FGF1 and FGF19 reverse diabetes by suppression of the hypothalamic-pituitary-adrenal axis

被引:120
作者
Perry, Rachel J. [1 ,2 ,3 ]
Lee, Sangwon [2 ,4 ]
Ma, Lie [2 ,4 ]
Zhang, Dongyan [1 ]
Schlessinger, Joseph [2 ,4 ]
Shulman, Gerald I. [1 ,2 ,3 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
HEPATIC INSULIN-RESISTANCE; METABOLIC-RATE; MICE; STEATOSIS; LOCUS;
D O I
10.1038/ncomms7980
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
zFibroblast growth factor-1 (FGF1) and FGF19 have been shown to improve glucose metabolism in diabetic rodents, but how this occurs is unknown. Here to investigate the mechanism of action of these growth factors, we perform intracerebroventricular (ICV) injections of recombinant FGF1 or FGF19 in an awake rat model of type 1 diabetes (T1D) and measure rates of whole-body lipolysis, hepatic acetyl CoA content, pyruvate carboxylase activity and hepatic glucose production. We show that ICV injection of FGF19 or FGF1 leads to similar to 60% reduction in hepatic glucose production, hepatic acetyl CoA content and whole-body lipolysis, which results from decreases in plasma ACTH and corticosterone concentrations. These effects are abrogated by an intra-arterial infusion of corticosterone. Taken together these studies identify suppression of the HPA axis and ensuing reductions in hepatic acetyl CoA content as a common mechanism responsible for mediating the acute, insulin-independent, glucose-lowering effects of FGF1 and FGF19 in rodents with poorly controlled T1D.
引用
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页数:10
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