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酮糖在分离的肝细胞中诱导呼吸抑制。

Ketose induced respiratory inhibition in isolated hepatocytes.

作者信息

Martínez P, Carrascosa J M, Núñez de Castro I

机构信息

Departamento de Bioquímica, Facultad de Ciencias, Málaga, Spain.

出版信息

Rev Esp Fisiol. 1987 Jun;43(2):163-71.

PMID:3659542
Abstract

The addition of 10 mM fructose or 10 mM tagatose to a suspension of hepatocytes caused respiratory inhibition, whereas no change in oxygen uptake was observed following the addition of glucose. However, incubations in the presence of fructose showed a high, aerobic glycolytic activity. Tagatose is phosphorylated to tagatose 1-phosphate but is not further metabolized by cell free liver extract. Moreover, the addition of fructose to glucagon treated cells also caused the Crabtree-like effect. The concentration of adenine nucleotides and inorganic phosphate (Pi) in the mitochondrial and cytosolic compartments during incubation (time 30 min) was determined by the digitonin fractionation procedure. In the presence of 10 mM fructose or tagatose, the total adenine nucleotide pools decreased by 40%; however, glucose produced no change. The addition of ketoses diminished the asymmetric distribution of extramitochondrial (ATP/ADP)e ratio and intramitochondrial (ATP/ADP)i ratio. At the same time the total mitochondrial Pi fell from 17 mM to 6-7 mM. The mitochondrial membrane potential (-161 mV) in the presence of fructose showed no changes during the 30 min experimental period. An increase in the NADH/NAD+ ratio was observed. These results suggest that in hepatocytes the inhibition of respiration is not necessarily linked with the enhanced aerobic glycolysis, by competition for common substrates.

摘要

向肝细胞悬液中添加10 mM果糖或10 mM塔格糖会导致呼吸抑制,而添加葡萄糖后未观察到氧摄取的变化。然而,在果糖存在下孵育显示出高需氧糖酵解活性。塔格糖磷酸化为1-磷酸塔格糖,但不能被无细胞肝提取物进一步代谢。此外,向用胰高血糖素处理的细胞中添加果糖也会引起类似克氏效应。通过洋地黄皂苷分级分离法测定孵育期间(30分钟)线粒体和细胞溶质区室中腺嘌呤核苷酸和无机磷酸盐(Pi)的浓度。在10 mM果糖或塔格糖存在下,总腺嘌呤核苷酸池减少了40%;然而,葡萄糖没有产生变化。添加酮糖减少了线粒体外(ATP/ADP)e比值和线粒体内(ATP/ADP)i比值的不对称分布。同时,线粒体总Pi从17 mM降至6 - 7 mM。在果糖存在下,线粒体膜电位(-161 mV)在30分钟实验期间没有变化。观察到NADH/NAD +比值增加。这些结果表明,在肝细胞中,呼吸抑制不一定与因竞争共同底物而增强的需氧糖酵解相关。

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