Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats

Abstract Aim Our previous studies showed that exposure to acute restraint stress enhanced cocaine‐induced conditioned place preference (cocaine‐CPP) and suggested the possibility that co‐activation of adrenergic transmission boosts the increase in medial prefrontal cortex (mPFC) neuronal activity by...

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Main Authors: Fumiya Shinohara, Saya Arakaki, Taiju Amano, Masabumi Minami, Katsuyuki Kaneda
Format: Article
Language:English
Published: Wiley 2020-12-01
Series:Neuropsychopharmacology Reports
Subjects:
Online Access:https://doi.org/10.1002/npr2.12135
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author Fumiya Shinohara
Saya Arakaki
Taiju Amano
Masabumi Minami
Katsuyuki Kaneda
author_facet Fumiya Shinohara
Saya Arakaki
Taiju Amano
Masabumi Minami
Katsuyuki Kaneda
author_sort Fumiya Shinohara
collection DOAJ
description Abstract Aim Our previous studies showed that exposure to acute restraint stress enhanced cocaine‐induced conditioned place preference (cocaine‐CPP) and suggested the possibility that co‐activation of adrenergic transmission boosts the increase in medial prefrontal cortex (mPFC) neuronal activity by the activation of dopaminergic transmission. To examine this possibility, the effects of the co‐treatment with dopamine (DA) and noradrenaline (NA) on mPFC neurons were compared with those of treatment with DA alone using whole‐cell patch‐clamp recordings. Methods The effects of DA alone and a mixture of DA and NA on the membrane potentials and spontaneous excitatory postsynaptic currents (sEPSCs) were examined by electrophysiological recordings of mPFC pyramidal neurons in brain slices of male Sprague Dawley rats. Extracellular DA and NA levels in the mPFC during and after restraint stress exposure were also examined by in vivo microdialysis. Results Dopamine significantly produced depolarizing effects on mPFC neurons and tended to increase sEPSC frequency. Co‐administration of NA with DA produced stronger depolarizing effects and significantly increased sEPSC frequency. The findings suggest that the additional depolarizing effect of NA on DA‐responsive neurons, rather than the excitation of DA‐nonresponsive neurons by NA, contributes to the stronger effect of co‐treatment of NA with DA. Conclusion The present study suggests that NA released by restraint stress exposure cooperates with DA to stimulate DA‐responsive neurons in the mPFC, thereby causing the stress‐induced enhancement of cocaine‐CPP.
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spelling doaj.art-bbf2b967563d4395ad9bc078a19762752022-12-22T04:21:44ZengWileyNeuropsychopharmacology Reports2574-173X2020-12-0140434835410.1002/npr2.12135Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in ratsFumiya Shinohara0Saya Arakaki1Taiju Amano2Masabumi Minami3Katsuyuki Kaneda4Department of Pharmacology Graduate School of Pharmaceutical Sciences Hokkaido University Sapporo JapanDepartment of Pharmacology Graduate School of Pharmaceutical Sciences Hokkaido University Sapporo JapanDepartment of Pharmacology Graduate School of Pharmaceutical Sciences Hokkaido University Sapporo JapanDepartment of Pharmacology Graduate School of Pharmaceutical Sciences Hokkaido University Sapporo JapanLaboratory of Molecular Pharmacology Institute of Medical, Pharmaceutical and Health Sciences Kanazawa University Kanazawa JapanAbstract Aim Our previous studies showed that exposure to acute restraint stress enhanced cocaine‐induced conditioned place preference (cocaine‐CPP) and suggested the possibility that co‐activation of adrenergic transmission boosts the increase in medial prefrontal cortex (mPFC) neuronal activity by the activation of dopaminergic transmission. To examine this possibility, the effects of the co‐treatment with dopamine (DA) and noradrenaline (NA) on mPFC neurons were compared with those of treatment with DA alone using whole‐cell patch‐clamp recordings. Methods The effects of DA alone and a mixture of DA and NA on the membrane potentials and spontaneous excitatory postsynaptic currents (sEPSCs) were examined by electrophysiological recordings of mPFC pyramidal neurons in brain slices of male Sprague Dawley rats. Extracellular DA and NA levels in the mPFC during and after restraint stress exposure were also examined by in vivo microdialysis. Results Dopamine significantly produced depolarizing effects on mPFC neurons and tended to increase sEPSC frequency. Co‐administration of NA with DA produced stronger depolarizing effects and significantly increased sEPSC frequency. The findings suggest that the additional depolarizing effect of NA on DA‐responsive neurons, rather than the excitation of DA‐nonresponsive neurons by NA, contributes to the stronger effect of co‐treatment of NA with DA. Conclusion The present study suggests that NA released by restraint stress exposure cooperates with DA to stimulate DA‐responsive neurons in the mPFC, thereby causing the stress‐induced enhancement of cocaine‐CPP.https://doi.org/10.1002/npr2.12135cocainedopaminemedial prefrontal cortexnoradrenalinestress
spellingShingle Fumiya Shinohara
Saya Arakaki
Taiju Amano
Masabumi Minami
Katsuyuki Kaneda
Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
Neuropsychopharmacology Reports
cocaine
dopamine
medial prefrontal cortex
noradrenaline
stress
title Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
title_full Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
title_fullStr Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
title_full_unstemmed Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
title_short Noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
title_sort noradrenaline enhances the excitatory effects of dopamine on medial prefrontal cortex pyramidal neurons in rats
topic cocaine
dopamine
medial prefrontal cortex
noradrenaline
stress
url https://doi.org/10.1002/npr2.12135
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