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Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis
We provide an overview of rehabilitation in neurological diseases. A large amount of literature available on neurorehabilitation is based from the rehabilitative work on stroke and spinal cord injuries. After a brief description of rehabilitation, the potential application of neurorehabilitation in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006625/ https://www.ncbi.nlm.nih.gov/pubmed/27595123 http://dx.doi.org/10.4172/2329-9096.1000348 |
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author | Dasari, Harika Wootla, Bharath Warrington, Arthur E Rodriguez, Moses |
author_facet | Dasari, Harika Wootla, Bharath Warrington, Arthur E Rodriguez, Moses |
author_sort | Dasari, Harika |
collection | PubMed |
description | We provide an overview of rehabilitation in neurological diseases. A large amount of literature available on neurorehabilitation is based from the rehabilitative work on stroke and spinal cord injuries. After a brief description of rehabilitation, the potential application of neurorehabilitation in neurodegenerative diseases specifically multiple sclerosis (MS) is summarized. Since MS causes a wide variety of symptoms, the rehabilitation in MS patients may benefit from an interdisciplinary approach that encloses physiotherapy, cognitive rehabilitation, psychological therapy, occupational therapy, and other methods to improve fatigue. Neurorehabilitation helps patients to reach and maintain their optimal physical, psychological and intellectual, levels but it does not reverse long-term disabilities that arise from neurological disorders. This calls for the need of better neuroregenerative and neuroprotective treatment strategies in addition to neurorehabilitation. We discuss neuroprotective drugs aimed at preventing axonal, neuronal, myelin and oligodendrocyte damage and cell death that are approved and others that are currently in clinical trials, with an emphasis on human derived natural antibodies with remyleination potential. Our investigative group developed recombinant natural human IgM antibodies against oligodendrocytes and neurons with a potential for CNS repair and remyleination. One such recombinant antibody, rHIgM22 completed a phase 1 clinical trial with no toxicity and with an objective of promoting remyleination in multiple sclerosis. Inclusion of these drugs as a multifaceted approach may further enhance the efficacy of neurorehabilitation in neuroinflammatory and neurodegenerative disorders. |
format | Online Article Text |
id | pubmed-5006625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50066252016-08-31 Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis Dasari, Harika Wootla, Bharath Warrington, Arthur E Rodriguez, Moses Int J Phys Med Rehabil Article We provide an overview of rehabilitation in neurological diseases. A large amount of literature available on neurorehabilitation is based from the rehabilitative work on stroke and spinal cord injuries. After a brief description of rehabilitation, the potential application of neurorehabilitation in neurodegenerative diseases specifically multiple sclerosis (MS) is summarized. Since MS causes a wide variety of symptoms, the rehabilitation in MS patients may benefit from an interdisciplinary approach that encloses physiotherapy, cognitive rehabilitation, psychological therapy, occupational therapy, and other methods to improve fatigue. Neurorehabilitation helps patients to reach and maintain their optimal physical, psychological and intellectual, levels but it does not reverse long-term disabilities that arise from neurological disorders. This calls for the need of better neuroregenerative and neuroprotective treatment strategies in addition to neurorehabilitation. We discuss neuroprotective drugs aimed at preventing axonal, neuronal, myelin and oligodendrocyte damage and cell death that are approved and others that are currently in clinical trials, with an emphasis on human derived natural antibodies with remyleination potential. Our investigative group developed recombinant natural human IgM antibodies against oligodendrocytes and neurons with a potential for CNS repair and remyleination. One such recombinant antibody, rHIgM22 completed a phase 1 clinical trial with no toxicity and with an objective of promoting remyleination in multiple sclerosis. Inclusion of these drugs as a multifaceted approach may further enhance the efficacy of neurorehabilitation in neuroinflammatory and neurodegenerative disorders. 2016-06-23 2016-08 /pmc/articles/PMC5006625/ /pubmed/27595123 http://dx.doi.org/10.4172/2329-9096.1000348 Text en http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Dasari, Harika Wootla, Bharath Warrington, Arthur E Rodriguez, Moses Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title | Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title_full | Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title_fullStr | Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title_full_unstemmed | Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title_short | Concomitant Use of Neuroprotective Drugs in Neuro Rehabilitation of Multiple Sclerosis |
title_sort | concomitant use of neuroprotective drugs in neuro rehabilitation of multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006625/ https://www.ncbi.nlm.nih.gov/pubmed/27595123 http://dx.doi.org/10.4172/2329-9096.1000348 |
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