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Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles

Repurposing FDA-approved drugs is an efficient and cost-effective approach in the development of therapeutics for a broad range of diseases. However, prediction of function can be challenging, especially in the brain. We screened a small-molecule library with FDA-approved drugs for effects on behavi...

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Autores principales: Tucker Edmister, Sara, Del Rosario Hernández, Thaís, Ibrahim, Rahma, Brown, Cameron A., Gore, Sayali V., Kakodkar, Rohit, Kreiling, Jill A., Creton, Robbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023506/
https://www.ncbi.nlm.nih.gov/pubmed/35449173
http://dx.doi.org/10.1038/s41598-022-10133-y
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author Tucker Edmister, Sara
Del Rosario Hernández, Thaís
Ibrahim, Rahma
Brown, Cameron A.
Gore, Sayali V.
Kakodkar, Rohit
Kreiling, Jill A.
Creton, Robbert
author_facet Tucker Edmister, Sara
Del Rosario Hernández, Thaís
Ibrahim, Rahma
Brown, Cameron A.
Gore, Sayali V.
Kakodkar, Rohit
Kreiling, Jill A.
Creton, Robbert
author_sort Tucker Edmister, Sara
collection PubMed
description Repurposing FDA-approved drugs is an efficient and cost-effective approach in the development of therapeutics for a broad range of diseases. However, prediction of function can be challenging, especially in the brain. We screened a small-molecule library with FDA-approved drugs for effects on behavior. The studies were carried out using zebrafish larvae, imaged in a 384-well format. We found that various drugs affect activity, habituation, startle responses, excitability, and optomotor responses. The changes in behavior were organized in behavioral profiles, which were examined by hierarchical cluster analysis. One of the identified clusters includes the calcineurin inhibitors cyclosporine (CsA) and tacrolimus (FK506), which are immunosuppressants and potential therapeutics in the prevention of Alzheimer’s disease. The calcineurin inhibitors form a functional cluster with seemingly unrelated drugs, including bromocriptine, tetrabenazine, rosiglitazone, nebivolol, sorafenib, cabozantinib, tamoxifen, meclizine, and salmeterol. We propose that drugs with ‘CsA-type’ behavioral profiles are promising candidates for the prevention and treatment of Alzheimer’s disease.
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spelling pubmed-90235062022-04-25 Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles Tucker Edmister, Sara Del Rosario Hernández, Thaís Ibrahim, Rahma Brown, Cameron A. Gore, Sayali V. Kakodkar, Rohit Kreiling, Jill A. Creton, Robbert Sci Rep Article Repurposing FDA-approved drugs is an efficient and cost-effective approach in the development of therapeutics for a broad range of diseases. However, prediction of function can be challenging, especially in the brain. We screened a small-molecule library with FDA-approved drugs for effects on behavior. The studies were carried out using zebrafish larvae, imaged in a 384-well format. We found that various drugs affect activity, habituation, startle responses, excitability, and optomotor responses. The changes in behavior were organized in behavioral profiles, which were examined by hierarchical cluster analysis. One of the identified clusters includes the calcineurin inhibitors cyclosporine (CsA) and tacrolimus (FK506), which are immunosuppressants and potential therapeutics in the prevention of Alzheimer’s disease. The calcineurin inhibitors form a functional cluster with seemingly unrelated drugs, including bromocriptine, tetrabenazine, rosiglitazone, nebivolol, sorafenib, cabozantinib, tamoxifen, meclizine, and salmeterol. We propose that drugs with ‘CsA-type’ behavioral profiles are promising candidates for the prevention and treatment of Alzheimer’s disease. Nature Publishing Group UK 2022-04-21 /pmc/articles/PMC9023506/ /pubmed/35449173 http://dx.doi.org/10.1038/s41598-022-10133-y Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tucker Edmister, Sara
Del Rosario Hernández, Thaís
Ibrahim, Rahma
Brown, Cameron A.
Gore, Sayali V.
Kakodkar, Rohit
Kreiling, Jill A.
Creton, Robbert
Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title_full Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title_fullStr Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title_full_unstemmed Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title_short Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles
title_sort novel use of fda-approved drugs identified by cluster analysis of behavioral profiles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023506/
https://www.ncbi.nlm.nih.gov/pubmed/35449173
http://dx.doi.org/10.1038/s41598-022-10133-y
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