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Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders
The sigma-1 receptor is a 223 amino acid-long protein with a recently identified structure. The sigma-2 receptor is a genetically unrelated protein with a similarly shaped binding pocket and acts to influence cellular activities similar to the sigma-1 receptor. Both proteins are highly expressed in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173947/ https://www.ncbi.nlm.nih.gov/pubmed/37166702 http://dx.doi.org/10.1007/s40263-023-01007-6 |
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author | Malar, Dicson S. Thitilertdecha, Premrutai Ruckvongacheep, Kanokphorn S. Brimson, Sirikalaya Tencomnao, Tewin Brimson, James M. |
author_facet | Malar, Dicson S. Thitilertdecha, Premrutai Ruckvongacheep, Kanokphorn S. Brimson, Sirikalaya Tencomnao, Tewin Brimson, James M. |
author_sort | Malar, Dicson S. |
collection | PubMed |
description | The sigma-1 receptor is a 223 amino acid-long protein with a recently identified structure. The sigma-2 receptor is a genetically unrelated protein with a similarly shaped binding pocket and acts to influence cellular activities similar to the sigma-1 receptor. Both proteins are highly expressed in neuronal tissues. As such, they have become targets for treating neurological diseases, including Alzheimer’s disease (AD), Huntington’s disease (HD), Parkinson’s disease (PD), multiple sclerosis (MS), Rett syndrome (RS), developmental and epileptic encephalopathies (DEE), and motor neuron disease/amyotrophic lateral sclerosis (MND/ALS). In recent years, there have been many pre-clinical and clinical studies of sigma receptor (1 and 2) ligands for treating neurological disease. Drugs such as blarcamesine, dextromethorphan and pridopidine, which have sigma-1 receptor activity as part of their pharmacological profile, are effective in treating multiple aspects of several neurological diseases. Furthermore, several sigma-2 receptor ligands are under investigation, including CT1812, rivastigmine and SAS0132. This review aims to provide a current and up-to-date analysis of the current clinical and pre-clinical data of drugs with sigma receptor activities for treating neurological disease. |
format | Online Article Text |
id | pubmed-10173947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-101739472023-05-14 Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders Malar, Dicson S. Thitilertdecha, Premrutai Ruckvongacheep, Kanokphorn S. Brimson, Sirikalaya Tencomnao, Tewin Brimson, James M. CNS Drugs Review Article The sigma-1 receptor is a 223 amino acid-long protein with a recently identified structure. The sigma-2 receptor is a genetically unrelated protein with a similarly shaped binding pocket and acts to influence cellular activities similar to the sigma-1 receptor. Both proteins are highly expressed in neuronal tissues. As such, they have become targets for treating neurological diseases, including Alzheimer’s disease (AD), Huntington’s disease (HD), Parkinson’s disease (PD), multiple sclerosis (MS), Rett syndrome (RS), developmental and epileptic encephalopathies (DEE), and motor neuron disease/amyotrophic lateral sclerosis (MND/ALS). In recent years, there have been many pre-clinical and clinical studies of sigma receptor (1 and 2) ligands for treating neurological disease. Drugs such as blarcamesine, dextromethorphan and pridopidine, which have sigma-1 receptor activity as part of their pharmacological profile, are effective in treating multiple aspects of several neurological diseases. Furthermore, several sigma-2 receptor ligands are under investigation, including CT1812, rivastigmine and SAS0132. This review aims to provide a current and up-to-date analysis of the current clinical and pre-clinical data of drugs with sigma receptor activities for treating neurological disease. Springer International Publishing 2023-05-11 2023 /pmc/articles/PMC10173947/ /pubmed/37166702 http://dx.doi.org/10.1007/s40263-023-01007-6 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Malar, Dicson S. Thitilertdecha, Premrutai Ruckvongacheep, Kanokphorn S. Brimson, Sirikalaya Tencomnao, Tewin Brimson, James M. Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title | Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title_full | Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title_fullStr | Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title_full_unstemmed | Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title_short | Targeting Sigma Receptors for the Treatment of Neurodegenerative and Neurodevelopmental Disorders |
title_sort | targeting sigma receptors for the treatment of neurodegenerative and neurodevelopmental disorders |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173947/ https://www.ncbi.nlm.nih.gov/pubmed/37166702 http://dx.doi.org/10.1007/s40263-023-01007-6 |
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