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[红细胞中糖酵解途径与磷酸己糖旁路的相互作用]

[Interaction of the Embden-Meyerhof pathway and hexose monophosphate shunt in erythrocytes].

作者信息

Ataullakhanov F I, Buravtsev V N, Zhabotinskiĩ A M, Norina S B, Pichugin A V

出版信息

Biokhimiia. 1981 Apr;46(4):723-31.

PMID:7284486
Abstract

A mathematical model of glycolysis in human erythrocytes for the interaction between the Embden-Meyerhof and the pentose phosphate pathways has been developed. The characteristic surfaces, i. e. interdependencies between the rates of metabolite flows in both pathways and ATP and NADPH concentrations have been calculated. The model obtained is well correlated with the experimental data on glycolysis characteristic at low rates of the pentose phosphate pathway reactions. The model suggests that NADPH and GSH concentrations should be stabilized. At ATP and NADPH concentrations close to the physiological ones the Embden-Meyerhof and pentose phosphate pathways function practically independently. When the NADPH concentration is decreased below 80% of the physiological value, the system ceases to stabilize the ATP concentration. In its turn, a decrease of ATP concentration results in a corresponding decrease of the maximal rate of the pentose phosphate pathway.

摘要

已建立了一个关于人类红细胞糖酵解的数学模型,用于描述糖酵解途径(Embden-Meyerhof途径)和磷酸戊糖途径之间的相互作用。计算了特征表面,即两条途径中代谢物流速与ATP和NADPH浓度之间的相互依存关系。所得到的模型与磷酸戊糖途径反应低速率下糖酵解特征的实验数据具有良好的相关性。该模型表明NADPH和谷胱甘肽(GSH)浓度应保持稳定。当ATP和NADPH浓度接近生理浓度时,糖酵解途径和磷酸戊糖途径实际上是独立发挥作用的。当NADPH浓度降至生理值的80%以下时,该系统便不再能稳定ATP浓度。反过来,ATP浓度的降低会导致磷酸戊糖途径最大速率相应下降。

相似文献

1
[Interaction of the Embden-Meyerhof pathway and hexose monophosphate shunt in erythrocytes].[红细胞中糖酵解途径与磷酸己糖旁路的相互作用]
Biokhimiia. 1981 Apr;46(4):723-31.
2
[Dependence of effectiveness of the pentose pathway on ATP concentration in erythrocytes].[红细胞中戊糖途径的有效性对ATP浓度的依赖性]
Biokhimiia. 1981 Apr;46(4):758-60.
3
NADPH production in the oxidative pentose phosphate pathway as source of reducing equivalents in glycolysis of human red cells in vitro.体外人红细胞糖酵解中作为还原当量来源的氧化戊糖磷酸途径中的NADPH生成
Acta Biol Med Ger. 1979;38(7):901-8.
4
[Pentose monophoshate pathway and the glutathione system in physiological pregnancy].[生理妊娠中的磷酸戊糖途径与谷胱甘肽系统]
Vopr Med Khim. 1985 Mar-Apr;31(2):33-6.
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[Mathematical model for energy metabolism in erythrocytes. Independence of scaled glycolytic characteristics of individual features of the donors].[红细胞能量代谢的数学模型。供体个体特征对糖酵解特征缩放的独立性]
Biokhimiia. 1980 Jul;45(7):1267-73.
6
[Quantitative model of human erythrocyte glycolysis. I. Relationship between the stationary rate of glycolysis and the ATP concentration].[人类红细胞糖酵解的定量模型。I. 糖酵解的稳定速率与ATP浓度之间的关系]
Biofizika. 1977 May-Jun;22(3):483-8.
7
[Regulatory characteristics of the metabolic systems and the stabilization of the relative concentrations of ATP and reduced glutathione in human erythrocytes].[人体红细胞代谢系统的调节特性以及三磷酸腺苷和还原型谷胱甘肽相对浓度的稳定]
Izv Akad Nauk SSSR Biol. 1982 May-Jun(3):406-18.
8
Redox metabolism of glutathione in the red blood cell.红细胞中谷胱甘肽的氧化还原代谢
Acta Biol Med Ger. 1975;34(2):203-28.
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Red cell metabolism in high and low glutathione goats.高谷胱甘肽和低谷胱甘肽山羊的红细胞代谢
Enzyme. 1976;21(3):243-7. doi: 10.1159/000458864.
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[Dependence of the rate of the pentose cycle reactions on the degree of glutathione reduction in erythrocytes].[戊糖循环反应速率对红细胞中谷胱甘肽还原程度的依赖性]
Biokhimiia. 1981 Mar;46(3):530-41.

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