Net glucose production from acetone in isolated murine hepatocytes. The effect of different pretreatments of mice

Miklós Péter Kalapos, József Mandl, Gábor Bánhegyi, Ferenc Antoni , Tamás Garzó
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引用次数: 15

Abstract

  • 1.

    1. To evaluate the condition under which net glucose production from acetone, added as sole substrate, occurs different pretreatments of mice, in combination with starvation, were used; (i) acetone pretreatment (acetone is a known inducer of cytochrome P-450 isozymes involved in this pathway), (ii) fructose pretreatment (to induce NADPH + H+ generating enzymes) or (iii) their combination.

  • 2.

    2. There was net glucose formation from acetone only in that case, when the cells were prepared from 48 hr fasted animals pretreated with both acetone and fructose. However, using 2-14C-acetone, incorporation of 14C-carbon into glucose could be detected in all the cases and, at the same time, acetone was without any effect on protein synthesis.

  • 3.

    3. The addition of acetone increased gluconeogenesis from alanine in almost all the cases. The only exception from this general rule was that the case, when hepatocytes were prepared from acetone pretreated 48 hr starved mice where, instead of the elevation of glucose formation, a decrease of that was caused by acetone.

  • 4.

    4. Acetone decreased 14C-carbon incorporation into glucose from 14C-(U)-alanine added at saturating concentration in hepatocytes prepared from starved mice.

  • 5.

    5. Similarly to acetone there was no net glucose formation from acetol either when added alone, however, it enhanced gluconeogenesis from alanine at non-saturating concentrations of the amino acid.

  • 6.

    6. Methylglyoxal proved gluconeogenic in all the cases.

  • 7.

    7. It is concluded that net glucose formation from acetone as sole substrate occurs only under those conditions which are far from a physiological situation, however, when gluconeogenesis from another substrate takes place, acetone can contribute to net glucose formation in hepatocytes prepared from fasted mice.

丙酮在小鼠肝细胞中的净葡萄糖产量。不同预处理对小鼠的影响
1.1. 研究了以丙酮为底物的小鼠在不同预处理条件下的净葡萄糖产率。(i)丙酮预处理(丙酮是参与该途径的细胞色素P-450同工酶的已知诱导剂),(ii)果糖预处理(诱导NADPH + H+生成酶)或(iii)它们的组合。只有在这种情况下,当用丙酮和果糖预处理48小时的禁食动物制备细胞时,丙酮才会产生净葡萄糖。然而,使用2- 14c -丙酮,在所有情况下都可以检测到14c -碳掺入葡萄糖,同时,丙酮对蛋白质合成没有任何影响。在几乎所有的情况下,丙酮的加入增加了丙氨酸的糖异生。这一普遍规律的唯一例外是,当用丙酮预处理48小时的饥饿小鼠制备肝细胞时,丙酮非但没有增加葡萄糖的形成,反而减少了葡萄糖的形成。在饥饿小鼠制备的肝细胞中,以饱和浓度添加的14C-(U)-丙氨酸减少了14C-碳向葡萄糖的掺入。与丙酮类似,单独加入乙酰醇也不会产生净葡萄糖,但是,在氨基酸浓度不饱和的情况下,乙酰醇能促进丙氨酸的糖异生。甲基乙二醛在所有病例中均被证实为糖异生。综上所述,丙酮作为唯一底物仅在远离生理状况的条件下形成净葡萄糖,然而,当其他底物发生糖异生时,丙酮可以促进空腹小鼠肝细胞的净葡萄糖形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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