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Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum

Cigarette smoke is a highly complex mixture of nicotine and non-nicotine constituents. Exposure to cigarette smoke enhances tobacco dependence by potentiating glutamatergic neurotransmission via stimulation of nicotinic acetylcholine receptors (nAChRs). We investigated the effects of nicotine and no...

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Autores principales: Ryu, In Soo, Kim, Jieun, Yang, Ju Hwan, Seo, Su Yeon, Sohn, Sumin, Kim, Sunghyun, Lee, Kyuhong, Seo, Joung-Wook, Choe, Eun Sang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830476/
https://www.ncbi.nlm.nih.gov/pubmed/33374316
http://dx.doi.org/10.3390/brainsci11010014
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author Ryu, In Soo
Kim, Jieun
Yang, Ju Hwan
Seo, Su Yeon
Sohn, Sumin
Kim, Sunghyun
Lee, Kyuhong
Seo, Joung-Wook
Choe, Eun Sang
author_facet Ryu, In Soo
Kim, Jieun
Yang, Ju Hwan
Seo, Su Yeon
Sohn, Sumin
Kim, Sunghyun
Lee, Kyuhong
Seo, Joung-Wook
Choe, Eun Sang
author_sort Ryu, In Soo
collection PubMed
description Cigarette smoke is a highly complex mixture of nicotine and non-nicotine constituents. Exposure to cigarette smoke enhances tobacco dependence by potentiating glutamatergic neurotransmission via stimulation of nicotinic acetylcholine receptors (nAChRs). We investigated the effects of nicotine and non-nicotine alkaloids in the cigarette smoke condensates extracted from two commercial cigarette brands in South Korea (KCSC A and KCSC B) on psychomotor behaviors and glutamate levels in the dorsal striatum. Repeated and challenge administration of KCSCs (nicotine content: 0.4 mg/kg, subcutaneous) increased psychomotor behaviors (ambulatory, rearing, and rotational activities) and time spent in psychoactive behavioral states compared to exposure to nicotine (0.4 mg/kg) alone. The increase in psychomotor behaviors lasted longer when exposed to repeated and challenge administration of KCSCs compared to nicotine alone. In parallel with sustained increase in psychomotor behaviors, repeated administration of KCSCs also caused long-lasting glutamate release in the dorsal striatum compared to nicotine alone. KCSC-induced changes in psychomotor behaviors and glutamate levels in the dorsal striatum were found to be strongly correlated. These findings suggest that non-nicotine alkaloids in commercial cigarette smoke synergistically act with nicotine on nAChRs, thereby upregulating glutamatergic response in the dorsal striatum, which contributes to the hypersensitization of psychomotor behaviors.
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spelling pubmed-78304762021-01-26 Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum Ryu, In Soo Kim, Jieun Yang, Ju Hwan Seo, Su Yeon Sohn, Sumin Kim, Sunghyun Lee, Kyuhong Seo, Joung-Wook Choe, Eun Sang Brain Sci Article Cigarette smoke is a highly complex mixture of nicotine and non-nicotine constituents. Exposure to cigarette smoke enhances tobacco dependence by potentiating glutamatergic neurotransmission via stimulation of nicotinic acetylcholine receptors (nAChRs). We investigated the effects of nicotine and non-nicotine alkaloids in the cigarette smoke condensates extracted from two commercial cigarette brands in South Korea (KCSC A and KCSC B) on psychomotor behaviors and glutamate levels in the dorsal striatum. Repeated and challenge administration of KCSCs (nicotine content: 0.4 mg/kg, subcutaneous) increased psychomotor behaviors (ambulatory, rearing, and rotational activities) and time spent in psychoactive behavioral states compared to exposure to nicotine (0.4 mg/kg) alone. The increase in psychomotor behaviors lasted longer when exposed to repeated and challenge administration of KCSCs compared to nicotine alone. In parallel with sustained increase in psychomotor behaviors, repeated administration of KCSCs also caused long-lasting glutamate release in the dorsal striatum compared to nicotine alone. KCSC-induced changes in psychomotor behaviors and glutamate levels in the dorsal striatum were found to be strongly correlated. These findings suggest that non-nicotine alkaloids in commercial cigarette smoke synergistically act with nicotine on nAChRs, thereby upregulating glutamatergic response in the dorsal striatum, which contributes to the hypersensitization of psychomotor behaviors. MDPI 2020-12-24 /pmc/articles/PMC7830476/ /pubmed/33374316 http://dx.doi.org/10.3390/brainsci11010014 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ryu, In Soo
Kim, Jieun
Yang, Ju Hwan
Seo, Su Yeon
Sohn, Sumin
Kim, Sunghyun
Lee, Kyuhong
Seo, Joung-Wook
Choe, Eun Sang
Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title_full Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title_fullStr Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title_full_unstemmed Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title_short Exposure to Commercial Cigarette Smoke Produces Psychomotor Sensitization via Hyperstimulation of Glutamate Response in the Dorsal Striatum
title_sort exposure to commercial cigarette smoke produces psychomotor sensitization via hyperstimulation of glutamate response in the dorsal striatum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830476/
https://www.ncbi.nlm.nih.gov/pubmed/33374316
http://dx.doi.org/10.3390/brainsci11010014
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