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Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice

RATIONALE: Testing genetically engineered mice in a reliable nicotine self-administration procedure could provide important insights into the molecular mechanisms underlying nicotine reinforcement. OBJECTIVES: We assessed operant responding for intravenous nicotine infusions in C57BL/6J male mice un...

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Detalles Bibliográficos
Autores principales: Contet, Candice, Whisler, Kimberly N., Jarrell, Holly, Kenny, Paul J., Markou, Athina
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952765/
https://www.ncbi.nlm.nih.gov/pubmed/20668842
http://dx.doi.org/10.1007/s00213-010-1950-4
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author Contet, Candice
Whisler, Kimberly N.
Jarrell, Holly
Kenny, Paul J.
Markou, Athina
author_facet Contet, Candice
Whisler, Kimberly N.
Jarrell, Holly
Kenny, Paul J.
Markou, Athina
author_sort Contet, Candice
collection PubMed
description RATIONALE: Testing genetically engineered mice in a reliable nicotine self-administration procedure could provide important insights into the molecular mechanisms underlying nicotine reinforcement. OBJECTIVES: We assessed operant responding for intravenous nicotine infusions in C57BL/6J male mice under a fixed-ratio 3 schedule of reinforcement in which a visual cue was contingently associated with drug delivery. METHODS/RESULTS: Acquisition, dose-response function, extinction, and cue-induced reinstatement of operant behavior were characterized. Low nicotine doses (0.001-0.06 mg/kg/infusion) elicited response rates similar to those supported by saline, whereas a higher dose (0.1 mg/kg/infusion) decreased responding. Using an identical procedure to assess cocaine self-administration in an independent group of mice yielded an inverted U-shaped dose-response curve. Other mice trained to respond exclusively for the visual stimulus earned a similar number of reinforcers as mice self-administering saline or low nicotine doses, although with a lower selectivity for the active lever and their response rates were sensitive to the discontinuation and resumption of cue light presentation. Finally, patterns of responding for nicotine, cocaine, or the visual stimulus alone were analyzed using frequency distributions of inter-response intervals and extended return maps. These analyses revealed unique properties of nicotine, which dose-dependently delayed the first response post-timeout and increased the regularity of lever pressing activity. CONCLUSIONS: Nicotine did not enhance the reinforcing properties of the visual cue paired with drug delivery. Interestingly, however, patterns of responding could differentiate nicotine self-administration from responding for a visual stimulus or saline and indicated that nicotine functioned as a salient stimulus driving highly regular operant behavior. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00213-010-1950-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-29527652010-10-21 Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice Contet, Candice Whisler, Kimberly N. Jarrell, Holly Kenny, Paul J. Markou, Athina Psychopharmacology (Berl) Original Investigation RATIONALE: Testing genetically engineered mice in a reliable nicotine self-administration procedure could provide important insights into the molecular mechanisms underlying nicotine reinforcement. OBJECTIVES: We assessed operant responding for intravenous nicotine infusions in C57BL/6J male mice under a fixed-ratio 3 schedule of reinforcement in which a visual cue was contingently associated with drug delivery. METHODS/RESULTS: Acquisition, dose-response function, extinction, and cue-induced reinstatement of operant behavior were characterized. Low nicotine doses (0.001-0.06 mg/kg/infusion) elicited response rates similar to those supported by saline, whereas a higher dose (0.1 mg/kg/infusion) decreased responding. Using an identical procedure to assess cocaine self-administration in an independent group of mice yielded an inverted U-shaped dose-response curve. Other mice trained to respond exclusively for the visual stimulus earned a similar number of reinforcers as mice self-administering saline or low nicotine doses, although with a lower selectivity for the active lever and their response rates were sensitive to the discontinuation and resumption of cue light presentation. Finally, patterns of responding for nicotine, cocaine, or the visual stimulus alone were analyzed using frequency distributions of inter-response intervals and extended return maps. These analyses revealed unique properties of nicotine, which dose-dependently delayed the first response post-timeout and increased the regularity of lever pressing activity. CONCLUSIONS: Nicotine did not enhance the reinforcing properties of the visual cue paired with drug delivery. Interestingly, however, patterns of responding could differentiate nicotine self-administration from responding for a visual stimulus or saline and indicated that nicotine functioned as a salient stimulus driving highly regular operant behavior. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00213-010-1950-4) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-07-29 2010 /pmc/articles/PMC2952765/ /pubmed/20668842 http://dx.doi.org/10.1007/s00213-010-1950-4 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Investigation
Contet, Candice
Whisler, Kimberly N.
Jarrell, Holly
Kenny, Paul J.
Markou, Athina
Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title_full Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title_fullStr Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title_full_unstemmed Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title_short Patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in C57BL/6J mice
title_sort patterns of responding differentiate intravenous nicotine self-administration from responding for a visual stimulus in c57bl/6j mice
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952765/
https://www.ncbi.nlm.nih.gov/pubmed/20668842
http://dx.doi.org/10.1007/s00213-010-1950-4
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