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Planarian nociception: Lessons from a scrunching flatworm

In addition to being studied for their exceptional regeneration abilities, planarians (i.e., flatworms) have also been extensively used in the context of pharmacological experiments during the past century. Many researchers used planarians as a model system for the study of drug abuse because they d...

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Autores principales: Reho, Guillaume, Lelièvre, Vincent, Cadiou, Hervé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362985/
https://www.ncbi.nlm.nih.gov/pubmed/35959107
http://dx.doi.org/10.3389/fnmol.2022.935918
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author Reho, Guillaume
Lelièvre, Vincent
Cadiou, Hervé
author_facet Reho, Guillaume
Lelièvre, Vincent
Cadiou, Hervé
author_sort Reho, Guillaume
collection PubMed
description In addition to being studied for their exceptional regeneration abilities, planarians (i.e., flatworms) have also been extensively used in the context of pharmacological experiments during the past century. Many researchers used planarians as a model system for the study of drug abuse because they display high similarities with the nervous system of vertebrates at cellular and molecular levels (e.g., neuronal morphology, neurotransmitter ligands, and receptor function). This research field recently led to the discovery of causal relationships between the expression of Transient Receptor Potential ion channels in planarians and their behavioral responses to noxious stimuli such as heat, cold or pharmacological analogs such as TRP agonists, among others. It has also been shown that some antinociceptive drugs modulate these behaviors. However, among the few authors that tried to implement a full behavior analysis, none reached a consensual use of the terms used to describe planarian gaits yet, nor did they establish a comprehensive description of a potential planarian nociceptive system. The aim of this review is therefore to aggregate the ancient and the most recent evidence for a true nociceptive behavior in planarians. It also highlights the convenience and relevance of this invertebrate model for nociceptive tests and suggests further lines of research. In regards to past pharmacological studies, this review finally discusses the opportunities given by the model to extensively screen for novel antinociceptive drugs.
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spelling pubmed-93629852022-08-10 Planarian nociception: Lessons from a scrunching flatworm Reho, Guillaume Lelièvre, Vincent Cadiou, Hervé Front Mol Neurosci Neuroscience In addition to being studied for their exceptional regeneration abilities, planarians (i.e., flatworms) have also been extensively used in the context of pharmacological experiments during the past century. Many researchers used planarians as a model system for the study of drug abuse because they display high similarities with the nervous system of vertebrates at cellular and molecular levels (e.g., neuronal morphology, neurotransmitter ligands, and receptor function). This research field recently led to the discovery of causal relationships between the expression of Transient Receptor Potential ion channels in planarians and their behavioral responses to noxious stimuli such as heat, cold or pharmacological analogs such as TRP agonists, among others. It has also been shown that some antinociceptive drugs modulate these behaviors. However, among the few authors that tried to implement a full behavior analysis, none reached a consensual use of the terms used to describe planarian gaits yet, nor did they establish a comprehensive description of a potential planarian nociceptive system. The aim of this review is therefore to aggregate the ancient and the most recent evidence for a true nociceptive behavior in planarians. It also highlights the convenience and relevance of this invertebrate model for nociceptive tests and suggests further lines of research. In regards to past pharmacological studies, this review finally discusses the opportunities given by the model to extensively screen for novel antinociceptive drugs. Frontiers Media S.A. 2022-07-26 /pmc/articles/PMC9362985/ /pubmed/35959107 http://dx.doi.org/10.3389/fnmol.2022.935918 Text en Copyright © 2022 Reho, Lelièvre and Cadiou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Reho, Guillaume
Lelièvre, Vincent
Cadiou, Hervé
Planarian nociception: Lessons from a scrunching flatworm
title Planarian nociception: Lessons from a scrunching flatworm
title_full Planarian nociception: Lessons from a scrunching flatworm
title_fullStr Planarian nociception: Lessons from a scrunching flatworm
title_full_unstemmed Planarian nociception: Lessons from a scrunching flatworm
title_short Planarian nociception: Lessons from a scrunching flatworm
title_sort planarian nociception: lessons from a scrunching flatworm
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362985/
https://www.ncbi.nlm.nih.gov/pubmed/35959107
http://dx.doi.org/10.3389/fnmol.2022.935918
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