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Elucidation of mu-Opioid Gene Structure: How Genetics Can Help Predict Responses to Opioids.μ-阿片类基因结构的阐释:遗传学如何助力预测对阿片类药物的反应。
Eur J Pain Suppl. 2011 Nov 11;5(2):433-438. doi: 10.1016/j.eujps.2011.08.022.
2
Expansion of the human mu-opioid receptor gene architecture: novel functional variants.人类μ-阿片受体基因结构的扩展:新型功能变体
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Synaptic Regulation by OPRM1 Variants in Reward Neurocircuitry.阿片受体μ型(OPRM1)变体对奖赏神经回路的突触调节。
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Identification of five mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.鉴定出五个含有一个新鉴定的可变剪接外显子的小鼠μ-阿片受体(MOR)基因(Oprm1)剪接变体。
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Tetrapeptide Endomorphin Analogs Require Both Full Length and Truncated Splice Variants of the Mu Opioid Receptor Gene Oprm1 for Analgesia.四肽内吗啡肽类似物的镇痛作用需要μ阿片受体基因Oprm1的全长和截短剪接变体。
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Genetic variation in the behavioral effects of buprenorphine in female mice derived from a murine model of the OPRM1 A118G polymorphism.在源自 OPRM1 A118G 多态性的小鼠模型中,女性小鼠丁丙诺啡行为效应的遗传变异。
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Truncated μ-Opioid Receptors With 6 Transmembrane Domains Are Essential for Opioid Analgesia.截断型具有 6 个跨膜结构域的 μ-阿片受体是阿片类药物镇痛所必需的。
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A6V polymorphism of the human μ-opioid receptor decreases signalling of morphine and endogenous opioids in vitro.人类μ-阿片受体的A6V多态性在体外会降低吗啡和内源性阿片类物质的信号传导。
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Buprenorphine signalling is compromised at the N40D polymorphism of the human μ opioid receptor in vitro.在体外,丁丙诺啡信号传导在人μ阿片受体的N40D多态性处受损。
Br J Pharmacol. 2014 Sep;171(18):4273-88. doi: 10.1111/bph.12785.
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Cellular signalling of non-synonymous single-nucleotide polymorphisms of the human μ-opioid receptor (OPRM1).人类μ-阿片受体(OPRM1)非同义单核苷酸多态性的细胞信号传导
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本文引用的文献

1
Diversity of opioid requirements for postoperative pain control following oral surgery--is it affected by polymorphism of the μ-opioid receptor?口腔手术后术后疼痛控制所需阿片类药物的多样性——它是否受μ-阿片受体多态性的影响?
Anesth Prog. 2010 Winter;57(4):145-9. doi: 10.2344/0003-3006-57.4.145.
2
Study of the OPRM1 A118G genetic polymorphism associated with postoperative nausea and vomiting induced by fentanyl intravenous analgesia.阿片μ受体 1 基因 A118G 多态性与芬太尼静脉镇痛术后恶心呕吐的相关性研究。
Minerva Anestesiol. 2011 Jan;77(1):33-9. Epub 2010 Dec 9.
3
Human opioid μ-receptor A118G polymorphism may protect against central pruritus by epidural morphine for post-cesarean analgesia.人类阿片μ受体 A118G 多态性可能通过硬膜外吗啡预防剖宫产术后镇痛的中枢性瘙痒。
Acta Anaesthesiol Scand. 2010 Nov;54(10):1265-9. doi: 10.1111/j.1399-6576.2010.02310.x.
4
The μ-opioid receptor variant N190K is unresponsive to peptide agonists yet can be rescued by small-molecule drugs.μ-阿片受体变异体 N190K 对肽类激动剂无反应,但可以被小分子药物挽救。
Mol Pharmacol. 2010 Nov;78(5):837-45. doi: 10.1124/mol.110.064188. Epub 2010 Aug 11.
5
A novel alternatively spliced isoform of the mu-opioid receptor: functional antagonism.一种新型的μ阿片受体剪接异构体:功能拮抗。
Mol Pain. 2010 Jun 2;6:33. doi: 10.1186/1744-8069-6-33.
6
Association of human micro-opioid receptor gene polymorphism A118G with fentanyl analgesia consumption in Chinese gynaecological patients.人类μ-阿片受体基因 A118G 多态性与中国妇科患者芬太尼镇痛消耗的关联。
Anaesthesia. 2010 Feb;65(2):130-5. doi: 10.1111/j.1365-2044.2009.06193.x. Epub 2009 Dec 9.
7
Mu-opioid receptor (A118G) single-nucleotide polymorphism affects alfentanil requirements for extracorporeal shock wave lithotripsy: a pharmacokinetic-pharmacodynamic study.μ-阿片受体(A118G)单核苷酸多态性影响体外冲击波碎石术所需的阿芬太尼剂量:一项药代动力学-药效学研究。
Br J Anaesth. 2009 Sep;103(3):420-7. doi: 10.1093/bja/aep192. Epub 2009 Jul 15.
8
Ethnicity and OPRM variant independently predict pain perception and patient-controlled analgesia usage for post-operative pain.种族和OPRM基因变异独立预测术后疼痛的疼痛感知和患者自控镇痛的使用情况。
Mol Pain. 2009 Jun 23;5:32. doi: 10.1186/1744-8069-5-32.
9
Functional characterization of human variants of the mu-opioid receptor gene.μ-阿片受体基因人类变体的功能特性
Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10811-6. doi: 10.1073/pnas.0904509106. Epub 2009 Jun 15.
10
Expansion of the human mu-opioid receptor gene architecture: novel functional variants.人类μ-阿片受体基因结构的扩展:新型功能变体
Hum Mol Genet. 2009 Mar 15;18(6):1037-51. doi: 10.1093/hmg/ddn439. Epub 2008 Dec 22.

μ-阿片类基因结构的阐释:遗传学如何助力预测对阿片类药物的反应。

Elucidation of mu-Opioid Gene Structure: How Genetics Can Help Predict Responses to Opioids.

作者信息

Diatchenko Luda, Robinson J Elliott, Maixner William

机构信息

Centre for Neurosensory Disorders, University of North Carolina at Chapel Hill, Chapel Hill, USA.

出版信息

Eur J Pain Suppl. 2011 Nov 11;5(2):433-438. doi: 10.1016/j.eujps.2011.08.022.

DOI:10.1016/j.eujps.2011.08.022
PMID:22102848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3217294/
Abstract

Opioid drugs are among the most commonly used and effective human analgesics. To date, the clinical benefits of opioid analgesics have not been fully realized due to substantial individual variations in the responses to opioids, insufficient drug dosing, and a high rate (up to 66%) of adverse events. As such, there is a substantial need to identify the genetic and molecular biological mechanisms that mediate individual responses to opioid therapy. Recent discoveries show that genetic variations in the μ-opioid receptor (OPRM1) gene locus play an essential role in inter-individual responses. The majority of genetic association studies have focused on the A118G polymorphism, which codes for a non-synonymous change in OPRM1 exon 1. In addition to the A118G polymorphism, another functional SNP (rs563649), which is located within an alternatively-spliced OPRM1 isoform (MOR-1K), has been identified. The MOR-1k isoform codes for 6TM OPRM1 isoforms that display excitatory rather than the inhibitory cellular effects, which are characteristic of the canonical 7TM isoforms. Thus, stimulation of the 6TM isoforms may engage the molecular mechanisms mediating opioid-dependent hyperalgesia, tolerance and dependence. Future clinical and basic studies that seek to identify the functional genetic variants within OPRM1 locus, and associated molecular mechanisms, will result in a better understanding of individual responses to opioid therapy and ultimately to the development new pharmacotherapeutics and diagnostic tools.

摘要

阿片类药物是最常用且有效的人类镇痛药之一。迄今为止,由于个体对阿片类药物的反应存在显著差异、药物剂量不足以及高发生率(高达66%)的不良事件,阿片类镇痛药的临床益处尚未得到充分实现。因此,迫切需要确定介导个体对阿片类药物治疗反应的遗传和分子生物学机制。最近的发现表明,μ-阿片受体(OPRM1)基因座的遗传变异在个体间反应中起重要作用。大多数基因关联研究都集中在A118G多态性上,该多态性编码OPRM1外显子1中的非同义变化。除了A118G多态性外,另一个功能性单核苷酸多态性(rs563649)已被确定,它位于可变剪接的OPRM1异构体(MOR-1K)内。MOR-1K异构体编码6TM OPRM1异构体,其表现出兴奋性而非典型7TM异构体特有的抑制性细胞效应。因此,刺激6TM异构体可能涉及介导阿片类药物依赖性痛觉过敏、耐受性和依赖性的分子机制。未来旨在确定OPRM1基因座内功能性遗传变异及其相关分子机制的临床和基础研究,将有助于更好地理解个体对阿片类药物治疗的反应,并最终推动新型药物治疗和诊断工具的开发。