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Br J Pharmacol. 2021 Feb;178(4):933-945. doi: 10.1111/bph.15335. Epub 2021 Jan 4.
2
A breeding strategy to identify modifiers of high genetic risk for methamphetamine intake.一种用于鉴定苯丙胺摄入高遗传风险修饰因子的育种策略。
Genes Brain Behav. 2021 Feb;20(2):e12667. doi: 10.1111/gbb.12667. Epub 2020 Jun 17.
3
Effects of a trace amine-associated receptor 1 agonist RO 5263397 on ethanol-induced behavioral sensitization.痕量胺相关受体 1 激动剂 RO 5263397 对乙醇诱导的行为敏化的影响。
Behav Brain Res. 2020 Jul 15;390:112641. doi: 10.1016/j.bbr.2020.112641. Epub 2020 May 12.
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A Non-D2-Receptor-Binding Drug for the Treatment of Schizophrenia.一种用于治疗精神分裂症的非 D2 受体结合药物。
N Engl J Med. 2020 Apr 16;382(16):1497-1506. doi: 10.1056/NEJMoa1911772.
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TAAR1 agonists attenuate extended-access cocaine self-administration and yohimbine-induced reinstatement of cocaine-seeking.TAAR1激动剂可减轻长期获取可卡因的自我给药行为以及育亨宾诱导的可卡因觅药行为恢复。
Br J Pharmacol. 2020 Aug;177(15):3403-3414. doi: 10.1111/bph.15061. Epub 2020 May 5.
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Amphetamine Stimulates Endocytosis of the Norepinephrine and Neuronal Glutamate Transporters in Cultured Locus Coeruleus Neurons.安非他命刺激培养的蓝斑神经元中去甲肾上腺素和神经元谷氨酸转运体的内吞作用。
Neurochem Res. 2020 Jun;45(6):1410-1419. doi: 10.1007/s11064-019-02939-6. Epub 2020 Jan 7.
7
Trace amine-associated receptor gene polymorphism increases drug craving in individuals with methamphetamine dependence.痕胺相关受体基因多态性增加了甲基苯丙胺依赖个体的药物渴求。
PLoS One. 2019 Oct 10;14(10):e0220270. doi: 10.1371/journal.pone.0220270. eCollection 2019.
8
Amphetamines signal through intracellular TAAR1 receptors coupled to Gα and Gα in discrete subcellular domains.安非他命通过与Gα和Gα偶联的细胞内TAAR1受体在离散的亚细胞结构域中发出信号。
Mol Psychiatry. 2021 Apr;26(4):1208-1223. doi: 10.1038/s41380-019-0469-2. Epub 2019 Aug 9.
9
gene variants have a causal role in methamphetamine intake and response and interact with .基因变异在冰毒摄入和反应中起因果作用,并与. 相互作用。
Elife. 2019 Jul 9;8:e46472. doi: 10.7554/eLife.46472.
10
Trace Amines and Their Receptors.痕量胺及其受体
Pharmacol Rev. 2018 Jul;70(3):549-620. doi: 10.1124/pr.117.015305.

痕量胺相关受体 1 与药物滥用。

Trace amine-associated receptor 1 and drug abuse.

机构信息

Medical College of Yangzhou University, Yangzhou, China; Department of Pharmacology and Toxicology, University at Buffalo, Buffalo, NY, United States.

Department of Psychological and Brain Sciences, College of Liberal Arts, Texas A&M University, College Station, TX, United States.

出版信息

Adv Pharmacol. 2022;93:373-401. doi: 10.1016/bs.apha.2021.10.005. Epub 2021 Nov 11.

DOI:10.1016/bs.apha.2021.10.005
PMID:35341572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9826737/
Abstract

Trace amine-associated receptor 1 (TAAR1) is the best characterized receptor selectively activated by trace amines. It is broadly expressed in the monoaminergic system in the brain including ventral tegmental area (VTA), nucleus accumbens (NAc), dorsal raphe (DR) and substantial nigra (SN). Extensive studies have suggested that TAAR1 plays an important role in the modulation of monoaminergic system, especially dopamine (DA) transmission which may underlie the mechanisms by which TAAR1 interventions affect drug abuse-like behaviors. TAAR1 activation inhibits the rewarding and reinforcing effects of drugs from different classes including psychostimulants, opioid and alcohol as well as drug-induced increase in DA accumulation. The mechanisms of TAAR1's function in mediating drug abuse-like behaviors are not clear. However, it is hypothesized that TAAR1 interaction with DA transporter (DAT) and dopamine D2 receptor (D2) and the subsequent modulation of cellular cascades may contribute to the effects of TAAR1 in regulating drug abuse. Further studies are needed to investigate the role of TAAR1 in other drugs of abuse-related behaviors and its safety and efficacy for prolonged medications. Together, TAAR1 inhibits drug-induced DA transmission and drug abuse-related behaviors. Therefore, TAAR1 may be a promising therapeutic target for the treatment of drug addiction.

摘要

痕量胺相关受体 1(TAAR1)是被痕量胺选择性激活的研究最为透彻的受体。它在大脑的单胺能系统中广泛表达,包括腹侧被盖区(VTA)、伏隔核(NAc)、中缝背核(DR)和黑质致密部(SN)。大量研究表明,TAAR1 在调节单胺能系统中发挥着重要作用,特别是多巴胺(DA)传递,这可能是 TAAR1 干预影响类似药物滥用行为的机制基础。TAAR1 的激活抑制了来自不同类别的药物的奖赏和强化作用,包括精神兴奋剂、阿片类药物和酒精,以及药物诱导的 DA 积累增加。TAAR1 介导类似药物滥用行为的功能机制尚不清楚。然而,有人假设 TAAR1 与多巴胺转运蛋白(DAT)和多巴胺 D2 受体(D2)的相互作用以及随后的细胞级联的调节可能有助于 TAAR1 调节药物滥用的作用。需要进一步的研究来调查 TAAR1 在其他与滥用药物相关的行为中的作用及其在长期用药中的安全性和疗效。总之,TAAR1 抑制药物诱导的 DA 传递和与药物滥用相关的行为。因此,TAAR1 可能是治疗药物成瘾的有前途的治疗靶点。