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Crayfish Self-Administer Amphetamine in a Spatially Contingent Task

Natural reward is an essential element of any organism’s ability to adapt to environmental variation. Its underlying circuits and mechanisms guide the learning process as they help associate an event, or cue, with the perception of an outcome’s value. More generally, natural reward serves as the fun...

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Autores principales: Datta, Udita, van Staaden, Moira, Huber, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961511/
https://www.ncbi.nlm.nih.gov/pubmed/29867520
http://dx.doi.org/10.3389/fphys.2018.00433
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author Datta, Udita
van Staaden, Moira
Huber, Robert
author_facet Datta, Udita
van Staaden, Moira
Huber, Robert
author_sort Datta, Udita
collection PubMed
description Natural reward is an essential element of any organism’s ability to adapt to environmental variation. Its underlying circuits and mechanisms guide the learning process as they help associate an event, or cue, with the perception of an outcome’s value. More generally, natural reward serves as the fundamental generator of all motivated behavior. Addictive plant alkaloids are able to activate this circuitry in taxa ranging from planaria to humans. With modularly organized nervous systems and confirmed vulnerabilities to human drugs of abuse, crayfish have recently emerged as a compelling model for the study of the addiction cycle, including psychostimulant effects, sensitization, withdrawal, reinstatement, and drug reward in conditioned place preference paradigms. Here we extend this work with the demonstration of a spatially contingent, operant drug self-administration paradigm for amphetamine. When the animal enters a quadrant of the arena with a particular textured substrate, a computer-based control system delivers amphetamine through an indwelling fine-bore cannula. Resulting reward strength, dose-response, and the time course of operant conditioning were assessed. Individuals experiencing the drug contingent on their behavior, displayed enhanced rates of operant responses compared to that of their yoked (non-contingent) counterparts. Application of amphetamine near the supra-esophageal ganglion elicited stronger and more robust increases in operant responding than did systemic infusions. This work demonstrates automated implementation of a spatially contingent self-administration paradigm in crayfish, which provides a powerful tool to explore comparative perspectives in drug-sensitive reward, the mechanisms of learning underlying the addictive cycle, and phylogenetically conserved vulnerabilities to psychostimulant compounds.
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spelling pubmed-59615112018-06-04 Crayfish Self-Administer Amphetamine in a Spatially Contingent Task Datta, Udita van Staaden, Moira Huber, Robert Front Physiol Physiology Natural reward is an essential element of any organism’s ability to adapt to environmental variation. Its underlying circuits and mechanisms guide the learning process as they help associate an event, or cue, with the perception of an outcome’s value. More generally, natural reward serves as the fundamental generator of all motivated behavior. Addictive plant alkaloids are able to activate this circuitry in taxa ranging from planaria to humans. With modularly organized nervous systems and confirmed vulnerabilities to human drugs of abuse, crayfish have recently emerged as a compelling model for the study of the addiction cycle, including psychostimulant effects, sensitization, withdrawal, reinstatement, and drug reward in conditioned place preference paradigms. Here we extend this work with the demonstration of a spatially contingent, operant drug self-administration paradigm for amphetamine. When the animal enters a quadrant of the arena with a particular textured substrate, a computer-based control system delivers amphetamine through an indwelling fine-bore cannula. Resulting reward strength, dose-response, and the time course of operant conditioning were assessed. Individuals experiencing the drug contingent on their behavior, displayed enhanced rates of operant responses compared to that of their yoked (non-contingent) counterparts. Application of amphetamine near the supra-esophageal ganglion elicited stronger and more robust increases in operant responding than did systemic infusions. This work demonstrates automated implementation of a spatially contingent self-administration paradigm in crayfish, which provides a powerful tool to explore comparative perspectives in drug-sensitive reward, the mechanisms of learning underlying the addictive cycle, and phylogenetically conserved vulnerabilities to psychostimulant compounds. Frontiers Media S.A. 2018-05-14 /pmc/articles/PMC5961511/ /pubmed/29867520 http://dx.doi.org/10.3389/fphys.2018.00433 Text en Copyright © 2018 Datta, van Staaden and Huber. 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 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 Physiology
Datta, Udita
van Staaden, Moira
Huber, Robert
Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title_full Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title_fullStr Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title_full_unstemmed Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title_short Crayfish Self-Administer Amphetamine in a Spatially Contingent Task
title_sort crayfish self-administer amphetamine in a spatially contingent task
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961511/
https://www.ncbi.nlm.nih.gov/pubmed/29867520
http://dx.doi.org/10.3389/fphys.2018.00433
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