Patented TGR5 modulators: a review (2006-present)

被引:47
作者
Gioiello, Antimo [1 ]
Rosatelli, Emiliano [1 ]
Nuti, Roberto [1 ,2 ]
Macchiarulo, Antonio [1 ]
Pellicciari, Roberto [1 ,2 ]
机构
[1] Univ Perugia, Dipartimento Chim & Tecnol Farmaco, I-06123 Perugia, Italy
[2] TES Pharma Srl, I-306073 Perugia, Italy
关键词
atherosclerosis; bile acid; diabesity; glucagon-like peptide-1; G-protein coupled receptor; liver disease; metabolic syndrome; structure-activity relationships; TGR5; BILE-ACID RECEPTOR; NF-KAPPA-B; NUCLEAR RECEPTOR; GPBAR1; TGR5; ACTIVATION; INFLAMMATION; DERIVATIVES; POTENT; IDENTIFICATION; EXPRESSION;
D O I
10.1517/13543776.2012.733000
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: The G protein-coupled receptor TGR5 is a key player of the bile acid signaling network, and its activation has been proved to increase the glycemic control, to enhance energy expenditure and to exert anti-inflammatory actions. Accordingly, TGR5 ligands have emerged in drug discovery and preclinical appraisals as promising agents for the treatment of liver diseases, metabolic syndrome and related disorders. Areas covered: Recent advances in the field of TGR5 modulators are reviewed, with a particular attention on patent applications and peer-reviewed publications in the past 6 years. Expert opinion: Activation of TGR5 showed to protect mice from diabesity and insulin resistance, to improve liver functions, as well as to attenuate the development of atherosclerosis. However, although the efficacy of TGR5 agonists in mice is encouraging, further studies are needed to determine their potential in humans and to evaluate carefully the balance between the therapeutic benefits and adverse effects associated with the target. The development of new TGR5 selective ligands to support studies in animal models will surely facilitate the understanding of the complexity of TGR5 signaling network.
引用
收藏
页码:1399 / 1414
页数:16
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