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高细胞外氯化钠诱导肾髓质细胞中醛糖还原酶的信号。

Signal for induction of aldose reductase in renal medullary cells by high external NaCl.

作者信息

Uchida S, Garcia-Perez A, Murphy H, Burg M

机构信息

National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.

出版信息

Am J Physiol. 1989 Mar;256(3 Pt 1):C614-20. doi: 10.1152/ajpcell.1989.256.3.C614.

Abstract

GRB-PAP1 is a continuous line of epithelial cells derived from rabbit renal inner medulla. These cells accumulate large amounts of sorbitol when extracellular NaCl concentration is elevated. The accumulation involves an increase in aldose reductase, an enzyme that catalyzes production of sorbitol from glucose. The purpose of the present studies was to investigate the mechanism by which high NaCl triggers an increase in aldose reductase activity. When NaCl was added to increase medium osmolality from 300 to 500 mosmol/kg, enzyme activity began to increase after 12-24 h, was half-maximal in 2 days, and was maximal by 4 days. To test the effect of other solutes, medium osmolality was increased to 500 mosmol/kg by adding raffinose, urea, or glycerol. Raffinose increased aldose reductase activity as much as NaCl did. In contrast, neither urea nor glycerol affected the enzyme activity. NaCl and raffinose caused a sustained decrease in cell water content and an increase in cell sodium and potassium concentration, but urea did not. In some experiments, ouabain was added either with or without an increase in osmolality. Taking into account all of the experiments, with and without ouabain, we found that aldose reductase activity did not correlate with either cell sodium concentration or cell water content alone. It did correlate, however, with cell potassium concentration and even more strongly with the sum of cell sodium plus potassium concentration. We conclude that the signal by which hyperosmolality triggers an increase in aldose reductase activity most likely involves an increase in intracellular ionic strength.

摘要

GRB - PAP1是源自兔肾内髓的上皮细胞系。当细胞外氯化钠浓度升高时,这些细胞会积累大量山梨醇。这种积累涉及醛糖还原酶的增加,醛糖还原酶是一种催化从葡萄糖生成山梨醇的酶。本研究的目的是探讨高氯化钠引发醛糖还原酶活性增加的机制。当添加氯化钠使培养基渗透压从300 mosmol/kg增加到500 mosmol/kg时,酶活性在12 - 24小时后开始增加,2天时达到最大值的一半,4天时达到最大值。为了测试其他溶质的作用,通过添加棉子糖、尿素或甘油将培养基渗透压提高到500 mosmol/kg。棉子糖使醛糖还原酶活性增加的程度与氯化钠相同。相比之下,尿素和甘油均未影响酶活性。氯化钠和棉子糖导致细胞含水量持续下降,细胞钠和钾浓度增加,但尿素没有。在一些实验中,无论渗透压是否升高都添加哇巴因。综合考虑所有有或没有哇巴因的实验,我们发现醛糖还原酶活性单独与细胞钠浓度或细胞含水量均无相关性。然而,它确实与细胞钾浓度相关,并且与细胞钠加钾浓度的总和相关性更强。我们得出结论,高渗引发醛糖还原酶活性增加的信号很可能涉及细胞内离子强度的增加。

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