User:Panintelize/沙盒7
| Trace amine associated receptor 1 | |||
|---|---|---|---|
| 标识 | |||
| 代号 | TAAR1; TA1; TAR1; TRAR1 | ||
| 扩展标识 | 遗传学：609333 鼠基因：2148258 同源基因：24938 IUPHAR: TA1 ChEMBL: 5857 GeneCards: TAAR1 Gene | ||
| RNA表达模式 | |||
 | |||
| 更多表达数据 | |||
| 直系同源体 | |||
| 物种 | 人类 | 小鼠 | |
| Entrez | 134864 | 111174 | |
| Ensembl | ENSG00000146399 | ENSMUSG00000056379 | |
| UniProt | Q96RJ0 | Q923Y8 | |
| mRNA序列 | NM_138327 | NM_053205 | |
| 蛋白序列 | NP_612200 | NP_444435 | |
| 基因位置 |
Chr 6: 132.64 – 132.65 Mb |
Chr 10: 23.92 – 23.92 Mb | |
| PubMed查询 | [1] | [2] | |
Trace amine-associated receptor 1 (TAAR1) is a protein that in humans is encoded by the TAAR1 gene.[1] TAAR1 is an amine-activated Gs-coupled and Gq-coupled G protein-coupled receptor (GPCR) that is primarily located in several peripheral organs, lymphocytes, astrocytes, and in the intracellular compartments within the presynaptic plasma membrane (i.e., axon terminal) of monoamine neurons in the central nervous system (CNS).[2][3][4] TAAR1 was discovered in 2001 by two independent groups of investigators, Borowski et al. and Bunzow et al.[5][6] TAAR1 is one of six functional trace amine-associated receptors in humans, which are so named for their ability to bind endogenous amines that occur in tissues at trace concentrations.[7][8] TAAR1 plays a significant role in regulating neurotransmission in dopamine, norepinephrine, and serotonin neurons in the CNS;[7][3] it also affects immune system and neuroimmune system function through different mechanisms.[9][10][11][12]
The primary endogenous ligands of the human TAAR1 receptor, by rank order of potency, are:
tyramine > β-phenethylamine > dopamine = octopamine.[2]
Discovery 编辑
TAAR1 was discovered independently by Borowski et al. and Bunzow et al. in 2001. To find the genetic variants responsible for TAAR1 synthesis, they used mixtures of oligonucleotides with sequences related to G protein-coupled receptors (GPCRs) of serotonin and dopamine to discover novel DNA sequences in rat genomic DNA and cDNA, which they then amplified and cloned. The resulting sequence was not found in any database and coded for TAAR1.[5][6]
Structure 编辑
TAAR1 shares structural similarities with the class A rhodopsin GPCR subfamily.[6] It has 7 transmembrane domains with short N and C terminal extensions.[13] TAAR1 is 62–96% identical with TAARs2-15, which suggests that the TAAR subfamily has recently evolved; while at the same time, the low degree of similarity between TAAR1 orthologues suggests that they are rapidly evolving.[5] TAAR1 shares a predictive peptide motif with all other TAARs. This motif overlaps with transmembrane domain VII, and its identity is NSXXNPXX[Y,H]XXX[Y,F]XWF. TAAR1 and its homologues have ligand pocket vectors that utilize a sets of 35 amino acids known to be involved directly in receptor-ligand interaction.[8]
Gene 编辑
All TAAR genes are located on a single chromosome spanning 109kb of human chromosome 6q23.1, 192 kb of mouse chromosome 10A4, and 216 kb of rat chromosome 1p12. Each TAAR is derived from a single exon, except for TAAR2, which is coded by two exons.[8]
Tissue distribution 编辑
To date, TAAR1 has been identified and cloned in four different mammal genomes: human, mouse, rat, monkey, and chimpanzee. In rats, mRNA for TAAR1 is found at low to moderate levels in peripheral tissues like the stomach, kidney, and lungs, and at low levels in the brain amygdala.[5] Rhesus monkey Taar1 and human TAAR1 (hTAAR1) share high sequence similarity, and TAAR1 mRNA is highly expressed in the same important monoaminergic regions of both species. These regions include the dorsal and ventral caudate nucleus, putamen, substantia nigra, nucleus accumbens, ventral tegmental area, locus coeruleus, amygdala, and raphe nucleus.[2][14] TAAR1 has also been identified in human astrocytes.[2][9]
TAAR1 is the only TAAR subtype not found in the olfactory epithelium.[15]
Location within neurons 编辑
Human TAAR1 is an intracellular receptor expressed within the presynaptic terminal of monoamine neurons;[7][3][16] in model cell systems, hTAAR1 has extremely poor membrane expression.[16] A method to induce hTAAR1 membrane expression has been used to study its pharmacology via a bioluminescence resonance energy transfer cAMP assay.[16]
Because TAAR1 is an intracellular receptor in monoamine neurons, TAAR1 ligands must enter the presynaptic neuron through a membrane transport protein[note 1] or be able to diffuse across the presynaptic membrane in order to reach the receptor and produce reuptake inhibition and neurotransmitter efflux.[7] Consequently, the efficacy of a particular TAAR1 ligand in producing these effects in different monoamine neurons is a function of both its binding affinity at TAAR1 and its capacity to move across the presynaptic membrane at each type of neuron.[7] The variability between a TAAR1 ligand's substrate affinity at the various monoamine transporters accounts for much of the difference in its capacity to produce neurotransmitter release and reuptake inhibition in different types of monoamine neurons.[7] E.g., a TAAR1 ligand which can easily pass through the norepinephrine transporter, but not the serotonin transporter, will produce – all else equal – markedly greater TAAR1-induced effects in norepinephrine neurons as compared to serotonin neurons.
Receptor oligomers 编辑
TAAR1 forms GPCR oligomers with monoamine autoreceptors in neurons in vivo.[17][18] These hetero-oligomers include:
Ligands 编辑
Agonists 编辑
Trace amines 编辑
Trace amines are those found in 0.1–10 nM concentrations, constituting less than 1% of total biogenic amines in the mammalian nervous system.[20] Some of the endogenous human trace amines include para/meta-tyramine, tryptamine, phenylethylamine (PEA), and para/meta-octopamine. These share structural similarities with the three common monoamines: serotonin, dopamine, and norepinephrine. Each ligand has a different potency, measured as increases cyclic AMP (cAMP) concentration after the binding event. The rank order of potency for the primary endogenous ligands at hTAAR1 is:
tyramine > β-phenethylamine > dopamine = octopamine.[2]
Thyronamines 编辑
Thyronamines are molecular derivatives of the thyroid hormone and are very important for endocrine system function. 3-Iodothyronamine (T1AM) is the most potent TAAR1 agonist yet discovered, although it lacks monoamine transporter affinity and therefore has little effect in monoamine neurons of the central nervous system. Activation of TAAR1 by T1AM results in the production of large amounts of cAMP. This effect is coupled with decreased body temperature and cardiac output.
Synthetic 编辑
- Amphetamine and the amphetamine-related compounds methamphetamine, 3,4-methylenedioxymethamphetamine (MDMA), and 2,5-dimethoxy-4-iodoamphetamine (DOI) are all potent rTAAR1 agonists. Upon association with TAAR1, they elicit increases in cAMP production similar to those of PEA and p-tyramine. Not surprisingly, these amphetamine-like compounds are structurally similar to PEA and p-tyramine.[6][21]
- Benzofurans: 5-APB, 5-APDB, 6-APB, 6-APDB, 4-APB, 7-APB, 5-EAPB, and 5-MAPDB, as well as the benzodifuran 2C-B-FLY, are hTAAR1 agonists that have an MDMA-like pharmacodynamic profile.[22]
- The methylphenethylamines are agonists of hTAAR1; these include α-methylphenethylamine, β-methylphenethylamine, N-methylphenethylamine (not synthetic), 2-methylphenethylamine, 3-methylphenethylamine, and 4-methylphenethylamine.[23]
- In rats, lysergic acid diethylamide (LSD) is an agonist,[6] but it lacks any affinity for human TAAR1.[23]
- RO5166017 or (S)-4-[(ethylphenylamino)methyl]-4,5-dihydrooxazol-2-ylamine is a selective TAAR1 agonist without significant activity at other targets.[24]
- RO5203648 and RO5263397 are highly selective TAAR1 partial agonists.[17] RO5203648 demonstrated clear antidepressant and anti-psychotic activity, additionally it attenuated drug self-administration and exhibited wakefulness promoting and cognition enhancing properties in murine and simian models.[25]
Antagonists 编辑
Function 编辑
Phenethylamine and amphetamine in a TAAR1-localized dopamine neuron
 |
Monoaminergic systems 编辑
Before the discovery of TAAR1, trace amines were believed to serve very limited functions. They were thought to induce noradrenaline release from sympathetic nerve endings and compete for catecholamine or serotonin binding sites on cognate receptors, transporters, and storage sites.[20] Today, they are believed to play a much more dynamic role by regulating monoaminergic systems in the brain.
One of the downstream effects of active TAAR1 is to increase cAMP in the presynaptic cell via Gαs G-protein activation of adenylyl cyclase.[5][6][8] This alone can have a multitude of cellular consequences. A main function of the cAMP may be to up-regulate the expression of trace amines in the cell cytoplasm.[21] These amines would then activate intracellular TAAR1. Monoamine autoreceptors (e.g., D2 short, presynaptic α2, and presynaptic 5-HT1A) have the opposite effect of TAAR1, and together these receptors provide a regulatory system for monoamines.[7] Notably, amphetamine and trace amines bind to TAAR1, but not monoamine autoreceptors.[7] The effect of TAAR1 agonists on monoamine transporters in the brain appears to be site-specific.[7] Imaging studies indicate that monoamine reuptake inhibition by amphetamine and trace amines is dependent upon the presence of TAAR1 co-localization in the associated monoamine neurons.[7] As of 2010, co-localization of TAAR1 and the dopamine transporter (DAT) has been visualized in rhesus monkeys, but co-localization of TAAR1 with the norepinephrine transporter (NET) and the serotonin transporter (SERT) has only been evidenced by messenger RNA (mRNA) expression.[7]
In neurons with co-localized TAAR1, TAAR1 agonists increase the concentrations of the associated monoamines in the synaptic cleft, thereby increasing post-synaptic receptor binding.[7] Through direct activation of G protein-coupled inwardly-rectifying potassium channels (GIRKs), TAAR1 can reduce the firing rate of dopamine neurons, in turn preventing a hyper-dopaminergic state.[24][27][28] Amphetamine and trace amines can enter the presynaptic neuron either through DAT or by diffusing across the neuronal membrane directly.[7] As a consequence of DAT uptake, amphetamine and trace amines produce competitive reuptake inhibition at the transporter.[7] Upon entering the presynaptic neuron, these compounds activate TAAR1 which, through protein kinase A (PKA) and protein kinase C (PKC) signaling, causes DAT phosphorylation. Phosphorylation by either protein kinase can result in DAT internalization (non-competitive reuptake inhibition), but PKC-mediated phosphorylation alone induces reverse transporter function (dopamine efflux).[7][29]
Immune system 编辑
Expression of TAAR1 on lymphocytes is associated with activation of lymphocyte immuno-characteristics. In the immune system, TAAR1 transmits signals through active PKA and PKC phosphorylation cascades.[11] In a recent study, Panas et al. observed that methamphetamine had these effects, suggesting that, in addition to brain monoamine regulation, amphetamine-related compounds may have an effect on the immune system.[11] A recent paper showed that, along with TAAR1, TAAR2 is required for full activity of trace amines in PMN cells.[12]
Phytohaemagglutinin upregulates hTAAR1 mRNA in circulating leukocytes;[2] in these cells, TAAR1 activation mediates leukocyte chemotaxis toward TAAR1 agonists.[2] TAAR1 agonists (specifically, trace amines) have also been shown to induce interleukin 4 secretion in T-cells and immunoglobulin E (IgE) secretion in B cells.[2]
Astrocyte-localized TAAR1 regulates EAAT2 levels and function in these cells;[9] this has been implicated in methamphetamine-induced pathologies of the neuroimmune system.[9]
Clinical significance 编辑
Low phenethylamine (PEA) concentration in the brain is associated with major depressive disorder, and high concentrations are associated with schizophrenia. It is hypothesized that insufficient PEA levels result in TAAR1 inactivation and overzealous monoamine uptake by transporters, possibly resulting in depression (see "Discussion" in [5][20]). Some antidepressants function by inhibiting monoamine oxidase (MAO), which increases the concentration of trace amines, which is speculated to increase TAAR1 activation in presynaptic cells (see "Discussion" in [5][8]). Decreased PEA metabolism has been linked to schizophrenia, a logical finding considering excess PEA would result in over-activation of TAAR1 and prevention of monoamine transporter function. Interestingly, mutations in region q23.1 of human chromosome 6 – the same chromosome that codes for TAAR1 – have been linked to schizophrenia.[8]
A large candidate gene association study published in September 2011 found significant differences in TAAR1 allele frequencies between a cohort of fibromyalgia patients and a chronic pain-free control group, suggesting this gene may play an important role in the pathophysiology of the condition; this possibly presents a target for therapeutic intervention.[30]
TAAR1 activation has also been connected to activation of lymphocyte immuno-characteristics via a PKA and PKC phosphorylation.[11]
Research 编辑
Medical reviews from February 2015 and 2016 noted that TAAR1-selective ligands have significant therapeutic potential for treating psychostimulant addictions (e.g., cocaine, amphetamine, methamphetamine, etc.).[3][4]
Notes 编辑
- ^ In dopamine, norepinephrine, and serotonin neurons, the primary membrane transporters are DAT, NET, and SERT respectively.[7]
- ^ TAAR1–D2sh is a presynaptic heterodimer which involves the relocation of TAAR1 from the intracellular space to D2sh at the plasma membrane, increased D2sh agonist binding affinity, and signal transduction through the calcium–PKC–NFAT pathway and G-protein independent PKB–GSK3 pathway.[3][19]
References 编辑
- ^ Entrez Gene: TAAR1 trace amine associated receptor 1.
- ^ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Maguire JJ, Davenport AP. Trace amine receptor: TA1 receptor. IUPHAR/BPS Guide to PHARMACOLOGY. International Union of Basic and Clinical Pharmacology. 5 March 2015 [April 2015].
- ^ 3.0 3.1 3.2 3.3 3.4 Grandy DK, Miller GM, Li JX. "TAARgeting Addiction"-The Alamo Bears Witness to Another Revolution: An Overview of the Plenary Symposium of the 2015 Behavior, Biology and Chemistry Conference. Drug Alcohol Depend. February 2016, 159: 9–16. PMID 26644139. doi:10.1016/j.drugalcdep.2015.11.014.
This original observation of TAAR1 and DA D2R interaction has subsequently been confirmed and expanded upon with observations that both receptors can heterodimerize with each other under certain conditions ... Additional DA D2R/TAAR1 interactions with functional consequences are revealed by the results of experiments demonstrating that in addition to the cAMP/PKA pathway (Panas et al., 2012) stimulation of TAAR1-mediated signaling is linked to activation of the Ca++/PKC/NFAT pathway (Panas et al.,2012) and the DA D2R-coupled, G protein-independent AKT/GSK3 signaling pathway (Espinoza et al., 2015; Harmeier et al., 2015), such that concurrent TAAR1 and DA DR2R activation could result in diminished signaling in one pathway (e.g. cAMP/PKA) but retention of signaling through another (e.g., Ca++/PKC/NFA)
- ^ 4.0 4.1 Jing L, Li JX. Trace amine-associated receptor 1: A promising target for the treatment of psychostimulant addiction. Eur. J. Pharmacol. August 2015, 761: 345–352. PMID 26092759. doi:10.1016/j.ejphar.2015.06.019.
TAAR1 is largely located in the intracellular compartments both in neurons (Miller, 2011), in glial cells (Cisneros and Ghorpade, 2014) and in peripheral tissues (Grandy, 2007) ... Taken together,the data reviewed here strongly support that TAAR1 is implicated in the functional regulation of monoaminergic systems, especially dopaminergic system, and that TAAR1 serves as a homeostatic “brake” system that is involved in the modulation of dopaminergic activity. Existing data provided robust preclinical evidence supporting the development of TAAR1 agonists as potential treatment for psychostimulant abuse and addiction. ... Given that TAAR1 is primarily located in the intracellular compartments and existing TAAR1 agonists are proposed to get access to the receptors by translocation to the cell interior (Miller, 2011), future drug design and development efforts may need to take strategies of drug delivery into consideration (Rajendran et al., 2010).
- ^ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Borowsky B, Adham N, Jones KA, Raddatz R, Artymyshyn R, Ogozalek KL, Durkin MM, Lakhlani PP, Bonini JA, Pathirana S, Boyle N, Pu X, Kouranova E, Lichtblau H, Ochoa FY, Branchek TA, Gerald C. Trace amines: identification of a family of mammalian G protein-coupled receptors. Proceedings of the National Academy of Sciences of the United States of America. July 2001, 98 (16): 8966–71. PMC 55357
. PMID 11459929. doi:10.1073/pnas.151105198.
- ^ 6.0 6.1 6.2 6.3 6.4 6.5 Bunzow JR, Sonders MS, Arttamangkul S, Harrison LM, Zhang G, Quigley DI, Darland T, Suchland KL, Pasumamula S, Kennedy JL, Olson SB, Magenis RE, Amara SG, Grandy DK. Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor. Molecular Pharmacology. December 2001, 60 (6): 1181–8. PMID 11723224. doi:10.1124/mol.60.6.1181.
- ^ 7.00 7.01 7.02 7.03 7.04 7.05 7.06 7.07 7.08 7.09 7.10 7.11 7.12 7.13 7.14 7.15 Miller GM. The emerging role of trace amine-associated receptor 1 in the functional regulation of monoamine transporters and dopaminergic activity. Journal of Neurochemistry. January 2011, 116 (2): 164–76. PMC 3005101 . PMID 21073468. doi:10.1111/j.1471-4159.2010.07109.x.
- ^ 8.0 8.1 8.2 8.3 8.4 8.5 Lindemann L, Ebeling M, Kratochwil NA, Bunzow JR, Grandy DK, Hoener MC. Trace amine-associated receptors form structurally and functionally distinct subfamilies of novel G protein-coupled receptors. Genomics. March 2005, 85 (3): 372–85. PMID 15718104. doi:10.1016/j.ygeno.2004.11.010.
- ^ 9.0 9.1 9.2 9.3 Cisneros IE, Ghorpade A. Methamphetamine and HIV-1-induced neurotoxicity: role of trace amine associated receptor 1 cAMP signaling in astrocytes. Neuropharmacology. October 2014, 85: 499–507. PMID 24950453. doi:10.1016/j.neuropharm.2014.06.011.
TAAR1 overexpression significantly decreased EAAT-2 levels and glutamate clearance ... METH treatment activated TAAR1 leading to intracellular cAMP in human astrocytes and modulated glutamate clearance abilities. Furthermore, molecular alterations in astrocyte TAAR1 levels correspond to changes in astrocyte EAAT-2 levels and function.
- ^ Rogers TJ. The molecular basis for neuroimmune receptor signaling. J Neuroimmune Pharmacol. 2012, 7 (4): 722–4. PMC 4011130 . PMID 22935971. doi:10.1007/s11481-012-9398-4.
- ^ 11.0 11.1 11.2 11.3 Panas MW, Xie Z, Panas HN, Hoener MC, Vallender EJ, Miller GM. Trace amine associated receptor 1 signaling in activated lymphocytes. Journal of Neuroimmune Pharmacology. December 2012, 7 (4): 866–76. PMC 3593117 . PMID 22038157. doi:10.1007/s11481-011-9321-4.
- ^ 12.0 12.1 Babusyte A, Kotthoff M, Fiedler J, Krautwurst D. Biogenic amines activate blood leukocytes via trace amine-associated receptors TAAR1 and TAAR2. Journal of Leukocyte Biology. March 2013, 93 (3): 387–94. PMID 23315425. doi:10.1189/jlb.0912433.
- ^ Xie Z, Miller GM. Trace amine-associated receptor 1 as a monoaminergic modulator in brain. Biochemical Pharmacology. November 2009, 78 (9): 1095–104. PMC 2748138 . PMID 19482011. doi:10.1016/j.bcp.2009.05.031.
- ^ Xie Z, Westmoreland SV, Bahn ME, Chen GL, Yang H, Vallender EJ, Yao WD, Madras BK, Miller GM. Rhesus monkey trace amine-associated receptor 1 signaling: enhancement by monoamine transporters and attenuation by the D2 autoreceptor in vitro. The Journal of Pharmacology and Experimental Therapeutics. April 2007, 321 (1): 116–27. PMID 17234900. doi:10.1124/jpet.106.116863.
- ^ Liberles SD, Buck LB. A second class of chemosensory receptors in the olfactory epithelium. Nature. August 2006, 442 (7103): 645–50. PMID 16878137. doi:10.1038/nature05066.
- ^ 16.0 16.1 16.2 Barak LS, Salahpour A, Zhang X, Masri B, Sotnikova TD, Ramsey AJ, Violin JD, Lefkowitz RJ, Caron MG, Gainetdinov RR. Pharmacological characterization of membrane-expressed human trace amine-associated receptor 1 (TAAR1) by a bioluminescence resonance energy transfer cAMP biosensor. Molecular Pharmacology. September 2008, 74 (3): 585–94. PMC 3766527 . PMID 18524885. doi:10.1124/mol.108.048884.
- ^ 17.0 17.1 17.2 Lam VM, Espinoza S, Gerasimov AS, Gainetdinov RR, Salahpour A. In-vivo pharmacology of Trace-Amine Associated Receptor 1. Eur. J. Pharmacol. June 2015. PMID 26093041. doi:10.1016/j.ejphar.2015.06.026.
- ^ 18.0 18.1 Dinter J, Mühlhaus J, Jacobi SF, Wienchol CL, Cöster M, Meister J, Hoefig CS, Müller A, Köhrle J, Grüters A, Krude H, Mittag J, Schöneberg T, Kleinau G, Biebermann H. 3-iodothyronamine differentially modulates α-2A-adrenergic receptor-mediated signaling. J. Mol. Endocrinol. June 2015, 54 (3): 205–216. PMID 25878061. doi:10.1530/JME-15-0003.
Moreover, in ADRA2A/TAAR1 hetero-oligomers, the capacity of NorEpi to stimulate Gi/o signaling is reduced by co-stimulation with 3-T1AM. The present study therefore points to a complex spectrum of signaling modification mediated by 3-T1AM at different G protein-coupled receptors.
- ^ Harmeier A, Obermueller S, Meyer CA, Revel FG, Buchy D, Chaboz S, Dernick G, Wettstein JG, Iglesias A, Rolink A, Bettler B, Hoener MC. Trace amine-associated receptor 1 activation silences GSK3β signaling of TAAR1 and D2R heteromers. Eur Neuropsychopharmacol. 2015, 25 (11): 2049–61. PMID 26372541. doi:10.1016/j.euroneuro.2015.08.011.
Interaction of TAAR1 with D2R altered the subcellular localization of TAAR1 and increased D2R agonist binding affinity.
- ^ 20.0 20.1 20.2 Zucchi R, Chiellini G, Scanlan TS, Grandy DK. Trace amine-associated receptors and their ligands. British Journal of Pharmacology. December 2006, 149 (8): 967–78. PMC 2014643 . PMID 17088868. doi:10.1038/sj.bjp.0706948.
- ^ 21.0 21.1 Xie Z, Miller GM. A receptor mechanism for methamphetamine action in dopamine transporter regulation in brain. The Journal of Pharmacology and Experimental Therapeutics. July 2009, 330 (1): 316–25. PMC 2700171 . PMID 19364908. doi:10.1124/jpet.109.153775.
- ^ Rickli A, Kopf S, Hoener MC, Liechti ME. Pharmacological profile of novel psychoactive benzofurans. British Journal of Pharmacology. July 2015, 172 (13): 3412–25. PMID 25765500. doi:10.1111/bph.13128.
- ^ 23.0 23.1 Wainscott DB, Little SP, Yin T, Tu Y, Rocco VP, He JX, Nelson DL. Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1. The Journal of Pharmacology and Experimental Therapeutics. January 2007, 320 (1): 475–85. PMID 17038507. doi:10.1124/jpet.106.112532.
- ^ 24.0 24.1 Revel FG, Moreau JL, Gainetdinov RR, Bradaia A, Sotnikova TD, Mory R, Durkin S, Zbinden KG, Norcross R, Meyer CA, Metzler V, Chaboz S, Ozmen L, Trube G, Pouzet B, Bettler B, Caron MG, Wettstein JG, Hoener MC. TAAR1 activation modulates monoaminergic neurotransmission, preventing hyperdopaminergic and hypoglutamatergic activity. Proc. Natl. Acad. Sci. U.S.A. May 2011, 108 (20): 8485–90. PMC 3101002 . PMID 21525407. doi:10.1073/pnas.1103029108.
- ^ Revel FG, Moreau JL, Gainetdinov RR, Ferragud A, Velázquez-Sánchez C, Sotnikova TD, Morairty SR, Harmeier A, Groebke Zbinden K, Norcross RD, Bradaia A, Kilduff TS, Biemans B, Pouzet B, Caron MG, Canales JJ, Wallace TL, Wettstein JG, Hoener MC. Trace Amine-Associated Receptor 1 Partial Agonism Reveals Novel Paradigm for Neuropsychiatric Therapeutics. Biol Psychiatry. June 2012, 72 (11): 934–42. PMID 22705041. doi:10.1016/j.biopsych.2012.05.014.
- ^ Bradaia A, Trube G, Stalder H, Norcross RD, Ozmen L, Wettstein JG, Pinard A, Buchy D, Gassmann M, Hoener MC, Bettler B. The selective antagonist EPPTB reveals TAAR1-mediated regulatory mechanisms in dopaminergic neurons of the mesolimbic system. Proceedings of the National Academy of Sciences of the United States of America. November 2009, 106 (47): 20081–6. PMC 2785295 . PMID 19892733. doi:10.1073/pnas.0906522106.
- ^ Ledonne A, Berretta N, Davoli A, Rizzo GR, Bernardi G, Mercuri NB. Electrophysiological effects of trace amines on mesencephalic dopaminergic neurons. Frontiers in Systems Neuroscience. 2011, 5: 56. PMC 3131148 . PMID 21772817. doi:10.3389/fnsys.2011.00056.
inhibition of firing due to increased release of dopamine; (b) reduction of D2 and GABAB receptor-mediated inhibitory responses (excitatory effects due to disinhibition); and (c) a direct TA1 receptor-mediated activation of GIRK channels which produce cell membrane hyperpolarization.
- ^ 引证错误：没有为名为
Genatlas_TAAR1的参考文献提供内容 - ^ Maguire JJ, Parker WA, Foord SM, Bonner TI, Neubig RR, Davenport AP. International Union of Pharmacology. LXXII. Recommendations for trace amine receptor nomenclature. Pharmacological Reviews. March 2009, 61 (1): 1–8. PMC 2830119 . PMID 19325074. doi:10.1124/pr.109.001107.
- ^ Smith SB, Maixner DW, Fillingim RB, Slade G, Gracely RH, Ambrose K, Zaykin DV, Hyde C, John S, Tan K, Maixner W, Diatchenko L. Large candidate gene association study reveals genetic risk factors and therapeutic targets for fibromyalgia. Arthritis and Rheumatism. February 2012, 64 (2): 584–93. PMC 3237946 . PMID 21905019. doi:10.1002/art.33338.
<references>标签中name属性为“Genatlas TAAR1”的参考文献没有在文中使用
User:Panintelize/沙盒7引用了美国国家医学图书馆提供的資料，这些資料属于公共领域。
| ||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||