Cargando…

Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice

BACKGROUND: Isolation-reared mice show social encounter-induced hyperactivity with activation of prefrontal serotonergic and dopaminergic systems, but it is not known whether this stress response is observed in other pathological conditions. Here we examined whether the social encounter stimulation...

Descripción completa

Detalles Bibliográficos
Autores principales: Tanaka, Tatsunori, Ago, Yukio, Umehara, Chiaki, Imoto, Emina, Hasebe, Shigeru, Hashimoto, Hitoshi, Takuma, Kazuhiro, Matsuda, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417057/
https://www.ncbi.nlm.nih.gov/pubmed/28034961
http://dx.doi.org/10.1093/ijnp/pyw115
_version_ 1783233858604367872
author Tanaka, Tatsunori
Ago, Yukio
Umehara, Chiaki
Imoto, Emina
Hasebe, Shigeru
Hashimoto, Hitoshi
Takuma, Kazuhiro
Matsuda, Toshio
author_facet Tanaka, Tatsunori
Ago, Yukio
Umehara, Chiaki
Imoto, Emina
Hasebe, Shigeru
Hashimoto, Hitoshi
Takuma, Kazuhiro
Matsuda, Toshio
author_sort Tanaka, Tatsunori
collection PubMed
description BACKGROUND: Isolation-reared mice show social encounter-induced hyperactivity with activation of prefrontal serotonergic and dopaminergic systems, but it is not known whether this stress response is observed in other pathological conditions. Here we examined whether the social encounter stimulation induces abnormal behavior during withdrawal in chronic methamphetamine-treated mice. METHODS: To induce methamphetamine-induced behavioral sensitization, male mice were injected with methamphetamine (1 mg/kg) once daily for 7 days. RESULTS: The encounter with an intruder elicited hyperactivity 24 h after the last injection of methamphetamine in methamphetamine-sensitized mice. This response was observed even as long as 2 weeks after withdrawal of methamphetamine. The encounter increased c-Fos expression in the prefrontal cortex, dorsal raphe nucleus and ventral tegmental area in methamphetamine-sensitized mice, while it did not in control mice. Furthermore, the encounter increased extracellular serotonin (5-HT) and dopamine, but not noradrenaline, levels in the prefrontal cortex in methamphetamine-sensitized mice. Local injection of 5,7-dihydroxytryptamine and 6-hydroxydopamine into the prefrontal cortex attenuated encounter-induced hyperactivity in methamphetamine-sensitized mice and it markedly decreased prefrontal 5-HT and dopamine levels, respectively. Pharmacological analysis showed that the encounter-induced hyperactivity is mediated by dopamine D(1) receptors and 5-HT(2A) receptors and attenuated by anxiolytics and antidepressants such as diazepam, osemozotan and selective 5-HT reuptake inhibitors. The effect of paroxetine was blocked by the 5-HT(3) receptor antagonist azasetron. CONCLUSIONS: The present study shows that psychological stress elicits hyperactivity with activation of prefrontal 5-HT and dopamine systems in methamphetamine-dependent mice and suggests that the abnormal behavior is associated with anxiety and depression.
format Online
Article
Text
id pubmed-5417057
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-54170572017-05-05 Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice Tanaka, Tatsunori Ago, Yukio Umehara, Chiaki Imoto, Emina Hasebe, Shigeru Hashimoto, Hitoshi Takuma, Kazuhiro Matsuda, Toshio Int J Neuropsychopharmacol Regular Research Article BACKGROUND: Isolation-reared mice show social encounter-induced hyperactivity with activation of prefrontal serotonergic and dopaminergic systems, but it is not known whether this stress response is observed in other pathological conditions. Here we examined whether the social encounter stimulation induces abnormal behavior during withdrawal in chronic methamphetamine-treated mice. METHODS: To induce methamphetamine-induced behavioral sensitization, male mice were injected with methamphetamine (1 mg/kg) once daily for 7 days. RESULTS: The encounter with an intruder elicited hyperactivity 24 h after the last injection of methamphetamine in methamphetamine-sensitized mice. This response was observed even as long as 2 weeks after withdrawal of methamphetamine. The encounter increased c-Fos expression in the prefrontal cortex, dorsal raphe nucleus and ventral tegmental area in methamphetamine-sensitized mice, while it did not in control mice. Furthermore, the encounter increased extracellular serotonin (5-HT) and dopamine, but not noradrenaline, levels in the prefrontal cortex in methamphetamine-sensitized mice. Local injection of 5,7-dihydroxytryptamine and 6-hydroxydopamine into the prefrontal cortex attenuated encounter-induced hyperactivity in methamphetamine-sensitized mice and it markedly decreased prefrontal 5-HT and dopamine levels, respectively. Pharmacological analysis showed that the encounter-induced hyperactivity is mediated by dopamine D(1) receptors and 5-HT(2A) receptors and attenuated by anxiolytics and antidepressants such as diazepam, osemozotan and selective 5-HT reuptake inhibitors. The effect of paroxetine was blocked by the 5-HT(3) receptor antagonist azasetron. CONCLUSIONS: The present study shows that psychological stress elicits hyperactivity with activation of prefrontal 5-HT and dopamine systems in methamphetamine-dependent mice and suggests that the abnormal behavior is associated with anxiety and depression. Oxford University Press 2016-12-29 /pmc/articles/PMC5417057/ /pubmed/28034961 http://dx.doi.org/10.1093/ijnp/pyw115 Text en © The Author 2016. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Research Article
Tanaka, Tatsunori
Ago, Yukio
Umehara, Chiaki
Imoto, Emina
Hasebe, Shigeru
Hashimoto, Hitoshi
Takuma, Kazuhiro
Matsuda, Toshio
Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title_full Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title_fullStr Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title_full_unstemmed Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title_short Role of Prefrontal Serotonergic and Dopaminergic Systems in Encounter-Induced Hyperactivity in Methamphetamine-Sensitized Mice
title_sort role of prefrontal serotonergic and dopaminergic systems in encounter-induced hyperactivity in methamphetamine-sensitized mice
topic Regular Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417057/
https://www.ncbi.nlm.nih.gov/pubmed/28034961
http://dx.doi.org/10.1093/ijnp/pyw115
work_keys_str_mv AT tanakatatsunori roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT agoyukio roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT umeharachiaki roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT imotoemina roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT hasebeshigeru roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT hashimotohitoshi roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT takumakazuhiro roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice
AT matsudatoshio roleofprefrontalserotonergicanddopaminergicsystemsinencounterinducedhyperactivityinmethamphetaminesensitizedmice