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Sphingosine-1-phosphate signaling and the gut-liver axis in liver diseases

机译:鞘氨醇-1-磷酸信号转导和肝脏疾病中的肠肝轴

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The liver is the central organ involved in lipid metabolism and the gastrointestinal (GI) tract is responsible for nutrient absorption and partitioning. Obesity, dyslipidemia and metabolic disorders are of increasing public health concern worldwide, and novel therapeutics that target both the liver and the GI tract (gut-liver axis) are much needed. In addition to aiding fat digestion, bile acids act as important signaling molecules that regulate lipid, glucose and energy metabolism via activating nuclear receptor, G protein-coupled receptors (GPCRs), Takeda G protein receptor 5 (TGR5) and sphingosine-1-phosphate receptor 2 (S1PR2). Sphingosine-1-phosphate (S1P) is synthesized by two sphingosine kinase isoforms and is a potent signaling molecule that plays a critical role in various diseases such as fatty liver, inflammatory bowel disease (IBD) and colorectal cancer. In this review, we will focus on recent findings related to the role of S1P-mediated signaling pathways in the gut-liver axis.
机译:肝脏是参与脂质代谢的中央器官,胃肠道(GI)负责营养的吸收和分配。肥胖,血脂异常和代谢紊乱在全球范围内日益引起公众关注,因此,迫切需要针对肝脏和胃肠道(肠肝轴)的新型疗法。除了帮助脂肪消化外,胆汁酸还通过激活核受体,G蛋白偶联受体(GPCR),武田G蛋白受体5(TGR5)和鞘氨醇-1-磷酸来调节脂质,葡萄糖和能量代谢,是重要的信号分子。受体2(S1PR2)。鞘氨醇-1-磷酸酯(S1P)由两种鞘氨醇激酶同工型合成,是一种有效的信号分子,在多种疾病(例如脂肪肝,炎性肠病(IBD)和结直肠癌)中起关键作用。在这篇综述中,我们将重点关注与S1P介导的信号途径在肠肝轴中的作用有关的最新发现。

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