Tytgat Institute for Liver and Intestinal Research, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands.
Department of Medicine, Division of Endocrinology, and Einthoven Laboratory for Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, Netherlands.
JCI Insight. 2019 Jun 25;5(14):127197. doi: 10.1172/jci.insight.127197.
Bile acids play a major role in the regulation of lipid and energy metabolism. Here we propose the hepatic bile acid uptake transporter Na+ taurocholate co-transporting polypeptide (NTCP) as a target to prolong postprandial bile acid elevations in plasma. Reducing hepatic clearance of bile acids from plasma by genetic deletion of NTCP moderately increased plasma bile acid levels, reduced diet-induced obesity, attenuated hepatic steatosis, and lowered plasma cholesterol levels. NTCP-G protein-coupled bile acid receptor (TGR5) double knockout mice were equally protected against diet-induced-obesity as NTCP single knockout mice. NTCP knockout mice displayed decreased intestinal fat absorption and a trend towards higher fecal energy output. Furthermore, NTCP deficiency was associated with an increased uncoupled respiration in brown adipose tissue, leading to increased energy expenditure. We conclude that targeting NTCP-mediated bile acid uptake can be a novel approach to treat obesity and obesity-related hepatosteatosis by simultaneously dampening intestinal fat absorption and increasing energy expenditure.
胆汁酸在脂质和能量代谢的调节中起主要作用。在这里,我们提出将肝胆汁酸摄取转运蛋白 Na+ 牛磺胆酸钠共转运蛋白(NTCP)作为一个靶点,以延长餐后血浆胆汁酸的升高。通过基因敲除 NTCP 减少肝脏从血浆中清除胆汁酸,可适度增加血浆胆汁酸水平,减少饮食诱导的肥胖,减轻肝脂肪变性,并降低血浆胆固醇水平。NTCP-G 蛋白偶联胆汁酸受体(TGR5)双重敲除小鼠与 NTCP 单敲除小鼠一样能抵抗饮食诱导的肥胖。NTCP 敲除小鼠表现出较低的肠道脂肪吸收和粪便能量输出的趋势。此外,NTCP 缺乏与棕色脂肪组织中解偶联呼吸增加有关,导致能量消耗增加。我们得出结论,靶向 NTCP 介导的胆汁酸摄取可能是一种通过同时抑制肠道脂肪吸收和增加能量消耗来治疗肥胖和肥胖相关肝脂肪变性的新方法。