1. Academic Validation
  2. Novel use of FDA-approved drugs identified by cluster analysis of behavioral profiles

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

  • Sci Rep. 2022 Apr 21;12(1):6120. doi: 10.1038/s41598-022-10133-y.
Sara Tucker Edmister 1 Thaís Del Rosario Hernández 1 Rahma Ibrahim 1 Cameron A Brown 1 Sayali V Gore 1 Rohit Kakodkar 2 Jill A Kreiling 1 Robbert Creton 3
Affiliations

Affiliations

  • 1 Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island, USA.
  • 2 Center for Computation and Visualization, Brown University, Providence, Rhode Island, USA.
  • 3 Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island, USA. [email protected].
Abstract

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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