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Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury

BACKGROUND: Spinal cord injury (SCI) leads to permanent functional deficits because the central nervous system lacks the ability for spontaneous repair. Cell therapy strategies offered a hope in neurological repair. The clinical use of human embryonic stem cell transplantation is hampered by scienti...

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Autores principales: Muniswami, Durai Murugan, Tharion, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259289/
https://www.ncbi.nlm.nih.gov/pubmed/30598908
http://dx.doi.org/10.4103/ijabmr.IJABMR_436_17
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author Muniswami, Durai Murugan
Tharion, George
author_facet Muniswami, Durai Murugan
Tharion, George
author_sort Muniswami, Durai Murugan
collection PubMed
description BACKGROUND: Spinal cord injury (SCI) leads to permanent functional deficits because the central nervous system lacks the ability for spontaneous repair. Cell therapy strategies offered a hope in neurological repair. The clinical use of human embryonic stem cell transplantation is hampered by scientific and ethical controversies. Olfactory ensheathing cells (OECs)/bone marrow mesenchymal stem cell (MSC) is a promising cell source for autologous neurotransplantation devoid of ethical concerns. AIM: This study aimed to evaluate the combined therapeutic effect of OEC, MSC, and chondroitinase in SCI rat models. MATERIALS AND METHODS: Adult female albino Wistar rats were divided into ten groups, n = 6 rats in each group and control (n = 11). T10 level laminectomy was done in anesthetized rats to create drop-weight SCI. Both OEC and MSC were transplanted on the 9(th) day following SCI as a combined therapy with different dosage of 2 × 10(5), 5 × 10(5), 10 × 10(5), and >10 × 10(5) at a ratio of 1:1 with/without chondroitinase (0.2 U). One group of SCI rats was treated with chondroitinase alone 0.2 U. Dulbecco's Modified Eagle medium was injected in control rats. The outcome of transplantation was assessed using Basso, Beattie, Bresnahan (BBB) scale and motor-evoked potential studies. RESULTS: All the treated groups showed hindlimb motor recovery in BBB score except control group (P < 0.05). All the three combinations showed better results than OEC + MSC groups in hindlimb motor recovery. In dose–response relationship, 5- and 10-lakh combinations elicited increased functional recovery than 2- and more than 10-lakh combinations. However, chondroitinase alone demonstrated a highest BBB score than any other groups. CONCLUSIONS: Chondroitinase/cell combinations have a therapeutic beneficial effect in SCI.
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spelling pubmed-62592892018-12-31 Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury Muniswami, Durai Murugan Tharion, George Int J Appl Basic Med Res Original Article BACKGROUND: Spinal cord injury (SCI) leads to permanent functional deficits because the central nervous system lacks the ability for spontaneous repair. Cell therapy strategies offered a hope in neurological repair. The clinical use of human embryonic stem cell transplantation is hampered by scientific and ethical controversies. Olfactory ensheathing cells (OECs)/bone marrow mesenchymal stem cell (MSC) is a promising cell source for autologous neurotransplantation devoid of ethical concerns. AIM: This study aimed to evaluate the combined therapeutic effect of OEC, MSC, and chondroitinase in SCI rat models. MATERIALS AND METHODS: Adult female albino Wistar rats were divided into ten groups, n = 6 rats in each group and control (n = 11). T10 level laminectomy was done in anesthetized rats to create drop-weight SCI. Both OEC and MSC were transplanted on the 9(th) day following SCI as a combined therapy with different dosage of 2 × 10(5), 5 × 10(5), 10 × 10(5), and >10 × 10(5) at a ratio of 1:1 with/without chondroitinase (0.2 U). One group of SCI rats was treated with chondroitinase alone 0.2 U. Dulbecco's Modified Eagle medium was injected in control rats. The outcome of transplantation was assessed using Basso, Beattie, Bresnahan (BBB) scale and motor-evoked potential studies. RESULTS: All the treated groups showed hindlimb motor recovery in BBB score except control group (P < 0.05). All the three combinations showed better results than OEC + MSC groups in hindlimb motor recovery. In dose–response relationship, 5- and 10-lakh combinations elicited increased functional recovery than 2- and more than 10-lakh combinations. However, chondroitinase alone demonstrated a highest BBB score than any other groups. CONCLUSIONS: Chondroitinase/cell combinations have a therapeutic beneficial effect in SCI. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6259289/ /pubmed/30598908 http://dx.doi.org/10.4103/ijabmr.IJABMR_436_17 Text en Copyright: © 2018 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Muniswami, Durai Murugan
Tharion, George
Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title_full Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title_fullStr Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title_full_unstemmed Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title_short Therapeutic Effect of Cell Transplantation and Chondroitinase in Rat Spinal Cord Injury
title_sort therapeutic effect of cell transplantation and chondroitinase in rat spinal cord injury
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259289/
https://www.ncbi.nlm.nih.gov/pubmed/30598908
http://dx.doi.org/10.4103/ijabmr.IJABMR_436_17
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