Oxytocin and vasopressin signaling in health and disease

被引:5
|
作者
Perisic, Monika [1 ,2 ]
Woolcock, Katrina [1 ]
Hering, Anke [3 ]
Mendel, Helen [3 ]
Muttenthaler, Markus [1 ,3 ]
机构
[1] Univ Vienna, Inst Biol Chem, Fac Chem, A-1090 Vienna, Austria
[2] Univ Vienna, Vienna Doctoral Sch Chem, A-1090 Vienna, Austria
[3] Univ Queensland, Inst Mol Biosci, Brisbane 4072, Australia
基金
澳大利亚研究理事会; 欧洲研究理事会;
关键词
RECEPTOR ANTAGONIST; SELECTIVE AGONISTS; BETA-ARRESTIN; PHARMACOLOGICAL CHARACTERIZATION; ARGININE-VASOPRESSIN; SOCIAL AVOIDANCE; V-1B RECEPTOR; V1B RECEPTORS; POTENT; DESIGN;
D O I
10.1016/j.tibs.2024.01.010
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
Neurohypophysial peptides are ancient and evolutionarily highly conserved neuropeptides that regulate many crucial physiological functions in vertebrates and invertebrates. The human neurohypophysial oxytocin/vasopressin (OT/VP) signaling system with its four receptors has become an attractive drug target for a variety of diseases, including cancer, pain, cardiovascular indications, and neurological disorders. Despite its promise, drug development faces hurdles, including signaling complexity, selectivity and off -target concerns, translational interspecies differences, and inefficient drug delivery. In this review we dive into the complexity of the OT/VP signaling system in health and disease, provide an overview of relevant pharmacological probes, and discuss the latest trends in therapeutic lead discovery and drug development.
引用
收藏
页码:361 / 377
页数:17
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