首页> 美国卫生研究院文献>Biochemical Journal >Induction and suppression of the key enzymes of glycolysis and gluconeogenesis in isolated perfused rat liver in response to glucose fructose and lactate
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Induction and suppression of the key enzymes of glycolysis and gluconeogenesis in isolated perfused rat liver in response to glucose fructose and lactate

机译:葡萄糖果糖和乳酸对离体灌注大鼠肝脏糖酵解和糖异生的关键酶的诱导和抑制

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摘要

1. Measurements were made of the activities of the four key enzymes involved in gluconeogenesis, pyruvate carboxylase (EC 6.4.1.1), phosphoenolpyruvate carboxylase (EC 4.1.1.32), fructose 1,6-diphosphatase (EC 3.1.3.11) and glucose 6-phosphatase (EC 3.1.3.9), of serine dehydratase (EC 4.2.1.13) and of the four enzymes unique to glycolysis, glucokinase (EC 2.7.1.2), hexokinase (EC 2.7.1.1), phosphofructokinase (EC 2.7.1.11) and pyruvate kinase (EC 2.7.1.40), in livers from starved rats perfused with glucose, fructose or lactate. Changes in perfusate concentrations of glucose, fructose, lactate, pyruvate, urea and amino acid were monitored for each perfusion. 2. Addition of 15mm-glucose at the start of perfusion decreased the activity of pyruvate carboxylase. Constant infusion of glucose to maintain the concentration also decreased the activities of phosphoenolpyruvate carboxylase, fructose 1,6-diphosphatase and serine dehydratase. Addition of 2.2mm-glucose initially to give a perfusate sugar concentration similar to the blood sugar concentration of starved animals had no effect on the activities of the enzymes compared with zero-time controls. 3. Addition of 15mm-fructose initially decreased glucokinase activity. Constant infusion of fructose decreased activities of glucokinase, phosphofructokinase, pyruvate carboxylase, phosphoenolpyruvate carboxylase, glucose 6-phosphatase and serine dehydratase. 4. Addition of 7mm-lactate initially elevated the activity of pyruvate carboxylase, as also did constant infusion; maintenance of a perfusate lactate concentration of 18mm induced both pyruvate carboxylase and phosphoenolpyruvate carboxylase activities. 5. Addition of cycloheximide had no effect on the activities of the enzymes after 4h of perfusion at either low or high concentrations of glucose or at high lactate concentration. Cycloheximide also prevented the loss or induction of pyruvate carboxylase and phosphoenolpyruvate carboxylase activities with high substrate concentrations. 6. Significant amounts of glycogen were deposited in all perfusions, except for those containing cycloheximide at the lowest glucose concentration. Lipid was found to increase only in the experiments with high fructose concentrations. 7. Perfusion with either fructose or glucose decreased the rates of ureogenesis; addition of cycloheximide increased urea efflux from the liver.
机译:1.测量涉及糖异生的四种关键酶,丙酮酸羧化酶(EC 6.4.1.1),磷酸烯醇丙酮酸羧化酶(EC 4.1.1.32),果糖1,6-二磷酸酶(EC 3.1.3.11)和葡萄糖6的活性。 -磷酸酶(EC 3.1.3.9),丝氨酸脱水酶(EC 4.2.1.13)和糖酵解特有的四种酶,葡萄糖激酶(EC 2.7.1.2),己糖激酶(EC 2.7.1.1),磷酸果糖激酶(EC 2.7.1.11)和饥饿的大鼠肝脏中灌注葡萄糖,果糖或乳酸盐的丙酮酸和丙酮酸激酶(EC 2.7.1.40)。每次灌注监测葡萄糖,果糖,乳酸,丙酮酸,尿素和氨基酸的灌注液浓度的变化。 2.在灌注开始时添加15mm葡萄糖会降低丙酮酸羧化酶的活性。不断输注葡萄糖以保持浓度也降低了磷酸烯醇丙酮酸羧化酶,果糖1,6-二磷酸酶和丝氨酸脱水酶的活性。与零时对照相比,最初添加2.2mm葡萄糖可得到与饥饿动物血糖浓度相似的灌注液糖浓度,对酶的活性没有影响。 3.添加15mm果糖起初降低了葡萄糖激酶活性。不断注入果糖会降低葡萄糖激酶,磷酸果糖激酶,丙酮酸羧化酶,磷酸烯醇丙酮酸羧化酶,葡萄糖6-磷酸酶和丝氨酸脱水酶的活性。 4.加入7mm-乳酸起初增加了丙酮酸羧化酶的活性,也不断地进行了输注。维持灌洗液乳酸浓度为18mm时,会引起丙酮酸羧化酶和磷酸烯醇丙酮酸羧化酶的活性。 5.在低或高浓度葡萄糖或高乳酸浓度下,灌注4h后添加环己酰亚胺对酶的活性没有影响。环己二酰亚胺还可以在高底物浓度下防止丙酮酸羧化酶和磷酸烯醇丙酮酸羧化酶活性的丧失或诱导。 6.除了含有最低浓度的环己酰亚胺的那些糖以外,所有灌注中均沉积了大量的糖原。仅在高果糖浓度的实验中发现脂质增加。 7.用果糖或葡萄糖灌注会降低尿毒症的发生率;环己酰亚胺的加入增加了尿素从肝脏的流出。

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