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Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity
We report the evaluation of 265 compounds from a PDE-focused library for their antischistosomal activity, assessed in vitro using Schistosoma mansoni. Of the tested compounds, 171 (64%) displayed selective in vitro activity, with 16 causing worm hypermotility/spastic contractions and 41 inducing var...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350229/ https://www.ncbi.nlm.nih.gov/pubmed/30669086 http://dx.doi.org/10.1016/j.ijpddr.2019.01.001 |
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author | Botros, Sanaa S. William, Samia Sabra, Abdel-Nasser A. El-Lakkany, Naglaa M. Seif el-Din, Sayed H. García-Rubia, Alfonso Sebastián-Pérez, Victor Blaazer, Antoni R. de Heuvel, Erik Sijm, Maarten Zheng, Yang Salado, Irene G. Munday, Jane C. Maes, Louis de Esch, Iwan J.P. Sterk, Geert J. Augustyns, Koen Leurs, Rob Gil, Carmen De Koning, Harry P. |
author_facet | Botros, Sanaa S. William, Samia Sabra, Abdel-Nasser A. El-Lakkany, Naglaa M. Seif el-Din, Sayed H. García-Rubia, Alfonso Sebastián-Pérez, Victor Blaazer, Antoni R. de Heuvel, Erik Sijm, Maarten Zheng, Yang Salado, Irene G. Munday, Jane C. Maes, Louis de Esch, Iwan J.P. Sterk, Geert J. Augustyns, Koen Leurs, Rob Gil, Carmen De Koning, Harry P. |
author_sort | Botros, Sanaa S. |
collection | PubMed |
description | We report the evaluation of 265 compounds from a PDE-focused library for their antischistosomal activity, assessed in vitro using Schistosoma mansoni. Of the tested compounds, 171 (64%) displayed selective in vitro activity, with 16 causing worm hypermotility/spastic contractions and 41 inducing various degrees of worm killing at 100 μM, with the surviving worms displaying sluggish movement, worm unpairing and complete absence of eggs. The compounds that did not affect worm viability (n = 72) induced a complete cessation of ovipositing. 82% of the compounds had an impact on male worms whereas female worms were barely affected. In vivo evaluation in S. mansoni-infected mice with the in vitro ‘hit’ NPD-0274 at 20 mg/kg/day orally for 5 days resulted in worm burden reductions of 29% and intestinal tissue egg load reduction of 35% at 10 days post-treatment. Combination of praziquantel (PZQ) at 10 mg/kg/day for 5 days with NPD-0274 or NPD-0298 resulted in significantly higher worm killing than PZQ alone, as well as a reduction in intestinal tissue egg load, disappearance of immature eggs and an increase in the number of dead eggs. |
format | Online Article Text |
id | pubmed-6350229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63502292019-02-05 Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity Botros, Sanaa S. William, Samia Sabra, Abdel-Nasser A. El-Lakkany, Naglaa M. Seif el-Din, Sayed H. García-Rubia, Alfonso Sebastián-Pérez, Victor Blaazer, Antoni R. de Heuvel, Erik Sijm, Maarten Zheng, Yang Salado, Irene G. Munday, Jane C. Maes, Louis de Esch, Iwan J.P. Sterk, Geert J. Augustyns, Koen Leurs, Rob Gil, Carmen De Koning, Harry P. Int J Parasitol Drugs Drug Resist Article We report the evaluation of 265 compounds from a PDE-focused library for their antischistosomal activity, assessed in vitro using Schistosoma mansoni. Of the tested compounds, 171 (64%) displayed selective in vitro activity, with 16 causing worm hypermotility/spastic contractions and 41 inducing various degrees of worm killing at 100 μM, with the surviving worms displaying sluggish movement, worm unpairing and complete absence of eggs. The compounds that did not affect worm viability (n = 72) induced a complete cessation of ovipositing. 82% of the compounds had an impact on male worms whereas female worms were barely affected. In vivo evaluation in S. mansoni-infected mice with the in vitro ‘hit’ NPD-0274 at 20 mg/kg/day orally for 5 days resulted in worm burden reductions of 29% and intestinal tissue egg load reduction of 35% at 10 days post-treatment. Combination of praziquantel (PZQ) at 10 mg/kg/day for 5 days with NPD-0274 or NPD-0298 resulted in significantly higher worm killing than PZQ alone, as well as a reduction in intestinal tissue egg load, disappearance of immature eggs and an increase in the number of dead eggs. Elsevier 2019-01-14 /pmc/articles/PMC6350229/ /pubmed/30669086 http://dx.doi.org/10.1016/j.ijpddr.2019.01.001 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Botros, Sanaa S. William, Samia Sabra, Abdel-Nasser A. El-Lakkany, Naglaa M. Seif el-Din, Sayed H. García-Rubia, Alfonso Sebastián-Pérez, Victor Blaazer, Antoni R. de Heuvel, Erik Sijm, Maarten Zheng, Yang Salado, Irene G. Munday, Jane C. Maes, Louis de Esch, Iwan J.P. Sterk, Geert J. Augustyns, Koen Leurs, Rob Gil, Carmen De Koning, Harry P. Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title | Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title_full | Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title_fullStr | Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title_full_unstemmed | Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title_short | Screening of a PDE-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
title_sort | screening of a pde-focused library identifies imidazoles with in vitro and in vivo antischistosomal activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350229/ https://www.ncbi.nlm.nih.gov/pubmed/30669086 http://dx.doi.org/10.1016/j.ijpddr.2019.01.001 |
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