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Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs

In mammals, pain is regulated by the combination of an ascending stimulating and descending inhibitory pain pathway. It remains an intriguing question whether such pain pathways are of ancient origin and conserved in invertebrates. Here we report a new Drosophila pain model and use it to elucidate t...

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Autores principales: Jang, Wijeong, Oh, Myungsok, Cho, Eun-Hee, Baek, Minwoo, Kim, Changsoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934396/
https://www.ncbi.nlm.nih.gov/pubmed/36795675
http://dx.doi.org/10.1371/journal.pone.0281874
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author Jang, Wijeong
Oh, Myungsok
Cho, Eun-Hee
Baek, Minwoo
Kim, Changsoo
author_facet Jang, Wijeong
Oh, Myungsok
Cho, Eun-Hee
Baek, Minwoo
Kim, Changsoo
author_sort Jang, Wijeong
collection PubMed
description In mammals, pain is regulated by the combination of an ascending stimulating and descending inhibitory pain pathway. It remains an intriguing question whether such pain pathways are of ancient origin and conserved in invertebrates. Here we report a new Drosophila pain model and use it to elucidate the pain pathways present in flies. The model employs transgenic flies expressing the human capsaicin receptor TRPV1 in sensory nociceptor neurons, which innervate the whole fly body, including the mouth. Upon capsaicin sipping, the flies abruptly displayed pain-related behaviors such as running away, scurrying around, rubbing vigorously, and pulling at their mouth parts, suggesting that capsaicin stimulated nociceptors in the mouth via activating TRPV1. When reared on capsaicin-containing food, the animals died of starvation, demonstrating the degree of pain experienced. This death rate was reduced by treatment both with NSAIDs and gabapentin, analgesics that inhibit the sensitized ascending pain pathway, and with antidepressants, GABAergic agonists, and morphine, analgesics that strengthen the descending inhibitory pathway. Our results suggest Drosophila to possess intricate pain sensitization and modulation mechanisms similar to mammals, and we propose that this simple, non-invasive feeding assay has utility for high-throughput evaluation and screening of analgesic compounds.
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spelling pubmed-99343962023-02-17 Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs Jang, Wijeong Oh, Myungsok Cho, Eun-Hee Baek, Minwoo Kim, Changsoo PLoS One Research Article In mammals, pain is regulated by the combination of an ascending stimulating and descending inhibitory pain pathway. It remains an intriguing question whether such pain pathways are of ancient origin and conserved in invertebrates. Here we report a new Drosophila pain model and use it to elucidate the pain pathways present in flies. The model employs transgenic flies expressing the human capsaicin receptor TRPV1 in sensory nociceptor neurons, which innervate the whole fly body, including the mouth. Upon capsaicin sipping, the flies abruptly displayed pain-related behaviors such as running away, scurrying around, rubbing vigorously, and pulling at their mouth parts, suggesting that capsaicin stimulated nociceptors in the mouth via activating TRPV1. When reared on capsaicin-containing food, the animals died of starvation, demonstrating the degree of pain experienced. This death rate was reduced by treatment both with NSAIDs and gabapentin, analgesics that inhibit the sensitized ascending pain pathway, and with antidepressants, GABAergic agonists, and morphine, analgesics that strengthen the descending inhibitory pathway. Our results suggest Drosophila to possess intricate pain sensitization and modulation mechanisms similar to mammals, and we propose that this simple, non-invasive feeding assay has utility for high-throughput evaluation and screening of analgesic compounds. Public Library of Science 2023-02-16 /pmc/articles/PMC9934396/ /pubmed/36795675 http://dx.doi.org/10.1371/journal.pone.0281874 Text en © 2023 Jang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jang, Wijeong
Oh, Myungsok
Cho, Eun-Hee
Baek, Minwoo
Kim, Changsoo
Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title_full Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title_fullStr Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title_full_unstemmed Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title_short Drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
title_sort drosophila pain sensitization and modulation unveiled by a novel pain model and analgesic drugs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934396/
https://www.ncbi.nlm.nih.gov/pubmed/36795675
http://dx.doi.org/10.1371/journal.pone.0281874
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