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肾脏刷状缘膜中的硫醇氧化还原与磷酸盐转运。烟酰胺的作用。

Thiol redox and phosphate transport in renal brush-border membrane. Effect of nicotinamide.

作者信息

Suzuki M, Capparelli A W, Jo O D, Yanagawa N

机构信息

Division of Nephrology, Veterans Administration Sepulveda Hospital, CA 91343.

出版信息

Biochim Biophys Acta. 1990 Jan 15;1021(1):85-90. doi: 10.1016/0005-2736(90)90388-5.

Abstract

In the present study, the effect of thiol redox and its possible role in the inhibitory effect of nicotinamide on renal brush-border membrane (BBM) phosphate uptake was examined. Addition of thiol reducing agent, dithiothreitol (DTT, 5 mM), caused an increase, while addition of thiol oxidant, diamide (DM, 5 mM) caused a reversible decrease in sodium-dependent BBM phosphate uptake. Kinetic analyses revealed an increase in both Vmax and Km by DTT, and a decrease in Vmax by DM. These results suggest that thiol redox influences BBM phosphate uptake with sulfhydryl (SH) groups relate to its capacity and disulfide (SS) groups to its affinity for phosphate. Since changes in cytosolic NAD levels may affect BBM thiol redox through changes in redox states of NADP and glutathione systems, we have examined such possibility by studying the effect of nicotinamide (NM). Incubation of proximal tubules with NM (10 mM) induced an oxidative effect on redox states of cytosolic NAD, NADP systems as inferred from decreased cellular lactate/pyruvate, malate/pyruvate, respectively. Measurements of cytosolic glutathiones and BBM thiols also revealed that NM pretreatment shifted the cytosolic glutathione redox (GSH/GSSG) and BBM thiol redox (SH/SS) toward more oxidized state. On the other hand, incubation of proximal tubules with NM suppressed phosphate uptake by the subsequently isolated BBM vesicles. The lower phosphate uptake by NM-pretreated BBM vesicles was reversed by DTT and was resistant to the inhibitory effect of DM. These results thus suggest that BBM thiol oxidation may be involved in the inhibitory effect of NM on BBM phosphate uptake.

摘要

在本研究中,检测了硫醇氧化还原的作用及其在烟酰胺对肾刷状缘膜(BBM)磷酸盐摄取的抑制作用中可能发挥的作用。添加硫醇还原剂二硫苏糖醇(DTT,5 mM)会导致增加,而添加硫醇氧化剂二酰胺(DM,5 mM)会使钠依赖性BBM磷酸盐摄取出现可逆性降低。动力学分析显示,DTT使Vmax和Km均增加,而DM使Vmax降低。这些结果表明,硫醇氧化还原影响BBM磷酸盐摄取,巯基(SH)基团与其摄取能力有关,二硫键(SS)基团与其对磷酸盐的亲和力有关。由于胞质NAD水平的变化可能通过NADP和谷胱甘肽系统氧化还原状态的改变来影响BBM硫醇氧化还原,因此我们通过研究烟酰胺(NM)的作用来检验这种可能性。用NM(10 mM)孵育近端小管对胞质NAD、NADP系统的氧化还原状态产生了氧化作用,这分别从细胞乳酸/丙酮酸、苹果酸/丙酮酸的降低推断得出。对胞质谷胱甘肽和BBM硫醇的测量还显示,NM预处理使胞质谷胱甘肽氧化还原(GSH/GSSG)和BBM硫醇氧化还原(SH/SS)向更氧化的状态转变。另一方面,用NM孵育近端小管会抑制随后分离的BBM囊泡对磷酸盐的摄取。DTT可逆转NM预处理的BBM囊泡较低的磷酸盐摄取,且该摄取对DM的抑制作用具有抗性。因此,这些结果表明BBM硫醇氧化可能参与了NM对BBM磷酸盐摄取的抑制作用。

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