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Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila

There has been disagreement over the functional roles of the painless gene product in the detection and subsequent behavioral aversion to the active ingredient in wasabi, allyl isothiocyanate (AITC). Originally, painless was reported to eliminate the behavioral aversion to AITC, although subsequent...

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Autores principales: Mandel, Samantha J., Shoaf, Madison L., Braco, Jason T., Silver, Wayne L., Johnson, Erik C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038230/
https://www.ncbi.nlm.nih.gov/pubmed/30018539
http://dx.doi.org/10.3389/fncir.2018.00045
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author Mandel, Samantha J.
Shoaf, Madison L.
Braco, Jason T.
Silver, Wayne L.
Johnson, Erik C.
author_facet Mandel, Samantha J.
Shoaf, Madison L.
Braco, Jason T.
Silver, Wayne L.
Johnson, Erik C.
author_sort Mandel, Samantha J.
collection PubMed
description There has been disagreement over the functional roles of the painless gene product in the detection and subsequent behavioral aversion to the active ingredient in wasabi, allyl isothiocyanate (AITC). Originally, painless was reported to eliminate the behavioral aversion to AITC, although subsequent reports suggested that another trpA homolog, dTRPA1, was responsible for AITC aversion. We re-evaluated the role of the painless gene in the detection of AITC, employing several different behavioral assays. Using the proboscis extension reflex (PER) assay, we observed that AITC did not reduce PER frequencies in painless or dTRPA1 mutants but did in wild-type genotypes. Quantification of food intake showed a significant decline in food consumption in the presence of AITC in wild-type, but not painless mutants. We adapted an oviposition choice assay and found wild-type oviposit on substrates lacking AITC, in contrast to painless and dTRPA1 mutants. Lastly, tracking individual flies relative to a point source of AITC, showed a consistent clustering of wild-type animals away from the point source, which was absent in painless mutants. We evaluated expression patterns of both dTRPA1 and painless, which showed expression in distinct central and peripheral populations. We identified the transmitter phenotypes of subsets of painless and dTRPA1 neurons and found similar neuropeptides as those expressed by mammalian trpA expressing neurons. Using a calcium reporter, we observed AITC-evoked responses in both painless and dTRPA1 expressing neurons. Collectively, these results reaffirm the necessity of painless in nociceptive behaviors and suggest experiments to further resolve the molecular basis of aversion.
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spelling pubmed-60382302018-07-17 Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila Mandel, Samantha J. Shoaf, Madison L. Braco, Jason T. Silver, Wayne L. Johnson, Erik C. Front Neural Circuits Neuroscience There has been disagreement over the functional roles of the painless gene product in the detection and subsequent behavioral aversion to the active ingredient in wasabi, allyl isothiocyanate (AITC). Originally, painless was reported to eliminate the behavioral aversion to AITC, although subsequent reports suggested that another trpA homolog, dTRPA1, was responsible for AITC aversion. We re-evaluated the role of the painless gene in the detection of AITC, employing several different behavioral assays. Using the proboscis extension reflex (PER) assay, we observed that AITC did not reduce PER frequencies in painless or dTRPA1 mutants but did in wild-type genotypes. Quantification of food intake showed a significant decline in food consumption in the presence of AITC in wild-type, but not painless mutants. We adapted an oviposition choice assay and found wild-type oviposit on substrates lacking AITC, in contrast to painless and dTRPA1 mutants. Lastly, tracking individual flies relative to a point source of AITC, showed a consistent clustering of wild-type animals away from the point source, which was absent in painless mutants. We evaluated expression patterns of both dTRPA1 and painless, which showed expression in distinct central and peripheral populations. We identified the transmitter phenotypes of subsets of painless and dTRPA1 neurons and found similar neuropeptides as those expressed by mammalian trpA expressing neurons. Using a calcium reporter, we observed AITC-evoked responses in both painless and dTRPA1 expressing neurons. Collectively, these results reaffirm the necessity of painless in nociceptive behaviors and suggest experiments to further resolve the molecular basis of aversion. Frontiers Media S.A. 2018-07-03 /pmc/articles/PMC6038230/ /pubmed/30018539 http://dx.doi.org/10.3389/fncir.2018.00045 Text en Copyright © 2018 Mandel, Shoaf, Braco, Silver and Johnson. http://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
Mandel, Samantha J.
Shoaf, Madison L.
Braco, Jason T.
Silver, Wayne L.
Johnson, Erik C.
Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title_full Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title_fullStr Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title_full_unstemmed Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title_short Behavioral Aversion to AITC Requires Both Painless and dTRPA1 in Drosophila
title_sort behavioral aversion to aitc requires both painless and dtrpa1 in drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038230/
https://www.ncbi.nlm.nih.gov/pubmed/30018539
http://dx.doi.org/10.3389/fncir.2018.00045
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