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Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions
BACKGROUND: Prion-based diseases are incurable transmissible neurodegenerative disorders affecting animals and humans. METHODOLOGY/PRINCIPAL FINDINGS: Here we report the discovery of the in vivo antiprion activity of Guanabenz (GA), an agonist of α2-adrenergic receptors routinely used in human medic...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291559/ https://www.ncbi.nlm.nih.gov/pubmed/18431471 http://dx.doi.org/10.1371/journal.pone.0001981 |
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author | Tribouillard-Tanvier, Déborah Béringue, Vincent Desban, Nathalie Gug, Fabienne Bach, Stéphane Voisset, Cécile Galons, Hervé Laude, Hubert Vilette, Didier Blondel, Marc |
author_facet | Tribouillard-Tanvier, Déborah Béringue, Vincent Desban, Nathalie Gug, Fabienne Bach, Stéphane Voisset, Cécile Galons, Hervé Laude, Hubert Vilette, Didier Blondel, Marc |
author_sort | Tribouillard-Tanvier, Déborah |
collection | PubMed |
description | BACKGROUND: Prion-based diseases are incurable transmissible neurodegenerative disorders affecting animals and humans. METHODOLOGY/PRINCIPAL FINDINGS: Here we report the discovery of the in vivo antiprion activity of Guanabenz (GA), an agonist of α2-adrenergic receptors routinely used in human medicine as an antihypertensive drug. We isolated GA in a screen for drugs active in vivo against two different yeast prions using a previously described yeast-based two steps assay. GA was then shown to promote ovine PrP(Sc) clearance in a cell-based assay. These effects are very specific as evidenced by the lack of activity of some GA analogues that we generated. GA antiprion activity does not involve its agonist activity on α2-adrenergic receptors as other chemically close anti-hypertensive agents possessing related mechanism of action were found inactive against prions. Finally, GA showed activity in a transgenic mouse-based in vivo assay for ovine prion propagation, prolonging slightly but significantly the survival of treated animals. CONCLUSION/SIGNIFICANCE: GA thus adds to the short list of compounds active in vivo in animal models for the treatment of prion-based diseases. Because it has been administrated for many years to treat hypertension on a daily basis, without major side-effects, our results suggest that it could be evaluated in human as a potential treatment for prion-based diseases. |
format | Text |
id | pubmed-2291559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22915592008-04-23 Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions Tribouillard-Tanvier, Déborah Béringue, Vincent Desban, Nathalie Gug, Fabienne Bach, Stéphane Voisset, Cécile Galons, Hervé Laude, Hubert Vilette, Didier Blondel, Marc PLoS One Research Article BACKGROUND: Prion-based diseases are incurable transmissible neurodegenerative disorders affecting animals and humans. METHODOLOGY/PRINCIPAL FINDINGS: Here we report the discovery of the in vivo antiprion activity of Guanabenz (GA), an agonist of α2-adrenergic receptors routinely used in human medicine as an antihypertensive drug. We isolated GA in a screen for drugs active in vivo against two different yeast prions using a previously described yeast-based two steps assay. GA was then shown to promote ovine PrP(Sc) clearance in a cell-based assay. These effects are very specific as evidenced by the lack of activity of some GA analogues that we generated. GA antiprion activity does not involve its agonist activity on α2-adrenergic receptors as other chemically close anti-hypertensive agents possessing related mechanism of action were found inactive against prions. Finally, GA showed activity in a transgenic mouse-based in vivo assay for ovine prion propagation, prolonging slightly but significantly the survival of treated animals. CONCLUSION/SIGNIFICANCE: GA thus adds to the short list of compounds active in vivo in animal models for the treatment of prion-based diseases. Because it has been administrated for many years to treat hypertension on a daily basis, without major side-effects, our results suggest that it could be evaluated in human as a potential treatment for prion-based diseases. Public Library of Science 2008-04-23 /pmc/articles/PMC2291559/ /pubmed/18431471 http://dx.doi.org/10.1371/journal.pone.0001981 Text en Tribouillard-Tanvier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tribouillard-Tanvier, Déborah Béringue, Vincent Desban, Nathalie Gug, Fabienne Bach, Stéphane Voisset, Cécile Galons, Hervé Laude, Hubert Vilette, Didier Blondel, Marc Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title | Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title_full | Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title_fullStr | Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title_full_unstemmed | Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title_short | Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions |
title_sort | antihypertensive drug guanabenz is active in vivo against both yeast and mammalian prions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291559/ https://www.ncbi.nlm.nih.gov/pubmed/18431471 http://dx.doi.org/10.1371/journal.pone.0001981 |
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