College of Medicine, QU Health, Qatar University, Doha, Qatar; Biomedical and Pharmaceutical Research Unit, QU Health, Qatar University, Doha, Qatar.
Cell Signal. 2021 Jul;83:109976. doi: 10.1016/j.cellsig.2021.109976. Epub 2021 Mar 10.
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.
肥胖是一种全球性的负担,也是一种慢性疾病,会对整体健康造成损害。胃泌素是一种由 28 个氨基酸组成的八肽激素,由胃的胃黏膜分泌。胃泌素通过其 G 蛋白偶联受体作用于下丘脑区域,调节摄食行为和葡萄糖稳态。最近,已经报道了几种调节胃泌素代谢作用的中枢途径。虽然这些信号通路可以被拮抗剂或激动剂抑制或激活,但它们也可以通过“偏向”反应选择性激活,从而在受体下游的不同途径中赋予不同程度的激活。在这里,我们综述了最近关于胃泌素偏向信号的发现,以及胃泌素激素及其受体的特性,这些特性与偏向信号有关。然后,我们评估了胃泌素受体偏向信号作为肥胖治疗有效药物治疗策略的可行性。