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Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats

High doses of the nicotinic acetylcholine receptor (nAChR) antagonist mecamylamine can elicit somatic signs resembling those associated with nicotine withdrawal in nicotine-naïve adult rats. Understanding this phenomenon, and its possible modulation by acute nicotine and age, could inform the use of...

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Autores principales: Schmidt, Clare E., Manbeck, Katherine E., Shelley, David, Harris, Andrew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611158/
https://www.ncbi.nlm.nih.gov/pubmed/26539119
http://dx.doi.org/10.3389/fphar.2015.00239
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author Schmidt, Clare E.
Manbeck, Katherine E.
Shelley, David
Harris, Andrew C.
author_facet Schmidt, Clare E.
Manbeck, Katherine E.
Shelley, David
Harris, Andrew C.
author_sort Schmidt, Clare E.
collection PubMed
description High doses of the nicotinic acetylcholine receptor (nAChR) antagonist mecamylamine can elicit somatic signs resembling those associated with nicotine withdrawal in nicotine-naïve adult rats. Understanding this phenomenon, and its possible modulation by acute nicotine and age, could inform the use of mecamylamine as both an experimental tool and potential pharmacotherapy for tobacco dependence and other disorders. This study evaluated the ability of high-dose mecamylamine to elicit somatic signs in adolescent rats, and the potential for acute nicotine pretreatment to potentiate this effect as previously reported in adults. Single or repeated injections of mecamylamine (1.5 or 3.0 mg/kg, s.c.) elicited somatic signs in nicotine-naïve adolescents, but this effect was not influenced by 2 h pretreatment with acute nicotine (0.5 mg/kg, s.c.). In an initial evaluation of the effects of age in this model, mecamylamine (2.25 mg/kg, s.c.) elicited somatic signs in nicotine-naïve adolescents and adults. This effect was modestly enhanced following acute nicotine injections in adults but not in adolescents, even when a higher nicotine dose (1.0 rather than 0.5 mg/kg, s.c.) was used in adolescents to account for age differences in nicotine pharmacokinetics. These studies are the first to show that mecamylamine elicits somatic signs in nicotine-naïve adolescent rats, an effect that should be considered when designing and interpreting studies examining effects of high doses of mecamylamine in adolescents. Our findings also provide preliminary evidence that these signs may be differentially modulated by acute nicotine pretreatment in adolescents versus adults.
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spelling pubmed-46111582015-11-04 Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats Schmidt, Clare E. Manbeck, Katherine E. Shelley, David Harris, Andrew C. Front Pharmacol Pharmacology High doses of the nicotinic acetylcholine receptor (nAChR) antagonist mecamylamine can elicit somatic signs resembling those associated with nicotine withdrawal in nicotine-naïve adult rats. Understanding this phenomenon, and its possible modulation by acute nicotine and age, could inform the use of mecamylamine as both an experimental tool and potential pharmacotherapy for tobacco dependence and other disorders. This study evaluated the ability of high-dose mecamylamine to elicit somatic signs in adolescent rats, and the potential for acute nicotine pretreatment to potentiate this effect as previously reported in adults. Single or repeated injections of mecamylamine (1.5 or 3.0 mg/kg, s.c.) elicited somatic signs in nicotine-naïve adolescents, but this effect was not influenced by 2 h pretreatment with acute nicotine (0.5 mg/kg, s.c.). In an initial evaluation of the effects of age in this model, mecamylamine (2.25 mg/kg, s.c.) elicited somatic signs in nicotine-naïve adolescents and adults. This effect was modestly enhanced following acute nicotine injections in adults but not in adolescents, even when a higher nicotine dose (1.0 rather than 0.5 mg/kg, s.c.) was used in adolescents to account for age differences in nicotine pharmacokinetics. These studies are the first to show that mecamylamine elicits somatic signs in nicotine-naïve adolescent rats, an effect that should be considered when designing and interpreting studies examining effects of high doses of mecamylamine in adolescents. Our findings also provide preliminary evidence that these signs may be differentially modulated by acute nicotine pretreatment in adolescents versus adults. Frontiers Media S.A. 2015-10-20 /pmc/articles/PMC4611158/ /pubmed/26539119 http://dx.doi.org/10.3389/fphar.2015.00239 Text en Copyright © 2015 Schmidt, Manbeck, Shelley and Harris. 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) or licensor 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 Pharmacology
Schmidt, Clare E.
Manbeck, Katherine E.
Shelley, David
Harris, Andrew C.
Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title_full Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title_fullStr Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title_full_unstemmed Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title_short Blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
title_sort blockade of cholinergic transmission elicits somatic signs in nicotine-naïve adolescent rats
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611158/
https://www.ncbi.nlm.nih.gov/pubmed/26539119
http://dx.doi.org/10.3389/fphar.2015.00239
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