the medium containing IONPs, indicating their free radical scavenging properties. CONCLUSION: These novel findings indicate a therapeutic role for IONPs in spinal cord injury and other neurodegenerative disorders mediated by reactive oxygen species. Dove Medical Press 2013 2013-06-21 /pmc/articles/PMC3693820/ /pubmed/23818782 http://dx.doi.org/10.2147/IJN.S44238 Text en © 2013 Pal et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Pal, Ajay Singh, Anand Nag, Tapas C Chattopadhyay, Parthaprasad Mathur, Rashmi Jain, Suman Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title | Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title_full | Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title_fullStr | Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title_full_unstemmed | Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title_short | Iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
title_sort | iron oxide nanoparticles and magnetic field exposure promote functional recovery by attenuating free radical-induced damage in rats with spinal cord transection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693820/ https://www.ncbi.nlm.nih.gov/pubmed/23818782 http://dx.doi.org/10.2147/IJN.S44238 |
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