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Dopamine receptors –IUPHAR R eview 13
Open accessAbstract
The variety of physiological functions controlled by dopamine in the brain and periphery is mediated by the D1,D2,D3,D4 and D5 dopamine GPCRs. Drugs acting on dopamine receptors are significant tools for the management of several neuropsychiatric disorders including schizophrenia, bipolar disorder, depression and P arkinson's disease. Recent investigations of dopamine receptor signalling have shown that dopamine receptors, apart from their canonical action on cAMP‐mediated signalling, can regulate a myriad of cellular responses to fine‐tune the expression of dopamine‐associated behaviours and functions. Such signalling mechanisms may involve alternate G protein coupling or non‐G protein mechanisms involving ion channels, receptor tyrosine kinases or proteins such as β‐arrestins that are classically involved in GPCR desensitization. Another level of complexity is the growing appreciation of the physiological roles played by dopamine receptor heteromers. Applications of new in vivo techniques have significantly furthered the understanding of the physiological functions played by dopamine receptors. Here we provide an update of the current knowledge regarding the complex biology, signalling, physiology and pharmacology of dopamine receptors.
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Metadata
- Authors
- Beaulieu, J., Espinoza, S., & Gainetdinov, R. R.
- Venue
- British Journal of Pharmacology
- Publisher
- Wiley
- Published
- 2014-11-24
- Volume
- 172
- Issue
- 1
- Pages
- 1-23
- ISSN
- 0007-1188 (ISSN-L)
- 1476-5381
- OpenAlex
- W1786514222
- Cited by
- 521
- References
- 261
- FWCI
- 9.86
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.