TY - JOUR
T1 - Biased ligands at opioid receptors
T2 - Current status and future directions
AU - Che, Tao
AU - Dwivedi-Agnihotri, Hemlata
AU - Shukla, Arun K.
AU - Roth, Bryan L.
N1 - Publisher Copyright:
© 2021 American Association for the Advancement of Science. All rights reserved.
PY - 2021/4/6
Y1 - 2021/4/6
N2 - The opioid crisis represents a major worldwide public health crisis that has accelerated the search for safer and more effective opioids. Over the past few years, the identification of biased opioid ligands capable of eliciting selective functional responses has provided an alternative avenue to develop novel therapeutics without the side effects of current opioid medications. However, whether biased agonism or other pharmacological properties, such as partial agonism (or low efficacy), account for the therapeutic benefits remains questionable. Here, we provide a summary of the current status of biased opioid ligands that target the-and-opioid receptors and highlight advances in preclinical and clinical trials of some of these ligands. We also discuss an example of structure-based biased ligand discovery at the-opioid receptor, an approach that could revolutionize drug discovery at opioid and other receptors. Last, we briefly discuss caveats and future directions for this important area of research.
AB - The opioid crisis represents a major worldwide public health crisis that has accelerated the search for safer and more effective opioids. Over the past few years, the identification of biased opioid ligands capable of eliciting selective functional responses has provided an alternative avenue to develop novel therapeutics without the side effects of current opioid medications. However, whether biased agonism or other pharmacological properties, such as partial agonism (or low efficacy), account for the therapeutic benefits remains questionable. Here, we provide a summary of the current status of biased opioid ligands that target the-and-opioid receptors and highlight advances in preclinical and clinical trials of some of these ligands. We also discuss an example of structure-based biased ligand discovery at the-opioid receptor, an approach that could revolutionize drug discovery at opioid and other receptors. Last, we briefly discuss caveats and future directions for this important area of research.
UR - http://www.scopus.com/inward/record.url?scp=85103998220&partnerID=8YFLogxK
U2 - 10.1126/scisignal.aav0320
DO - 10.1126/scisignal.aav0320
M3 - Review article
C2 - 33824179
AN - SCOPUS:85103998220
SN - 1945-0877
VL - 14
JO - Science signaling
JF - Science signaling
IS - 677
M1 - eaav0320
ER -