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Current Therapy of Drugs in Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS), commonly termed as motor neuron disease (MND) in UK, is a chronically lethal disorder among the neurodegenerative diseases, meanwhile. ALS is basically irreversible and progressive deterioration of upper and lower motor neurons in the motor cortex, brain stem and...

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Autores principales: Lu, Haiyan, Le, Wei Dong, Xie, Ya-Ying, Wang, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876587/
https://www.ncbi.nlm.nih.gov/pubmed/26786249
http://dx.doi.org/10.2174/1570159X14666160120152423
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author Lu, Haiyan
Le, Wei Dong
Xie, Ya-Ying
Wang, Xiao-Ping
author_facet Lu, Haiyan
Le, Wei Dong
Xie, Ya-Ying
Wang, Xiao-Ping
author_sort Lu, Haiyan
collection PubMed
description Amyotrophic lateral sclerosis (ALS), commonly termed as motor neuron disease (MND) in UK, is a chronically lethal disorder among the neurodegenerative diseases, meanwhile. ALS is basically irreversible and progressive deterioration of upper and lower motor neurons in the motor cortex, brain stem and medulla spinalis. Riluzole, used for the treatment of ALS, was demonstrated to slightly delay the initiation of respiratory dysfunction and extend the median survival of patients by a few months. In this study, the key biochemical defects were discussed, such as: mutant Cu/Zn superoxide dismutase, mitochondrial protectants, and anti-excitotoxic/ anti-oxidative / anti-inflammatory/ anti-apoptotic agents, so the related drug candidates that have been studied in ALS models would possibly be further used in ALS patients.
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spelling pubmed-48765872016-11-01 Current Therapy of Drugs in Amyotrophic Lateral Sclerosis Lu, Haiyan Le, Wei Dong Xie, Ya-Ying Wang, Xiao-Ping Curr Neuropharmacol Article Amyotrophic lateral sclerosis (ALS), commonly termed as motor neuron disease (MND) in UK, is a chronically lethal disorder among the neurodegenerative diseases, meanwhile. ALS is basically irreversible and progressive deterioration of upper and lower motor neurons in the motor cortex, brain stem and medulla spinalis. Riluzole, used for the treatment of ALS, was demonstrated to slightly delay the initiation of respiratory dysfunction and extend the median survival of patients by a few months. In this study, the key biochemical defects were discussed, such as: mutant Cu/Zn superoxide dismutase, mitochondrial protectants, and anti-excitotoxic/ anti-oxidative / anti-inflammatory/ anti-apoptotic agents, so the related drug candidates that have been studied in ALS models would possibly be further used in ALS patients. Bentham Science Publishers 2016-05 2016-05 /pmc/articles/PMC4876587/ /pubmed/26786249 http://dx.doi.org/10.2174/1570159X14666160120152423 Text en ©2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Lu, Haiyan
Le, Wei Dong
Xie, Ya-Ying
Wang, Xiao-Ping
Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title_full Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title_fullStr Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title_full_unstemmed Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title_short Current Therapy of Drugs in Amyotrophic Lateral Sclerosis
title_sort current therapy of drugs in amyotrophic lateral sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876587/
https://www.ncbi.nlm.nih.gov/pubmed/26786249
http://dx.doi.org/10.2174/1570159X14666160120152423
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