Haut M J, London J W, Garfinkel D
Biochem J. 1974 Mar;138(3):511-24. doi: 10.1042/bj1380511.
A computer model representing the pentose cycle, the tricarboxylic acid cycle and glycolysis in slices of lactating rat mammary glands has been constructed. This model is based primarily on the studies, with radioactive chemicals, of Abraham & Chaikoff (1959) [although some of the discrepant data of Katz & Wals (1972) could be accommodated by changing one enzyme activity]. Data obtained by using [1-(14)C]-, [6-(14)C]- and [3,4-(14)C]-glucose were simulated, as well as data obtained by using unlabelled glucose (for which some new experimental data are presented). Much past work on the pentose cycle has been mainly concerned with the division of glucose flow between the pentose cycle and glycolysis, and has relied on the assumption that the system is in steady state (both labelled and unlabelled). This assumption may not apply to lactating rat mammary glands, since the model shows that the percentage flow through the shunt progressively decreased for the first 2h of a 3h experiment, and we were unable to construct a completely steady-state model. The model allows examination of many quantitative features of the system, especially the amount of material passing through key enzymes, some of which appear to be regulated by NADP(+) concentrations as proposed by McLean (1960). Supplementary information for this paper has been deposited as Supplementary Publication SUP 50023 at the British Museum (Lending Division) (formerly the National Lending Library for Science and Technology), Boston Spa, Yorks. LS23 7BQ, U.K., from whom copies can be obtained on the terms indicated in Biochem. J. (1973) 131, 5.
已构建了一个计算机模型,该模型可呈现泌乳大鼠乳腺切片中的戊糖循环、三羧酸循环和糖酵解过程。此模型主要基于亚伯拉罕和柴科夫(1959年)用放射性化学物质开展的研究[不过,卡茨和沃尔斯(1972年)的一些不一致数据可通过改变一种酶活性来解释]。模拟了使用[1-(14)C]-、[6-(14)C]-和[3,4-(14)C]-葡萄糖获得的数据,以及使用未标记葡萄糖获得的数据(文中给出了一些新的实验数据)。过去许多关于戊糖循环的研究主要关注葡萄糖在戊糖循环和糖酵解之间的流量分配,并且依赖于该系统处于稳态(标记和未标记的均是)这一假设。该假设可能不适用于泌乳大鼠乳腺,因为模型显示,在3小时实验的前2小时内,通过分流途径的流量百分比逐渐下降,而且我们无法构建一个完全稳态的模型。该模型可用于研究该系统的许多定量特征,尤其是通过关键酶的物质数量,其中一些关键酶似乎如麦克林(1960年)所提出的那样受NADP(+)浓度调节。本文的补充信息已作为补充出版物SUP 50023存放在英国约克郡波士顿温泉市LS23 7BQ的大英博物馆(出借部)(原国家科学技术出借图书馆),可按《生物化学杂志》(1973年)131卷5期所示条件从该处获取副本。