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Lumbriculus variegatus: A novel organism for in vivo pharmacology education
Pharmacology graduates require an understanding of both in vitro and in vivo drug responses but there has been a decline in animal use in pharmacology education over the last 30 years. To address this, we present the novel invertebrate model, Lumbriculus variegatus, for in vivo testing of drugs in a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380063/ https://www.ncbi.nlm.nih.gov/pubmed/34415088 http://dx.doi.org/10.1002/prp2.853 |
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author | Seeley, Aidan Bellamy, Caitlin Davies, Nia A. Wallace, Melisa J. |
author_facet | Seeley, Aidan Bellamy, Caitlin Davies, Nia A. Wallace, Melisa J. |
author_sort | Seeley, Aidan |
collection | PubMed |
description | Pharmacology graduates require an understanding of both in vitro and in vivo drug responses but there has been a decline in animal use in pharmacology education over the last 30 years. To address this, we present the novel invertebrate model, Lumbriculus variegatus, for in vivo testing of drugs in a teaching environment. We have developed two novel behavioral assays: the stereotypical movement assay, which measures the effect of drugs on the ability of L. variegatus to perform stereotypical movements following tactile stimulation, and the free locomotion assay, which measures drug effects on unstimulated movement. We report the effects of compounds with diverse pharmacodynamic properties on L. variegatus using these assays. The ryanodine receptor antagonist, dantrolene, altered the unstimulated movement of L. variegatus at 5 μM, whereas stimulated movement was inhibited at ≥25 μM. Lidocaine, a voltage‐gated sodium channel blocker, and quinine, a nonselective sodium and potassium channel blocker, reduced both stimulated and unstimulated L. variegatus movement at ≥0.5 mM. Inhibitory effects of quinine persisted for up to 24 h after drug removal, whereas lidocaine effects were reduced 10 min after drug removal. Herein, we provide proof‐of‐concept utilization of L. variegatus as an organism for use in in vivo pharmacology education but without regulatory constraints or the need for specialized equipment and training. |
format | Online Article Text |
id | pubmed-8380063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83800632021-08-27 Lumbriculus variegatus: A novel organism for in vivo pharmacology education Seeley, Aidan Bellamy, Caitlin Davies, Nia A. Wallace, Melisa J. Pharmacol Res Perspect Pharmacology Education and Innovation Series Pharmacology graduates require an understanding of both in vitro and in vivo drug responses but there has been a decline in animal use in pharmacology education over the last 30 years. To address this, we present the novel invertebrate model, Lumbriculus variegatus, for in vivo testing of drugs in a teaching environment. We have developed two novel behavioral assays: the stereotypical movement assay, which measures the effect of drugs on the ability of L. variegatus to perform stereotypical movements following tactile stimulation, and the free locomotion assay, which measures drug effects on unstimulated movement. We report the effects of compounds with diverse pharmacodynamic properties on L. variegatus using these assays. The ryanodine receptor antagonist, dantrolene, altered the unstimulated movement of L. variegatus at 5 μM, whereas stimulated movement was inhibited at ≥25 μM. Lidocaine, a voltage‐gated sodium channel blocker, and quinine, a nonselective sodium and potassium channel blocker, reduced both stimulated and unstimulated L. variegatus movement at ≥0.5 mM. Inhibitory effects of quinine persisted for up to 24 h after drug removal, whereas lidocaine effects were reduced 10 min after drug removal. Herein, we provide proof‐of‐concept utilization of L. variegatus as an organism for use in in vivo pharmacology education but without regulatory constraints or the need for specialized equipment and training. John Wiley and Sons Inc. 2021-08-20 /pmc/articles/PMC8380063/ /pubmed/34415088 http://dx.doi.org/10.1002/prp2.853 Text en © 2021 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Pharmacology Education and Innovation Series Seeley, Aidan Bellamy, Caitlin Davies, Nia A. Wallace, Melisa J. Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title | Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title_full | Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title_fullStr | Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title_full_unstemmed | Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title_short | Lumbriculus variegatus: A novel organism for in vivo pharmacology education |
title_sort | lumbriculus variegatus: a novel organism for in vivo pharmacology education |
topic | Pharmacology Education and Innovation Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380063/ https://www.ncbi.nlm.nih.gov/pubmed/34415088 http://dx.doi.org/10.1002/prp2.853 |
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