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    Dopamine receptor D3

    From Wikipedia - Reading time: 15 min
    DRD3
    Available structures
    PDBOrtholog search: PDBe RCSB
    Identifiers
    AliasesDRD3, D3DR, ETM1, FET1, dopamine receptor D3
    External IDsOMIM: 126451; MGI: 94925; HomoloGene: 623; GeneCards: DRD3; OMA:DRD3 - orthologs
    Orthologs
    SpeciesHumanMouse
    Entrez

    1814

    13490

    Ensembl

    ENSG00000151577

    ENSMUSG00000022705

    UniProt

    P35462

    P30728

    RefSeq (mRNA)

    NM_007877

    RefSeq (protein)

    NP_000787
    NP_001269492
    NP_001277738
    NP_387512

    NP_031903

    Location (UCSC)Chr 3: 114.13 – 114.2 MbChr 16: 43.57 – 43.64 Mb
    PubMed search[3][4]
    Wikidata
    View/Edit HumanView/Edit Mouse

    Dopamine receptor D3 is a protein that in humans is encoded by the DRD3 gene.[5][6]

    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.[citation needed] It is a target for drugs which treat schizophrenia, drug addiction, and Parkinson's disease.[7] 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).[6]

    Function

    [edit]

    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.[8][9]

    D3 agonists like 7-OH-DPAT, pramipexole, and rotigotine, among others, display antidepressant effects in rodent models of depression.[10][11] Apomorphine has the ability to help PD patients with their cognition awareness.[12] 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.[13][14]

    Animal studies

    [edit]

    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.[15][16][17] In contrast, D3-preferring antagonists have antipsychotic-like profiles in measures of PPI in rats.[18]

    Ligands

    [edit]

    Agonists

    [edit]
    • trans-N-{4-[4-(2,3-Dichlorophenyl)-1-piperazinyl]cyclohexyl}-3-methoxybenzamide, full agonist, > 200-fold binding selectivity over D4, D2, 5-HT1A, and α1-receptors[19]
    • (-)-7-{[2-(4-Phenylpiperazin-1-yl)ethyl]propylamino}-5,6,7,8-tetrahydronaphthalen-2-ol[20]
    • 5-OH-DPAT
    • 7-OH-DPAT
    • Pergolide[21]
    • 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
    • Aripiprazole (non-selective full agonist)
    • CJ-1639[22]
    • compound R,R-16: 250x binding selectivity over D2[23]
    • Dopamine (endogenous agonist)
    • ES609
    • FAUC 54
    • FAUC 73
    • PD-128,907
    • PF-219,061 (extremely selective) [24]
    • PF-592,379[25]
    • Piribedil[26] (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

    [edit]
    • BP-897[27]
    • Brexpiprazole (non-selective)
    • Buspirone (non-selective)
    • Cariprazine
    • CJB 090
    • CJ-1037 (extremely selective) [28]
    • FAUC 460 (highly selective) [29]
    • FAUC 346 (highly selective)[30]
    • Pardoprunox (non-selective)
    • Roxindole (possibly a partial agonist at the D3 autoreceptors, non-selective)
    • OS-3-106
    • UH-232
    • WW-III-55

    Antagonists

    [edit]
    • Most Antipsychotics
    • Amisulpride (non-selective)
    • Buspirone
    • Cyproheptadine (non-selective)
    • PG 01037 [31][32]
    • Domperidone (peripheral D2 and D3 antagonist)
    • FAUC 365, silent antagonist, subtype selective[30]
    • 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[33]
    • Nafadotride
    • NGB-2904[34]
    • 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

    [edit]

    Dopamine receptor D3 has been shown to interact with CLIC6[35] and EPB41L1.[36]

    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.[37][38][39][40]

    See also

    [edit]
    • Dopamine receptor

    References

    [edit]
    1. ^ a b c GRCh38: Ensembl release 89: ENSG00000151577 – Ensembl, May 2017
    2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022705 – Ensembl, May 2017
    3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
    4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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    10. ^ Breuer ME, Groenink L, Oosting RS, Buerger E, Korte M, Ferger B, Olivier B (August 2009). "Antidepressant effects of pramipexole, a dopamine D3/D2 receptor agonist, and 7-OH-DPAT, a dopamine D3 receptor agonist, in olfactory bulbectomized rats". European Journal of Pharmacology. 616 (1–3): 134–140. doi:10.1016/j.ejphar.2009.06.029. PMID 19549514.
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    Further reading

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    [edit]

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