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Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate
Mutations in the glucocerebrosidase 1 (GBA1) gene are related to both Parkinson disease (PD) and Gaucher disease (GD). In both cases, the condition is associated with deficiency of glucocerebrosidase (GCase), the enzyme encoded by GBA1. Ambroxol is a small molecule chaperone that has been shown in m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485051/ https://www.ncbi.nlm.nih.gov/pubmed/28295625 http://dx.doi.org/10.1002/syn.21967 |
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author | Migdalska‐Richards, Anna Ko, Wai Kin D. Li, Qin Bezard, Erwan Schapira, Anthony H. V. |
author_facet | Migdalska‐Richards, Anna Ko, Wai Kin D. Li, Qin Bezard, Erwan Schapira, Anthony H. V. |
author_sort | Migdalska‐Richards, Anna |
collection | PubMed |
description | Mutations in the glucocerebrosidase 1 (GBA1) gene are related to both Parkinson disease (PD) and Gaucher disease (GD). In both cases, the condition is associated with deficiency of glucocerebrosidase (GCase), the enzyme encoded by GBA1. Ambroxol is a small molecule chaperone that has been shown in mice to cross the blood‐brain barrier, increase GCase activity and reduce alpha‐synuclein protein levels. In this study, we analyze the effect of ambroxol treatment on GCase activity in healthy nonhuman primates. We show that daily administration of ambroxol results in increased brain GCase activity. Our work further indicates that ambroxol should be investigated as a novel therapy for both PD and neuronopathic GD in humans. |
format | Online Article Text |
id | pubmed-5485051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54850512017-07-11 Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate Migdalska‐Richards, Anna Ko, Wai Kin D. Li, Qin Bezard, Erwan Schapira, Anthony H. V. Synapse Short Communication Mutations in the glucocerebrosidase 1 (GBA1) gene are related to both Parkinson disease (PD) and Gaucher disease (GD). In both cases, the condition is associated with deficiency of glucocerebrosidase (GCase), the enzyme encoded by GBA1. Ambroxol is a small molecule chaperone that has been shown in mice to cross the blood‐brain barrier, increase GCase activity and reduce alpha‐synuclein protein levels. In this study, we analyze the effect of ambroxol treatment on GCase activity in healthy nonhuman primates. We show that daily administration of ambroxol results in increased brain GCase activity. Our work further indicates that ambroxol should be investigated as a novel therapy for both PD and neuronopathic GD in humans. John Wiley and Sons Inc. 2017-03-17 2017-07 /pmc/articles/PMC5485051/ /pubmed/28295625 http://dx.doi.org/10.1002/syn.21967 Text en © 2017 The Authors Synapse Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Migdalska‐Richards, Anna Ko, Wai Kin D. Li, Qin Bezard, Erwan Schapira, Anthony H. V. Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title | Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title_full | Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title_fullStr | Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title_full_unstemmed | Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title_short | Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
title_sort | oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485051/ https://www.ncbi.nlm.nih.gov/pubmed/28295625 http://dx.doi.org/10.1002/syn.21967 |
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