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肝细胞中ATP和无机磷酸盐耗竭诱导的磷酸核糖焦磷酸增加。

Increase in phosphoribosyl pyrophosphate induced by ATP and Pi depletion in hepatocytes.

作者信息

Vincent M F, Van den Berghe G, Hers H G

机构信息

Laboratory of Physiological Chemistry, International Institute of Cellular and Molecular Pathology, Brussels, Belgium.

出版信息

FASEB J. 1989 May;3(7):1862-7. doi: 10.1096/fasebj.3.7.2469615.

Abstract

A series of compounds that induce depletion of ATP and Pi when added to isolated rat hepatocytes were found to cause a remarkable, although transient, elevation in the concentration of phosphoribosyl pyrophosphate (PRPP) in these cells. After the addition of 5 mM fructose, xylitol, tagatose, or D-xylulose, PRPP increased from a basal value of 6 +/- 1 nmol/g of cells to, respectively, 68 +/- 11, 42 +/- 11, 67 +/- 22, and 530 +/- 50 nmol/g of cells (means +/- SEM of 3-9 experiments). In each case, the increase in PRPP was preceded by a latency period of 5-10 min. PRPP reached maximal levels 15 min after the addition of fructose and 30 min after that of xylitol and D-xylulose, but continued to increase for as long as 60 min after the addition of tagatose. Most striking was that the increase in PRPP closely paralleled the restoration of intracellular Pi. Ribose 5-P increased about two- to fivefold after the addition of fructose, xylitol, and tagatose, and approximately 12-fold after D-xylulose. The mechanism by which ATP- and Pi-depleting compounds stimulate the activity of PRPP synthetase in isolated rat hepatocytes is discussed.

摘要

当向分离的大鼠肝细胞中添加一系列能诱导ATP和无机磷酸(Pi)消耗的化合物时,发现这些细胞中的磷酸核糖焦磷酸(PRPP)浓度会显著升高,尽管这种升高是短暂的。添加5 mM果糖、木糖醇、塔格糖或D-木酮糖后,PRPP分别从6±1 nmol/g细胞的基础值升高到68±11、42±11、67±22和530±50 nmol/g细胞(3至9次实验的平均值±标准误)。在每种情况下,PRPP升高之前都有5至10分钟的潜伏期。添加果糖后15分钟、木糖醇和D-木酮糖后30分钟,PRPP达到最高水平,但添加塔格糖后60分钟内PRPP仍持续升高。最引人注目的是,PRPP的升高与细胞内Pi的恢复密切平行。添加果糖、木糖醇和塔格糖后,5-磷酸核糖增加约2至5倍,添加D-木酮糖后增加约12倍。本文讨论了消耗ATP和Pi的化合物刺激分离的大鼠肝细胞中PRPP合成酶活性的机制。

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