Evidence map›Paper›PMID 41051707›Full record

ReviewAdvances in neurobiology2025

Regulation of Dopamine Transporter Surface Expression.

Christina Besada, Ole Valente Mortensen

Abstract readReview
In one paragraph

Review in Advances in neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Christina BesadaDepartment of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA, USA.
Ole Valente MortensenDepartment of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA, USA. ovm23@drexel.edu.

Funding

Computational and functional studies of allosteric monoamine transporter modulationR01MH106912 · NIMH · DREXEL UNIVERSITY · PI KORTAGERE, SANDHYA, MORTENSEN, OLE VALENTE · 2015 to 2019
$2.0M
Allosteric modulation of dopamine transport-Functional and Biochemical StudiesR56MH121453 · NIMH · DREXEL UNIVERSITY · PI MORTENSEN, OLE VALENTE · 2020 to 2021
$783k
Selective real-time activation of ERK1/2 signaling in dopamine neuronsR21DA057054 · NIDA · DREXEL UNIVERSITY · PI ESPAÑA, RODRIGO A., MORTENSEN, OLE VALENTE · 2022 to 2023
$417k
NIDA NIH HHS R21 DA057054NIMH NIH HHS R01 MH106912NIMH NIH HHS R56 MH121453
6 · The paper itself

Abstract

The dopamine transporter (DAT) is a plasma membrane protein expressed in dopamine (DA) neurons of the central nervous system and is critical for regulating DA neurotransmission. The DAT is responsible for the reuptake of released DA back into the presynaptic neuron, resulting in the termination of DA transmission. This process also recycles the DA back into the dopaminergic neuron for subsequent release. DAT is the target of psychostimulants including cocaine and amphetamines and has been associated with several neuropsychiatric disorders. Only DAT proteins located on the plasma membrane can remove DA from the extracellular space, and the number of DAT proteins on the cell-surface therefore determines the efficiency of DA clearance. As a result, regulating DAT surface expression is a critical means to regulating the magnitude and duration of DA neurotransmission. This chapter will discuss the different processes and proteins that have been shown to affect DAT surface expression and discuss the relevance to normal DA physiology and diseases that involve aberrant DA signaling.

Indexed as

Cell MembraneDopamineDopamine Plasma Membrane Transport ProteinsDopaminergic NeuronsAnimalsHumansSynaptic TransmissionDopamineDopamine Plasma Membrane Transport ProteinsAmphetamineCocaineDopamine transporterEndocytosisMembrane protein traffickingPsychostimulants

Identifiers

PMID41051707
PMCPMC12598116

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.