Sodium tungstate mimics insulin effect on nuclear translocation of FBPase in rat liver

R. Bertinat, F. Nualart, J. C. Slebe, A. Yáñez
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引用次数: 2

Abstract

Sodium tungstate (NaW) is an inorganic salt that has proven to be a potent insulin-mimetic agent, although the molecular events seems to differ. Inhibition of hepatic gluconeogenesis is one significant physiological action of insulin, therefore studying the effect of NaW on gluconeogenic enzymes will contribute to understand its elusive mechanism of action. Here, we show that NaW has no inhibitory effect over the gluconeogenic enzyme fructose 1,6-bisphosphatase (FBPase) in vitro, but mimics insulin in the induction of the nuclear translocation of FBPase in rat liver, which may have a negative impact on its activity. Then, at least in part, NaW may inhibit hepatic gluconeogenesis by inducing the proper subcellular distribution of FBPase, without directly interfering with its phosphatase activity.
钨酸钠模拟胰岛素对大鼠肝脏FBPase核易位的影响
钨酸钠(NaW)是一种无机盐,已被证明是一种有效的胰岛素模拟剂,尽管分子事件似乎有所不同。抑制肝脏糖异生是胰岛素的一项重要生理作用,因此研究NaW对糖异生酶的影响将有助于了解其难以理解的作用机制。在体外实验中,我们发现NaW对糖异生酶果糖1,6-二磷酸酶(FBPase)没有抑制作用,但在大鼠肝脏中模拟胰岛素诱导FBPase的核易位,这可能对其活性产生负面影响。因此,至少在一定程度上,NaW可能通过诱导FBPase的适当亚细胞分布来抑制肝脏糖异生,而不会直接干扰其磷酸酶活性。
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