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Fishing for causes and cures of motor neuron disorders
Motor neuron disorders (MNDs) are a clinically heterogeneous group of neurological diseases characterized by progressive degeneration of motor neurons, and share some common pathological pathways. Despite remarkable advances in our understanding of these diseases, no curative treatment for MNDs exis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Limited
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073270/ https://www.ncbi.nlm.nih.gov/pubmed/24973750 http://dx.doi.org/10.1242/dmm.015719 |
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author | Patten, Shunmoogum A. Armstrong, Gary A. B. Lissouba, Alexandra Kabashi, Edor Parker, J. Alex Drapeau, Pierre |
author_facet | Patten, Shunmoogum A. Armstrong, Gary A. B. Lissouba, Alexandra Kabashi, Edor Parker, J. Alex Drapeau, Pierre |
author_sort | Patten, Shunmoogum A. |
collection | PubMed |
description | Motor neuron disorders (MNDs) are a clinically heterogeneous group of neurological diseases characterized by progressive degeneration of motor neurons, and share some common pathological pathways. Despite remarkable advances in our understanding of these diseases, no curative treatment for MNDs exists. To better understand the pathogenesis of MNDs and to help develop new treatments, the establishment of animal models that can be studied efficiently and thoroughly is paramount. The zebrafish (Danio rerio) is increasingly becoming a valuable model for studying human diseases and in screening for potential therapeutics. In this Review, we highlight recent progress in using zebrafish to study the pathology of the most common MNDs: spinal muscular atrophy (SMA), amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia (HSP). These studies indicate the power of zebrafish as a model to study the consequences of disease-related genes, because zebrafish homologues of human genes have conserved functions with respect to the aetiology of MNDs. Zebrafish also complement other animal models for the study of pathological mechanisms of MNDs and are particularly advantageous for the screening of compounds with therapeutic potential. We present an overview of their potential usefulness in MND drug discovery, which is just beginning and holds much promise for future therapeutic development. |
format | Online Article Text |
id | pubmed-4073270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Company of Biologists Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-40732702014-07-17 Fishing for causes and cures of motor neuron disorders Patten, Shunmoogum A. Armstrong, Gary A. B. Lissouba, Alexandra Kabashi, Edor Parker, J. Alex Drapeau, Pierre Dis Model Mech Review Motor neuron disorders (MNDs) are a clinically heterogeneous group of neurological diseases characterized by progressive degeneration of motor neurons, and share some common pathological pathways. Despite remarkable advances in our understanding of these diseases, no curative treatment for MNDs exists. To better understand the pathogenesis of MNDs and to help develop new treatments, the establishment of animal models that can be studied efficiently and thoroughly is paramount. The zebrafish (Danio rerio) is increasingly becoming a valuable model for studying human diseases and in screening for potential therapeutics. In this Review, we highlight recent progress in using zebrafish to study the pathology of the most common MNDs: spinal muscular atrophy (SMA), amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia (HSP). These studies indicate the power of zebrafish as a model to study the consequences of disease-related genes, because zebrafish homologues of human genes have conserved functions with respect to the aetiology of MNDs. Zebrafish also complement other animal models for the study of pathological mechanisms of MNDs and are particularly advantageous for the screening of compounds with therapeutic potential. We present an overview of their potential usefulness in MND drug discovery, which is just beginning and holds much promise for future therapeutic development. The Company of Biologists Limited 2014-07 /pmc/articles/PMC4073270/ /pubmed/24973750 http://dx.doi.org/10.1242/dmm.015719 Text en © 2014. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Patten, Shunmoogum A. Armstrong, Gary A. B. Lissouba, Alexandra Kabashi, Edor Parker, J. Alex Drapeau, Pierre Fishing for causes and cures of motor neuron disorders |
title | Fishing for causes and cures of motor neuron disorders |
title_full | Fishing for causes and cures of motor neuron disorders |
title_fullStr | Fishing for causes and cures of motor neuron disorders |
title_full_unstemmed | Fishing for causes and cures of motor neuron disorders |
title_short | Fishing for causes and cures of motor neuron disorders |
title_sort | fishing for causes and cures of motor neuron disorders |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073270/ https://www.ncbi.nlm.nih.gov/pubmed/24973750 http://dx.doi.org/10.1242/dmm.015719 |
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