Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury

Abstract Background Evidence has suggested that human adipose-derived stem cells (hADSCs) and low-level laser has neuroprotective effects on spinal cord injury (SCI). Therefore, the combined effect of the hADSCs and laser on neuregeneration and neuropathic pain after SCI was investigated. Methods Fo...

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Main Authors: Arash Sarveazad, Atousa Janzadeh, Gholamreza Taheripak, Sima Dameni, Mahmoud Yousefifard, Farinaz Nasirinezhad
Format: Article
Language:English
Published: BMC 2019-06-01
Series:Stem Cell Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13287-019-1269-y
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author Arash Sarveazad
Atousa Janzadeh
Gholamreza Taheripak
Sima Dameni
Mahmoud Yousefifard
Farinaz Nasirinezhad
author_facet Arash Sarveazad
Atousa Janzadeh
Gholamreza Taheripak
Sima Dameni
Mahmoud Yousefifard
Farinaz Nasirinezhad
author_sort Arash Sarveazad
collection DOAJ
description Abstract Background Evidence has suggested that human adipose-derived stem cells (hADSCs) and low-level laser has neuroprotective effects on spinal cord injury (SCI). Therefore, the combined effect of the hADSCs and laser on neuregeneration and neuropathic pain after SCI was investigated. Methods Forty-eight adult male Wistar rats with 200–250 g weight were used. Thirty minutes after compression, injury with laser was irritated, and 1 week following SCI, about 1 × 106 cells were transplanted into the spinal cord. Motor function and neuropathic pain were assessed weekly. Molecular and histological studies were done at the end of the fourth week. Results The combined application of hADSCs and laser has significantly improved motor function recovery (p = 0.0001), hyperalgesia (p < 0.05), and allodynia (p < 0.05). GDNF mRNA expression was significantly increased in hADSCs and laser+hADSC-treated animals (p < 0.001). Finally, co-administration of hADSCs and laser has enhanced the number of axons around cavity more than other treatments (p < 0.001). Conclusions The results showed that the combination of laser and ADSCs could significantly improve the motor function and alleviate SCI-induced allodynia and hyperalgesia. Therefore, using a combination of laser and hADSCs in future experimental and translational clinical studies is suggested.
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spelling doaj.art-fa49bc7f5c214355b2b7dd89a89614c22022-12-22T00:17:26ZengBMCStem Cell Research & Therapy1757-65122019-06-0110111510.1186/s13287-019-1269-yCo-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injuryArash Sarveazad0Atousa Janzadeh1Gholamreza Taheripak2Sima Dameni3Mahmoud Yousefifard4Farinaz Nasirinezhad5Colorectal Research Center, Iran University of Medical SciencesRadiation Biology Research Center, Iran University of Medical SciencesDepartment of Biochemistry, Faculty of Medicine, Iran University of Medical SciencesPhysiology Research Center, Faculty of Medicine, Iran University of Medical SciencesPhysiology Research Center, Faculty of Medicine, Iran University of Medical SciencesPhysiology Research Center and Department of Physiology, Faculty of Medicine, Iran University of Medical SciencesAbstract Background Evidence has suggested that human adipose-derived stem cells (hADSCs) and low-level laser has neuroprotective effects on spinal cord injury (SCI). Therefore, the combined effect of the hADSCs and laser on neuregeneration and neuropathic pain after SCI was investigated. Methods Forty-eight adult male Wistar rats with 200–250 g weight were used. Thirty minutes after compression, injury with laser was irritated, and 1 week following SCI, about 1 × 106 cells were transplanted into the spinal cord. Motor function and neuropathic pain were assessed weekly. Molecular and histological studies were done at the end of the fourth week. Results The combined application of hADSCs and laser has significantly improved motor function recovery (p = 0.0001), hyperalgesia (p < 0.05), and allodynia (p < 0.05). GDNF mRNA expression was significantly increased in hADSCs and laser+hADSC-treated animals (p < 0.001). Finally, co-administration of hADSCs and laser has enhanced the number of axons around cavity more than other treatments (p < 0.001). Conclusions The results showed that the combination of laser and ADSCs could significantly improve the motor function and alleviate SCI-induced allodynia and hyperalgesia. Therefore, using a combination of laser and hADSCs in future experimental and translational clinical studies is suggested.http://link.springer.com/article/10.1186/s13287-019-1269-yGSK3 betaNeurodegenerationNeuropathic painHyperalgesiaAllodyniaSpinal cord injury
spellingShingle Arash Sarveazad
Atousa Janzadeh
Gholamreza Taheripak
Sima Dameni
Mahmoud Yousefifard
Farinaz Nasirinezhad
Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
Stem Cell Research & Therapy
GSK3 beta
Neurodegeneration
Neuropathic pain
Hyperalgesia
Allodynia
Spinal cord injury
title Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
title_full Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
title_fullStr Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
title_full_unstemmed Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
title_short Co-administration of human adipose-derived stem cells and low-level laser to alleviate neuropathic pain after experimental spinal cord injury
title_sort co administration of human adipose derived stem cells and low level laser to alleviate neuropathic pain after experimental spinal cord injury
topic GSK3 beta
Neurodegeneration
Neuropathic pain
Hyperalgesia
Allodynia
Spinal cord injury
url http://link.springer.com/article/10.1186/s13287-019-1269-y
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