Английская Википедия:Dopamine receptor D3

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Шаблон:Infobox gene Dopamine receptor D₃ is a protein that in humans is encoded by the DRD3 gene.

This gene encodes the D₃ subtype of the dopamine receptor. The D₃ subtype inhibits adenylyl cyclase through inhibitory G-proteins. This receptor is expressed in phylogenetically older regions of the brain, suggesting that this receptor plays a role in cognitive and emotional functions.Шаблон:Citation needed It is a target for drugs which treat schizophrenia, drug addiction, and Parkinson's disease. Alternative splicing of this gene results in multiple transcript variants that would encode different isoforms, although some variants may be subject to nonsense-mediated decay (NMD).

Function

Alpha-synuclein (α-Syn) aggregation via Lewy bodies inclusion, a pathogenic signature exclusively present in PD patients, is decreased by D3 agonists while DA content is elevated by inhibiting DA reuptake and breakdown. The regulation of α-Syn aggregation and clearance enhances brain-derived neurotrophic factor (BDNF) secretion, which ultimately ameliorates neuroinflammation and oxidative stress while promoting neurogenesis and interacting with other DA receptors.

D₃ agonists like 7-OH-DPAT, pramipexole, and rotigotine, among others, display antidepressant effects in rodent models of depression. Apomorphine has the ability to help PD patients with their cognition awareness. In addition to having antidepressant properties such as regulating the depression-like behaviors and depression development, pramipexole has the capability to prevent and slow down cell apoptosis as well as to restore damaged neural networks and connections while rotigotine help PD patients to attenuates hyperpyrexia syndrome and schizophrenia.

Animal studies

D₃ agonists have been shown to disrupt prepulse inhibition of startle (PPI), a cross-species measure that recapitulates deficits in sensorimotor gating in neuropsychiatric disorders such as schizophrenia. In contrast, D3-preferring antagonists have antipsychotic-like profiles in measures of PPI in rats.

Ligands

Agonists

• trans-N-{4-[4-(2,3-Dichlorophenyl)-1-piperazinyl]cyclohexyl}-3-methoxybenzamide, full agonist, > 200-fold binding selectivity over D₄, D₂, 5-HT_1A, and α1-receptors
• (-)-7-{[2-(4-Phenylpiperazin-1-yl)ethyl]propylamino}-5,6,7,8-tetrahydronaphthalen-2-ol
• 5-OH-DPAT
• 7-OH-DPAT
• Pergolide
• 8-OH-PBZI (cis-8-Hydroxy-3-(n-propyl)-1,2,3a,4,5,9b-hexahydro-1H-benz[e]indole)
• Apomorphine (non-selective dopamine agonist)
• Bromocriptine (non-selective dopamine agonist)
• Captodiame
• CJ-1639
• compound R,R-16: 250x binding selectivity over D₂
• Dopamine (endogenous agonist)
• ES609
• FAUC 54
• FAUC 73
• PD-128,907
• PF-219,061 (extremely selective)
• PF-592,379
• Piribedil (non-selective dopamine agonist)
• Pramipexole (non-selective dopamine agonist)
• Quinelorane (also D₂ agonist)
• Quinpirole (also D₂ agonist)
• Ropinirole (non-selective dopamine agonist)
• Rotigotine (non-selective dopamine agonist)

Partial agonists

• Aripiprazole (non-selective)
• BP-897
• Brexpiprazole (non-selective)
• Buspirone (non-selective)
• Cariprazine
• CJB 090
• CJ-1037 (extremely selective)
• FAUC 460 (highly selective)
• FAUC 346 (highly selective)
• Pardoprunox (non-selective)
• Roxindole (possibly a partial agonist at the D₃ autoreceptors, non-selective)
• OS-3-106
• UH-232
• WW-III-55

Antagonists

• Most Antipsychotics
• Amisulpride (non-selective)
• Buspirone
• Cyproheptadine (non-selective)
• PG 01037
• Domperidone (peripheral D₂ and D₃ antagonist)
• FAUC 365, silent antagonist, subtype selective
• GR-103,691
• GSK598809 (highly selective)
• Haloperidol (non-selective, blocks all dopamine receptor subtypes, though D₃ with the strongest affinity)
• N-(4-(4-(2,3-Dichloro- or 2-methoxyphenyl)piperazin-1-yl)butyl)heterobiarylcarboxamides
• Nafadotride
• NGB-2904
• PNU-99,194 (moderately selective over D₂)
• Raclopride (also D₂ antagonist)
• S-14,297 (selective)
• S33084
• SB-277011-A, selective D₃ antagonist, 80x selectivity over D₂ with no partial agonist effects, used in drug addiction research as a potential therapy for addiction to several different drugs
• SR 21502 (highly selective)
• Sulpiride (also D₂ antagonist)
• U99194
• YQA14 (high affinity and selectivity)
• Risperidone

Interactions

Dopamine receptor D₃ has been shown to interact with CLIC6 and EPB41L1.

DRD3 Ser9Gly polymorphism(rs6280), which is a single nucleotide polymorphism (SNP) with variant base C/T is linked to variation in PD such as depression severity, impulse control disorders, behavioral addiction and aberrant decision-making.

See also

• Dopamine receptor

Further reading

• Шаблон:Cite journal
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External links

• Шаблон:Cite web
• Шаблон:MeshName