Noradrenergic terminals are the primary source of α
Adrenergic Neurons
/ drug effects
Adrenergic alpha-2 Receptor Agonists
/ pharmacology
Adrenergic alpha-2 Receptor Antagonists
/ pharmacology
Animals
Dopamine
/ metabolism
Fluoxetine
/ analogs & derivatives
Imidazoles
/ pharmacology
Male
Norepinephrine
/ metabolism
Norepinephrine Plasma Membrane Transport Proteins
/ antagonists & inhibitors
Prefrontal Cortex
/ drug effects
Rats, Sprague-Dawley
Receptors, Adrenergic, alpha-2
/ metabolism
Anti-DBH-saporin
Co-release
D(2)-antagonist
Microdialysis
Norepinephrine transporter
Journal
Progress in neuro-psychopharmacology & biological psychiatry
ISSN: 1878-4216
Titre abrégé: Prog Neuropsychopharmacol Biol Psychiatry
Pays: England
ID NLM: 8211617
Informations de publication
Date de publication:
02 03 2019
02 03 2019
Historique:
received:
23
07
2018
revised:
20
11
2018
accepted:
21
11
2018
pubmed:
26
11
2018
medline:
23
4
2019
entrez:
26
11
2018
Statut:
ppublish
Résumé
In various psychiatric disorders, deficits in dopaminergic activity in the prefrontal cortex (PFC) are implicated. Treatments involving selective augmentation of dopaminergic activity in the PFC primarily depend on the inhibition of α
Identifiants
pubmed: 30472147
pii: S0278-5846(18)30564-5
doi: 10.1016/j.pnpbp.2018.11.015
pii:
doi:
Substances chimiques
Adrenergic alpha-2 Receptor Agonists
0
Adrenergic alpha-2 Receptor Antagonists
0
Imidazoles
0
Norepinephrine Plasma Membrane Transport Proteins
0
Receptors, Adrenergic, alpha-2
0
Fluoxetine
01K63SUP8D
atipamezole
03N9U5JAF6
nisoxetine
17NV064B2D
Dopamine
VTD58H1Z2X
Norepinephrine
X4W3ENH1CV
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
97-103Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.