Journal article
Glycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain
Nature Reviews Drug Discovery, Vol.12(11), pp.866-885
2013
Abstract
Glycine transporters are endogenous regulators of the dual functions of glycine, which acts as a classical inhibitory neurotransmitter at glycinergic synapses and as a modulator of neuronal excitation mediated by NMDA (N-methyl-D-aspartate) receptors at glutamatergic synapses. The two major subtypes of glycine transporters, GlyT1 and GlyT2, have been linked to the pathogenesis and/or treatment of central and peripheral nervous system disorders, including schizophrenia and related affective and cognitive disturbances, alcohol dependence, pain, epilepsy, breathing disorders and startle disease (also known as hyperekplexia). This Review examines the rationale for the therapeutic potential of GlyT1 and GlyT2 inhibition, and surveys the latest advances in the biology of glycine reuptake and transport as well as the drug discovery and clinical development of compounds that block glycine transporters. © 2013 Macmillan Publishers Limited. All rights reserved.
Details
- Title
- Glycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain
- Authors
- Robert J Harvey (Author) - University College London, United KingdomB K Yee (Author) - Legacy Research Institute, United States
- Publication details
- Nature Reviews Drug Discovery, Vol.12(11), pp.866-885
- Publisher
- Nature Publishing Group
- Date published
- 2013
- DOI
- 10.1038/nrd3893
- ISSN
- 1474-1776
- Organisation Unit
- School of Health; University of the Sunshine Coast, Queensland; School of Health and Sport Sciences - Legacy; Centre for Bioinnovation; School of Health and Behavioural Sciences - Legacy
- Language
- English
- Record Identifier
- 99450451402621
- Output Type
- Journal article
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- International collaboration
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- Pharmacology & Pharmacy
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