Organic Cation Transporters in Psychiatric Disorders.

Antidepressant Anxiety Autism spectrum disorder Depression Dopamine Dopamine transporter Norepinephrine Norepinephrine transporter Organic cation transporter Plasma membrane monoamine transporter Psychiatric disorder Serotonin Serotonin transporter

Journal

Handbook of experimental pharmacology
ISSN: 0171-2004
Titre abrégé: Handb Exp Pharmacol
Pays: Germany
ID NLM: 7902231

Informations de publication

Date de publication:
2021
Historique:
pubmed: 21 7 2021
medline: 29 10 2021
entrez: 20 7 2021
Statut: ppublish

Résumé

Selective serotonin reuptake inhibitors (SSRIs) are the most commonly prescribed medications for psychiatric disorders, yet they leave the majority of patients without full symptom relief. Therefore, a major research challenge is to identify novel targets for the improved treatment of these disorders. SSRIs act by blocking the serotonin transporter (SERT), the high-affinity, low-capacity, uptake-1 transporter for serotonin. Other classes of antidepressant work by blocking the norepinephrine or dopamine transporters (NET and DAT), the high-affinity, low-capacity uptake-1 transporters for norepinephrine and dopamine, or by blocking combinations of SERT, NET, and DAT. It has been proposed that uptake-2 transporters, which include organic cation transporters (OCTs) and the plasma membrane monoamine transporter (PMAT), undermine the therapeutic utility of uptake-1 acting antidepressants. Uptake-2 transporters for monoamines have low affinity for these neurotransmitters, but a high capacity to transport them. Thus, activity of these transporters may limit the increase of extracellular monoamines thought to be essential for ultimate therapeutic benefit. Here preclinical evidence supporting a role for OCT2, OCT3, and PMAT in behaviors relevant to psychiatric disorders is presented. Importantly, preclinical evidence revealing these transporters as targets for the development of novel therapeutics for psychiatric disorders is discussed.

Identifiants

pubmed: 34282486
doi: 10.1007/164_2021_473
pmc: PMC9281871
mid: NIHMS1822068
doi:

Substances chimiques

Antidepressive Agents 0
Cations 0
Dopamine Plasma Membrane Transport Proteins 0
Organic Cation Transport Proteins 0
Serotonin Plasma Membrane Transport Proteins 0
Serotonin Uptake Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

215-239

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH093320
Pays : United States

Informations de copyright

© 2021. The Author(s), under exclusive license to Springer Nature Switzerland AG.

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Auteurs

Lynette C Daws (LC)

Departments of Cellular and Integrative Physiology, and Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA. daws@uthscsa.edu.

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Classifications MeSH