Organic cation transporter 3 and the dopamine transporter differentially regulate catecholamine uptake in the basolateral amygdala and nucleus accumbens.


Journal

The European journal of neuroscience
ISSN: 1460-9568
Titre abrégé: Eur J Neurosci
Pays: France
ID NLM: 8918110

Informations de publication

Date de publication:
12 2020
Historique:
received: 29 08 2019
revised: 28 03 2020
accepted: 24 04 2020
pubmed: 30 7 2020
medline: 22 6 2021
entrez: 30 7 2020
Statut: ppublish

Résumé

Regional alterations in kinetics of catecholamine uptake are due in part to variations in clearance mechanisms. The rate of clearance is a critical determinant of the strength of catecholamine signaling. Catecholamine transmission in the nucleus accumbens core (NAcc) and basolateral amygdala (BLA) is of particular interest due to involvement of these regions in cognition and motivation. Previous work has shown that catecholamine clearance in the NAcc is largely mediated by the dopamine transporter (DAT), but clearance in the BLA is less DAT-dependent. A growing body of literature suggests that organic cation transporter 3 (OCT3) also contributes to catecholamine clearance in both regions. Consistent with different clearance mechanisms between regions, catecholamine clearance is more rapid in the NAcc than in the BLA, though mechanisms underlying this have not been resolved. We compared the expression of DAT and OCT3 and their contributions to catecholamine clearance in the NAcc and BLA. We found DAT protein levels were ~ 4-fold higher in the NAcc than in the BLA, while OCT3 protein expression was similar between the two regions. Immunofluorescent labeling of the two transporters in brain sections confirmed these findings. Ex vivo voltammetry demonstrated that the magnitude of catecholamine release was greater, and the clearance rate was faster in the NAcc than in the BLA. Additionally, catecholamine clearance in the BLA was more sensitive to the OCT3 inhibitor corticosterone, while clearance in the NAcc was more cocaine sensitive. These distinctions in catecholamine clearance may underlie differential effects of catecholamines on behavioral outputs mediated by these regions.

Identifiants

pubmed: 32725894
doi: 10.1111/ejn.14927
pmc: PMC7775350
mid: NIHMS1628053
doi:

Substances chimiques

Catecholamines 0
Cations 0
Dopamine Plasma Membrane Transport Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4546-4562

Subventions

Organisme : NIAAA NIH HHS
ID : P50 AA026117
Pays : United States
Organisme : NIAAA NIH HHS
ID : P50 AA12298125
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA023999
Pays : United States
Organisme : NIAAA NIH HHS
ID : T32 AA007565
Pays : United States
Organisme : NIAAA NIH HHS
ID : P01 AA021099
Pays : United States
Organisme : NIDA NIH HHS
ID : F31 DA035558
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA014030
Pays : United States
Organisme : SRJ
ID : P50 DA0066
Organisme : NIDA NIH HHS
ID : R01 DA048490
Pays : United States
Organisme : NIAAA NIH HHS
ID : U01 AA014091
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032895
Pays : United States
Organisme : NIDA NIH HHS
ID : P50 DA006634
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA041349
Pays : United States

Informations de copyright

© 2020 Federation of European Neuroscience Societies and John Wiley & Sons Ltd.

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Auteurs

Katherine M Holleran (KM)

Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Jamie H Rose (JH)

Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Steven C Fordahl (SC)

Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

Kelsey C Benton (KC)

Department of Biomedical Sciences, Marquette University, Milwaukee, WI, USA.

Kayla E Rohr (KE)

Department of Biomedical Sciences, Marquette University, Milwaukee, WI, USA.

Paul J Gasser (PJ)

Department of Biomedical Sciences, Marquette University, Milwaukee, WI, USA.

Sara R Jones (SR)

Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

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