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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...

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Autores principales: Seeley, Aidan, Bellamy, Caitlin, Davies, Nia A., Wallace, Melisa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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