Diatchenko Luda, Robinson J Elliott, Maixner William
Centre for Neurosensory Disorders, University of North Carolina at Chapel Hill, Chapel Hill, USA.
Eur J Pain Suppl. 2011 Nov 11;5(2):433-438. doi: 10.1016/j.eujps.2011.08.022.
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.
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。