Structural Insights Accelerate the Discovery of Opioid Alternatives

被引:37
作者
Che, Tao [1 ,2 ,3 ]
Roth, Bryan L. [4 ]
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[2] Univ Hlth Sci & Pharm, Ctr Clin Pharmacol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, St Louis, MO 63110 USA
[4] Univ N Carolina, Sch Med, Dept Pharmacol, Chapel Hill, NC 27599 USA
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 90, 2021 | 2021年 / 90卷
基金
美国国家卫生研究院;
关键词
GPCR; opioid receptor; analgesic; side effects; opioids; nonopioid; POSITIVE ALLOSTERIC MODULATORS; RECEPTOR-MEDIATED INHIBITION; IRRITABLE-BOWEL-SYNDROME; BETA-ARRESTIN; BIASED AGONIST; FUNCTIONAL EXPRESSION; MOLECULAR-CLONING; CRYSTAL-STRUCTURE; OPIATE RECEPTOR; UNITED-STATES;
D O I
10.1146/annurev-biochem-061620-044044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Opioids such as morphine and oxycodone are analgesics frequently prescribed for the treatment of moderate or severe pain. Unfortunately, these medications are associated with exceptionally high abuse potentials and often cause fatal side effects, mainly through the mu-opioid receptor (MOR). Efforts to discover novel, safer, and more efficacious analgesics targeting MOR have encountered challenges. In this review, we summarize alternative strategies and targets that could be used to develop safer nonopioid analgesics. A molecular understanding of G protein-coupled receptor activation and signaling has illuminated not only the complexities of receptor pharmacology but also the potential for pathway-selective agonists and allosteric modulators as safer medications. The availability of structures of pain-related receptors, in combination with high-throughput computational tools, has accelerated the discovery of multitarget ligands with promising pharmacological profiles. Emerging clinical evidence also supports the notion that drugs targeting peripheral opioid receptors have potential as improved analgesic agents.
引用
收藏
页码:739 / 761
页数:23
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