Biased signaling: A viable strategy to drug ghrelin receptors for the treatment of obesity

被引:4
|
作者
Nagi, Karim [1 ,2 ]
Habib, Abdella M. [1 ,2 ]
机构
[1] Qatar Univ, Coll Med, QU Hlth, Doha, Qatar
[2] Qatar Univ, Biomed & Pharmaceut Res Unit, QU Hlth, Doha, Qatar
关键词
Bias; Ghrelin; Biased agonism; Obesity; Dimer; Functional selectivity; HORMONE SECRETAGOGUE RECEPTOR; FOOD-INTAKE; G-PROTEIN; CONSTITUTIVE ACTIVITY; ACYLATED PEPTIDE; MESSENGER-RNA; IN-VIVO; NEURONS; IDENTIFICATION; MECHANISM;
D O I
10.1016/j.cellsig.2021.109976
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Obesity is a global burden and a chronic ailment with damaging overall health effects. Ghrelin, an octanoylated 28 amino acid peptide hormone, is secreted from the oxyntic mucosa of the stomach. Ghrelin acts on regions of the hypothalamus to regulate feeding behavior and glucose homeostasis through its G protein-coupled receptor. Recently, several central pathways modulating the metabolic actions of ghrelin have been reported. While these signaling pathways can be inhibited or activated by antagonists or agonists, they can also be discriminatingly activated in a ?biased? response to impart different degrees of activation in distinct pathways downstream of the receptor. Here, we review recent ghrelin biased signaling findings as well as characteristics of ghrelin hormone and its receptors pertinent for biased signaling. We then evaluate the feasibility for ghrelin receptor biased signaling as a strategy for the development of effective pharmacotherapy in obesity treatment.
引用
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页数:10
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