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Neuronal α(2)δ proteins and brain disorders
α(2)δ proteins are membrane-anchored extracellular glycoproteins which are abundantly expressed in the brain and the peripheral nervous system. They serve as regulatory subunits of voltage-gated calcium channels and, particularly in nerve cells, regulate presynaptic and postsynaptic functions indepe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351808/ https://www.ncbi.nlm.nih.gov/pubmed/32607809 http://dx.doi.org/10.1007/s00424-020-02420-2 |
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author | Ablinger, Cornelia Geisler, Stefanie M. Stanika, Ruslan I. Klein, Christian T. Obermair, Gerald J. |
author_facet | Ablinger, Cornelia Geisler, Stefanie M. Stanika, Ruslan I. Klein, Christian T. Obermair, Gerald J. |
author_sort | Ablinger, Cornelia |
collection | PubMed |
description | α(2)δ proteins are membrane-anchored extracellular glycoproteins which are abundantly expressed in the brain and the peripheral nervous system. They serve as regulatory subunits of voltage-gated calcium channels and, particularly in nerve cells, regulate presynaptic and postsynaptic functions independently from their role as channel subunits. α(2)δ proteins are the targets of the widely prescribed anti-epileptic and anti-allodynic drugs gabapentin and pregabalin, particularly for the treatment of neuropathic pain conditions. Recently, the human genes (CACNA2D1–4) encoding for the four known α(2)δ proteins (isoforms α(2)δ-1 to α(2)δ-4) have been linked to a large variety of neurological and neuropsychiatric disorders including epilepsy, autism spectrum disorders, bipolar disorders, schizophrenia, and depressive disorders. Here, we provide an overview of the hitherto identified disease associations of all known α(2)δ genes, hypothesize on the pathophysiological mechanisms considering their known physiological roles, and discuss the most immanent future research questions. Elucidating their specific physiological and pathophysiological mechanisms may open the way for developing entirely novel therapeutic paradigms for treating brain disorders. |
format | Online Article Text |
id | pubmed-7351808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-73518082020-07-16 Neuronal α(2)δ proteins and brain disorders Ablinger, Cornelia Geisler, Stefanie M. Stanika, Ruslan I. Klein, Christian T. Obermair, Gerald J. Pflugers Arch Invited Review α(2)δ proteins are membrane-anchored extracellular glycoproteins which are abundantly expressed in the brain and the peripheral nervous system. They serve as regulatory subunits of voltage-gated calcium channels and, particularly in nerve cells, regulate presynaptic and postsynaptic functions independently from their role as channel subunits. α(2)δ proteins are the targets of the widely prescribed anti-epileptic and anti-allodynic drugs gabapentin and pregabalin, particularly for the treatment of neuropathic pain conditions. Recently, the human genes (CACNA2D1–4) encoding for the four known α(2)δ proteins (isoforms α(2)δ-1 to α(2)δ-4) have been linked to a large variety of neurological and neuropsychiatric disorders including epilepsy, autism spectrum disorders, bipolar disorders, schizophrenia, and depressive disorders. Here, we provide an overview of the hitherto identified disease associations of all known α(2)δ genes, hypothesize on the pathophysiological mechanisms considering their known physiological roles, and discuss the most immanent future research questions. Elucidating their specific physiological and pathophysiological mechanisms may open the way for developing entirely novel therapeutic paradigms for treating brain disorders. Springer Berlin Heidelberg 2020-06-30 2020 /pmc/articles/PMC7351808/ /pubmed/32607809 http://dx.doi.org/10.1007/s00424-020-02420-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Invited Review Ablinger, Cornelia Geisler, Stefanie M. Stanika, Ruslan I. Klein, Christian T. Obermair, Gerald J. Neuronal α(2)δ proteins and brain disorders |
title | Neuronal α(2)δ proteins and brain disorders |
title_full | Neuronal α(2)δ proteins and brain disorders |
title_fullStr | Neuronal α(2)δ proteins and brain disorders |
title_full_unstemmed | Neuronal α(2)δ proteins and brain disorders |
title_short | Neuronal α(2)δ proteins and brain disorders |
title_sort | neuronal α(2)δ proteins and brain disorders |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351808/ https://www.ncbi.nlm.nih.gov/pubmed/32607809 http://dx.doi.org/10.1007/s00424-020-02420-2 |
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