Biased Agonism as an Emerging Strategy in the Search for Better Opioid Analgesics

被引:12
|
作者
Piekielna-Ciesielska, Justyna [1 ]
Wtorek, Karol [1 ]
Janecka, Anna [1 ]
机构
[1] Med Univ Lodz, Dept Biomol Chem, Mazowiecka 6-8, PL-92215 Lodz, Poland
关键词
Opioid receptors; opioid peptides; antinociceptive activity; biased agonism; bias factor; morphine; MU-AGONIST/DELTA-ANTAGONIST; ENDOMORPHIN ANALOGS; RECEPTOR AGONIST; FUNCTIONAL SELECTIVITY; TOLERANCE; LIGANDS; POTENT; PAIN; EXPRESSION; DISCOVERY;
D O I
10.2174/0929867326666190506103124
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
Morphine and related drugs that act through activating opioid receptors are the most effective analgesics for the relief of severe pain. They have been used for decades, despite the range of unwanted side effects that they produce, as no alternative has been found so far. The major goal of opioid research is to understand the mechanism of action of opioid receptor agonists and to improve the therapeutic utility of opioid drugs. In the search for safer and more potent analgesics, analogs with mixed opioid receptor profile gained a lot of interest. However, recently the concept of biased agonism, that highlights the fact that some ligands are able to differentially activate receptor downstream pathways, became a new approach in the design of novel drug candidates for clinical application. In this review, we summarize current knowledge on the development of opioid ligands of peptide and non-peptide structure, showing how much opioid pharmacology evolved in recent years.
引用
收藏
页码:1562 / 1575
页数:14
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