Endogenous glucose production is inhibited by the adipose-derived protein Acrp30
Endogenous glucose production is inhibited by the adipose-derived protein Acrp30
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DOI：
10.1172/jci14120
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发表时间：
2001-12-01
影响因子：
15.9
通讯作者：
Rossetti, L
中科院分区：
文献类型：
--
作者：
Combs, TP;Berg, AH;Rossetti, L
腹腔注射纯化的重组Acrp30可降低小鼠的血糖水平。为了深入了解这种降血糖作用的机制(S)，在胰腺正常血糖钳夹期间，将纯化的重组Acrp30注入清醒的小鼠。在存在生理性高胰岛素血症的情况下，这种治疗方法使循环中的Acrp30水平增加约两倍，并刺激葡萄糖代谢。Acrp30对体内胰岛素作用的影响完全是由于葡萄糖生成率降低了65%。同样，通过葡萄糖-6-磷酸酶(G6Pase)的葡萄糖流量随着Acrp30的增加而降低，而作为肝脏葡萄糖磷酸化指标的葡萄糖-6-磷酸生物合成的直接途径的活性显著增加。Acrp30不影响葡萄糖摄取、糖酵解或糖原合成的速率。这些结果表明，循环中Acrp30水平的急剧增加降低了肝脏葡萄糖的产生，而不影响外周葡萄糖的摄取。经Acrp30输注后，肝脏糖异生酶磷酸烯醇式丙酮酸羧激酶和G6Pase mRNAs的表达较空白对照组降低了50%以上。因此，脂肪衍生蛋白Acrp30循环水平的适度上升既抑制了肝脏糖异生酶的表达，也抑制了内源性葡萄糖的产生速度。
Intraperitoneal injection of purified recombinant Acrp30 lowers glucose levels in mice. To gain insight into the mechanism(s) of this hypoglycemic effect, purified recombinant Acrp30 was infused in conscious mice during a pancreatic euglycemic clamp. In the presence of physiological hyperinsulinemia, this treatment increased circulating Acrp30 levels by approximately twofold and stimulated glucose metabolism. The effect of Acrp30 on in vivo insulin action was completely accounted for by a 65% reduction in the rate of glucose production. Similarly, glucose flux through glucose-6-phosphatase (G6Pase) decreased with Acrp30, whereas the activity of the direct pathway of glucose-6-phosphate biosynthesis, an index of hepatic glucose phosphorylation, increased significantly. Acrp30 did not affect the rates of glucose uptake, glycolysis, or glycogen synthesis. These results indicate that an acute increase in circulating Acrp30 levels lowers hepatic glucose production without affecting peripheral glucose uptake. Hepatic expression of the gluconeogenic enzymes phosphoenolpyruvate carboxykinase and G6Pase mRNAs was reduced by more than 50% following Acrp30 infusion compared with vehicle infusion. Thus, a moderate rise in circulating levels of the adipose-derived protein Acrp30 inhibits both the expression of hepatic gluconeogenic enzymes and the rate of endogenous glucose production.