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肾脏碳水化合物代谢的代谢适应性。V. 大鼠肾小管糖异生对不同利尿剂的体内反应。

Metabolic adaptation of renal carbohydrate metabolism. V. In vivo response of rat renal-tubule gluconeogenesis to different diuretics.

作者信息

Amores M V, Hortelano P, García-Salguero L, Lupiáñez J A

机构信息

Department of Biochemistry and Molecular Biology, University of Granada, Spain.

出版信息

Mol Cell Biochem. 1994 Aug 31;137(2):117-25. doi: 10.1007/BF00944073.

Abstract

We have studied the effects of the diuretics mersalyl, furosemide and ethacrynic acid on renal gluconeogenesis is isolated rat-kidney tubules and on the activities of the most important gluconeogenic and glycolytic enzymes in both fed and fasted rats. Mersalyl (15 mg.kg-1 animal weight) significantly decreased the rate of gluconeogenesis in well-fed rats (68%) as well as in 24 and 48-h fasted ones (33 and 37% respectively). This inhibition occurred when lactate, pyruvate, glycerol or fructose were used as substrates. Ethacrynic acid at a dose of 50 mg.kg-1 animal weight provoked a transient inhibition of renal glucose production by almost 20% but only in fed rats with lactate as substrate, whereas the same dose of furosemide did not affect this metabolic pathway. Parallel to these changes, mersalyl caused a significant inhibition in the maximum activity of the most important gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, fructose 1,6-bisphosphatase and glucose 6-phosphatase, in both fed and fasted rats. Neither ethacrynic acid nor furosemide produced any variations in the activities of these enzymes. The activity of the glycolytic enzymes phosphofructokinase and pyruvate kinase was not modified by these diuretics. Nevertheless, the activity of the thiol-enzyme glyceraldehyde 3-phosphate dehydrogenase was severely inhibited by mersalyl and to a lesser extent by the other diuretics. This inhibition was higher in fasted than fed rats. Hence, we conclude that the inhibitory effect of mersalyl on renal gluconeogenesis is due, at least partly, to a decrease in the flux through the gluconeogenic enzymes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了利尿药汞撒利、呋塞米和依他尼酸对离体大鼠肾小管肾糖异生的影响,以及对进食和禁食大鼠体内最重要的糖异生和糖酵解酶活性的影响。汞撒利(15毫克/千克动物体重)显著降低了进食良好大鼠的糖异生速率(68%),以及禁食24小时和48小时大鼠的糖异生速率(分别为33%和37%)。当使用乳酸、丙酮酸、甘油或果糖作为底物时,会出现这种抑制作用。依他尼酸剂量为50毫克/千克动物体重时,仅在以乳酸为底物的进食大鼠中,短暂抑制肾葡萄糖生成近20%,而相同剂量的呋塞米对该代谢途径无影响。与这些变化同时,汞撒利在进食和禁食大鼠中均显著抑制了最重要的糖异生酶磷酸烯醇式丙酮酸羧激酶、果糖1,6 - 二磷酸酶和葡萄糖6 - 磷酸酶的最大活性。依他尼酸和呋塞米均未使这些酶的活性发生任何变化。糖酵解酶磷酸果糖激酶和丙酮酸激酶的活性未被这些利尿剂改变。然而,硫醇酶甘油醛3 - 磷酸脱氢酶的活性被汞撒利严重抑制,被其他利尿剂的抑制程度较小。这种抑制在禁食大鼠中比进食大鼠中更高。因此,我们得出结论,汞撒利对肾糖异生的抑制作用至少部分是由于糖异生酶通量的降低。(摘要截断于250字)

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