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Lipolytic actions of secretin in mouse adipocytes

机译:促胰液素在小鼠脂肪细胞中的脂解作用

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摘要

Secretin (Sct), a classical gut hormone, is now known to play pleiotropic functions in the body including osmoregulation, digestion, and feeding control. As Sct has long been implicated to regulate metabolism, in this report, we have investigated a potential lipolytic action of Sct. In our preliminary studies, both Sct levels in circulation and Sct receptor (SctR) transcripts in adipose tissue were upregulated during fasting, suggesting a potential physiological relevance of Sct in regulating lipolysis. Using SctR knockout and Sct knockout mice as controls, we show that Sct is able to stimulate lipolysis in vitro in isolated adipocytes dose- and time-dependently, as well as acute lipolysis in vivo. H-89, a protein kinase A (PKA) inhibitor, was found to attenuate lipolytic effects of 1 μM Sct in vitro, while a significant increase in PKA activity upon Sct injection was observed in the adipose tissue in vivo. Sct was also found to stimulate phosphorylation at 660ser of hormone sensitive lipase (HSL) and to bring about the translocation of HSL from cytosol to the lipid droplet. In summary, our data demonstrate for the first time the in vivo and in vitro lipolytic effects of Sct, and that this function is mediated by PKA and HSL.
机译:分泌素(Sctin)是一种经典的肠道激素,目前已知在人体内发挥多效性功能,包括渗透调节,消化和喂养控制。由于Sct长期参与调节新陈代谢,因此在本报告中,我们研究了Sct的潜在脂解作用。在我们的初步研究中,禁食期间,循环中的Sct水平和脂肪组织中的Sct受体(SctR)转录本均被上调,表明Sct在调节脂解中具有潜在的生理意义。使用SctR基因敲除小鼠和Sct基因敲除小鼠作为对照,我们表明Sct能够在体外在离体的脂肪细胞中以剂量和时间依赖性方式刺激脂解,以及在体内进行急性脂解。发现H-89是一种蛋白激酶A(PKA)抑制剂,在体外可减弱1μMSct的脂解作用,而在体内脂肪组织中观察到Sct注射后PKA活性显着增加。还发现了Sct可以刺激激素敏感性脂肪酶(HSL)在660 sser处磷酸化,并导致HSL从胞质溶胶向脂质滴转移。总而言之,我们的数据首次证明了Sct的体内和体外脂解作用,并且该功能是由PKA和HSL介导的。

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