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Monoamine transporter (with three canonical members: Dopamine transporter, Norepinephrine transporter, Serotonin transporter) (MAT (also DAT, NET, SERT for specific subtypes))

Target
MAT (also DAT, NET, SERT for specific subtypes)
Molecular classification
Transporter, Solute carrier family (SLC6), Neurotransmitter:sodium symporter (NSS) family
01

Overview

Monoamine transporters are membrane proteins responsible for the reuptake of monoamine neurotransmitters—dopamine, norepinephrine, and serotonin—from the synaptic cleft into presynaptic neurons, thereby regulating neurotransmitter levels and controlling synaptic signaling duration and strength. These transporters are key pharmacological targets for antidepressants, psychostimulants, and drugs used in treating neuropsychiatric and neurodegenerative disorders. The term “monoamine reuptake” specifically refers to the function by which these proteins operate. Drugs that inhibit monoamine reuptake increase extracellular monoamine concentrations, leading to enhanced neurotransmission and various therapeutic or psychoactive effects.

Other names
Monoamine transporterMonoamine reuptake transporterMATSLC6 family transporterNa⁺/Cl⁻-dependent neurotransmitter transporter
02

Mechanism of action

Inhibition of transporter-mediated reuptake, leading to increased extracellular monoamine concentration; Competitive or non-competitive binding at the transporter site; Substrate reversal (e.g. amphetamines can cause net release via “reverse transport”)

03

Biological functions

Neurotransmitter reuptake (dopamine, serotonin, norepinephrine)Regulation of synaptic neurotransmitter levelsTermination of neurotransmitter signaling
04

Disease associations

DepressionAnxiety disorderAttention-deficit/hyperactivity disorder (ADHD)Obsessive-compulsive disorderSubstance-use disorder / addictionParkinson’s diseaseAutism spectrum disorderSchizophreniaObesity
05

Safety considerations

Risk of serotonin syndromePsychostimulant side effects (e.g. insomnia, agitation, appetite suppression, abuse potential)Cardiovascular risks (hypertension, tachycardia)Withdrawal syndromesDrug-drug interactions (especially via serotonin or norepinephrine pathways)
06

Interacting drugs

Tricyclic antidepressants (TCAs, e.g. imipramine)

6 more in the full profile.

07

Biomarkers

Imaging or PET ligands for monoamine transporters (e.g., [^123I]β-CIT for DAT/SERT)Monoamine metabolite levels in cerebrospinal fluid (CSF) or plasma, but clinical use is limited

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