首页> 美国卫生研究院文献>Biochemical Journal >Fructose-induced increase in intracellular free Mg2+ ion concentration in rat hepatocytes: relation with the enzymes of glycogen metabolism.
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Fructose-induced increase in intracellular free Mg2+ ion concentration in rat hepatocytes: relation with the enzymes of glycogen metabolism.

机译:果糖诱导的大鼠肝细胞内细胞内游离Mg2 +离子浓度增加:与糖原代谢酶的关系。

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摘要

In rat hepatocytes subjected to a fructose load, ATP content decreased from 3.8 to 2.6 micromol/g of cells. Under these conditions, the intracellular free Mg2+ ion concentration,as measured with mag-fura 2, increased from 0.25 to 0.43 micromol/g of cells and 0.35 micromol of Mg2+ ions were released per g of cells in the extracellular medium. Therefore the increase in the intracellular free Mg2+ ion concentration was less than expected from the decrease in ATP, indicating that approx. 80% of the Mg2+ ions released from MgATP2- were buffered inside the cells. When this buffer capacity was challenged with an extra Mg2+ ion load by blocking the fructose-induced Mg2+ efflux, again approx. 80% of the extra Mg2+ ion load was buffered. The remaining 20% appearing as free Mg2+ions in fructose-treated hepatocytes could act as second messenger for enzymes having a Km for Mg2+ in the millimolar range. Fructose activated glycogen synthase and glycogen phosphorylase, although both the time course and the dose-dependence of activation were different. This was reflected in a stimulation of glycogen synthesis with concentrations of fructose below 5 mM. Indeed, activation of glycogen synthase reached a maximum at 30 min of incubation and was observed with small (5 mM or less) concentrations of fructose, whereas the activation of glycogen phosphorylase was almost immediate (within 5 min) and maximal with large doses of fructose. The fructose-induced activation of glycogen phosphorylase, but not that of glycogen synthase, could be related to an increase in free Mg2+ ion concentration.
机译:在果糖负荷下的大鼠肝细胞中,ATP含量从3.8微摩尔/克降至2.6微摩尔/克。在这些条件下,用磁熔法2测定的细胞内游离Mg2 +离子浓度从0.25增加到0.43微摩尔/克细胞,每克细胞在细胞外培养基中释放出0.35微摩尔Mg2 +离子。因此,细胞内游离Mg2 +离子浓度的增加小于ATP减少所预期的浓度,表明从MgATP2-释放的Mg2 +离子中有80%缓冲在细胞内。当通过阻止果糖诱导的Mg2 +流出时,该缓冲容量受到额外的Mg2 +离子负荷的挑战时,再次达到缓冲了80%的额外Mg2 +离子负载。在果糖处理的肝细胞中以游离Mg2 +离子形式出现的其余20%可以充当Mg2 +的Km在毫摩尔范围内的酶的第二信使。果糖激活的糖原合酶和糖原磷酸化酶,尽管激活的时间过程和剂量依赖性不同。这反映在果糖浓度低于5 mM时对糖原合成的刺激。实际上,在孵育30分钟时,糖原合酶的激活达到最大值,并且在低浓度(5 mM或更少)的果糖中观察到,而糖原磷酸化酶的激活几乎立即(在5分钟内),而在大剂量果糖时则达到最大。 。果糖诱导的糖原磷酸化酶的活化,而不是糖原合酶的活化,可能与游离Mg2 +离子浓度的增加有关。

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