Abstract
G protein-coupled dopamine receptors (D1, D2, D3, D4, and D5) mediate all of the physiological functions of the catecholaminergic neurotransmitter dopamine, ranging from voluntary movement and reward to hormonal regulation and hypertension. Pharmacological agents targeting dopaminergic neurotransmission have been clinically used in the management of several neurological and psychiatric disorders, including Parkinson's disease, schizophrenia, bipolar disorder, Huntington's disease, attention deficit hyperactivity disorder (ADHD1), and Tourette's syndrome. Numerous advances have occurred in understanding the general structural, biochemical, and functional properties of dopamine receptors that have led to the development of multiple pharmacologically active compounds that directly target dopamine receptors, such as antiparkinson drugs and antipsychotics. Recent progress in understanding the complex biology of dopamine receptor-related signal transduction mechanisms has revealed that, in addition to their primary action on cAMP-mediated signaling, dopamine receptors can act through diverse signaling mechanisms that involve alternative G protein coupling or through G protein-independent mechanisms via interactions with ion channels or proteins that are characteristically implicated in receptor desensitization, such as β-arrestins. One of the future directions in managing dopamine-related pathologic conditions may involve a transition from the approaches that directly affect receptor function to a precise targeting of postreceptor intracellular signaling modalities either directly or through ligand-biased signaling pharmacology. In this comprehensive review, we discuss dopamine receptor classification, their basic structural and genetic organization, their distribution and functions in the brain and the periphery, and their regulation and signal transduction mechanisms. In addition, we discuss the abnormalities of dopamine receptor expression, function, and signaling that are documented in human disorders and the current pharmacology and emerging trends in the development of novel therapeutic agents that act at dopamine receptors and/or on related signaling events.
Footnotes
J.M.B. and R.R.G. contributed equally to this work.
This article is available online at http://pharmrev.aspetjournals.org.
doi:10.1124/pr.110.002642.
↵1 Abbreviations:
- AC
- adenylate cyclase
- ACR16
- huntexil
- ADHD
- attention deficit hyperactivity disorder
- AMPA
- α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
- BAC
- bacterial artificial chromosome
- BDNF
- brain-derived neurotrophic factor
- CDK5
- cyclin-dependent kinase 5
- CK
- casein kinase
- CREB
- cAMP response element-binding protein
- D2L
- D2-long
- D2S
- D2-short
- DAG
- diacylglycerol
- DARPP-32
- 32-kDa dopamine and cAMP-regulated phosphoprotein
- DAT
- dopamine transporter
- Epac
- exchange proteins directly activated by cAMP
- ERK
- extracellular-signal regulated kinase 1 and 2
- GIRK
- G protein-coupled inwardly rectifying potassium channel
- GPCR
- G protein-coupled receptor
- GRK
- G protein-coupled receptor kinase
- GSK-3
- glycogen synthase kinase 3
- HEK
- human embryonic kidney
- IP3
- inositol trisphosphate
- KO
- knockout
- LTD
- long-term depression
- MAP
- mitogen-activated protein
- MEK
- MAP/ERK kinase
- MK-801
- dizocilpine maleate
- MSN
- medium spiny neuron
- NCS-1
- neuronal calcium sensor-1
- NMDA
- N-methyl-d-aspartate
- OSU6162
- (3S)-3-[3-(methylsulfonyl)phenyl]-1-propylpiperidine hydrochloride
- Par-4
- prostate apoptosis response-4
- PD
- Parkinson's disease
- PKA
- protein kinase A
- PKC
- protein kinase C
- PLC
- phospholipase C
- PP1
- protein phosphatase 1
- PP2A
- protein phosphatase 2A
- PP2B
- protein phosphatase 2B
- PSD-95
- postsynaptic density-95
- RGS
- regulators of G protein signaling
- SCH23390
- 7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
- SL327
- α-[amino[(4-aminophenyl)thio]methylene]-2-(trifluoromethyl)benzeneacetonitrile
- STEP
- striatal-enriched tyrosine phosphatase
- WT
- wild type.
- © 2011 by The American Society for Pharmacology and Experimental Therapeutics
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