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Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease

Terazosin is an α(1)-adrenergic receptor antagonist that enhances glycolysis and increases cellular ATP by binding to the enzyme phosphoglycerate kinase 1 (PGK1). Recent work has shown that terazosin is protective against motor dysfunction in rodent models of Parkinson’s disease (PD) and is associat...

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Autores principales: Weber, Matthew A., Sivakumar, Kartik, Tabakovic, Ervina E., Oya, Mayu, Aldridge, Georgina M., Zhang, Qiang, Simmering, Jacob E., Narayanan, Nandakumar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981768/
https://www.ncbi.nlm.nih.gov/pubmed/36864060
http://dx.doi.org/10.1038/s41531-023-00477-1
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author Weber, Matthew A.
Sivakumar, Kartik
Tabakovic, Ervina E.
Oya, Mayu
Aldridge, Georgina M.
Zhang, Qiang
Simmering, Jacob E.
Narayanan, Nandakumar S.
author_facet Weber, Matthew A.
Sivakumar, Kartik
Tabakovic, Ervina E.
Oya, Mayu
Aldridge, Georgina M.
Zhang, Qiang
Simmering, Jacob E.
Narayanan, Nandakumar S.
author_sort Weber, Matthew A.
collection PubMed
description Terazosin is an α(1)-adrenergic receptor antagonist that enhances glycolysis and increases cellular ATP by binding to the enzyme phosphoglycerate kinase 1 (PGK1). Recent work has shown that terazosin is protective against motor dysfunction in rodent models of Parkinson’s disease (PD) and is associated with slowed motor symptom progression in PD patients. However, PD is also characterized by profound cognitive symptoms. We tested the hypothesis that terazosin protects against cognitive symptoms associated with PD. We report two main results. First, in rodents with ventral tegmental area (VTA) dopamine depletion modeling aspects of PD-related cognitive dysfunction, we found that terazosin preserved cognitive function. Second, we found that after matching for demographics, comorbidities, and disease duration, PD patients newly started on terazosin, alfuzosin, or doxazosin had a lower hazard of being diagnosed with dementia compared to tamsulosin, an α(1)-adrenergic receptor antagonist that does not enhance glycolysis. Together, these findings suggest that in addition to slowing motor symptom progression, glycolysis-enhancing drugs protect against cognitive symptoms of PD.
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spelling pubmed-99817682023-03-04 Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease Weber, Matthew A. Sivakumar, Kartik Tabakovic, Ervina E. Oya, Mayu Aldridge, Georgina M. Zhang, Qiang Simmering, Jacob E. Narayanan, Nandakumar S. NPJ Parkinsons Dis Article Terazosin is an α(1)-adrenergic receptor antagonist that enhances glycolysis and increases cellular ATP by binding to the enzyme phosphoglycerate kinase 1 (PGK1). Recent work has shown that terazosin is protective against motor dysfunction in rodent models of Parkinson’s disease (PD) and is associated with slowed motor symptom progression in PD patients. However, PD is also characterized by profound cognitive symptoms. We tested the hypothesis that terazosin protects against cognitive symptoms associated with PD. We report two main results. First, in rodents with ventral tegmental area (VTA) dopamine depletion modeling aspects of PD-related cognitive dysfunction, we found that terazosin preserved cognitive function. Second, we found that after matching for demographics, comorbidities, and disease duration, PD patients newly started on terazosin, alfuzosin, or doxazosin had a lower hazard of being diagnosed with dementia compared to tamsulosin, an α(1)-adrenergic receptor antagonist that does not enhance glycolysis. Together, these findings suggest that in addition to slowing motor symptom progression, glycolysis-enhancing drugs protect against cognitive symptoms of PD. Nature Publishing Group UK 2023-03-02 /pmc/articles/PMC9981768/ /pubmed/36864060 http://dx.doi.org/10.1038/s41531-023-00477-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Weber, Matthew A.
Sivakumar, Kartik
Tabakovic, Ervina E.
Oya, Mayu
Aldridge, Georgina M.
Zhang, Qiang
Simmering, Jacob E.
Narayanan, Nandakumar S.
Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title_full Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title_fullStr Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title_full_unstemmed Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title_short Glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease
title_sort glycolysis-enhancing α(1)-adrenergic antagonists modify cognitive symptoms related to parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981768/
https://www.ncbi.nlm.nih.gov/pubmed/36864060
http://dx.doi.org/10.1038/s41531-023-00477-1
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