医学
代谢综合征
可药性
胰岛素抵抗
背景(考古学)
肥胖
疾病
干预(咨询)
心理干预
生物信息学
糖尿病
重症监护医学
内科学
内分泌学
基因
精神科
生物
古生物学
生物化学
化学
作者
Michael Fragner,Manish A. Parikh,Kaedrea A. Jackson,Michal L. Schwartzman,William H. Frishman,Stephen J. Peterson
标识
DOI:10.1097/crd.0000000000000711
摘要
Metabolic syndrome increases the risk of stroke, cardiovascular disease, and diabetes. The morbidity and mortality associated with this constellation of risk factors are equally alarming when considering the economic and global significance that this epidemic has on an institutional and patient level. Despite several current treatments available, there needs to be a continuous effort to explore more specific and effective druggable entities for preventative and therapeutic interventions. Within this context, the G-protein coupled receptor, GPR75, is an attractive pharmacological target. GPR75 and its association with its ligand, 20-hydroxyeicosatetraenoic acid, have been shown to promote hypertension, inflammation, obesity, and insulin resistance. This review will help shed light on this novel signaling pathway and offer a perspective on a promising new direction of targeting different aspects of the metabolic syndrome involving GPR75. Gene targeting of GPR75 is more effective than current pharmacologic therapies without the known side effects.
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