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绵羊红细胞中硫醇依赖性钾氯转运:VIII. 通过二酰胺进行代谢和化学可逆氧化激活。

Thiol-dependent K:Cl transport in sheep red cells: VIII. Activation through metabolically and chemically reversible oxidation by diamide.

作者信息

Lauf P K

机构信息

Department of Physiology and Biophysics, Wright State University, School of Medicine, Dayton, Ohio 45401-0927.

出版信息

J Membr Biol. 1988;101(2):179-88. doi: 10.1007/BF01872833.

Abstract

The sulfhydryl (SH) oxidant diamide activated in a concentration-dependent manner ouabain-resistant (OR), Cl-dependent K flux in both low potassium (LK) and high potassium (HK) sheep red cells as determined from the rate of zero-trans K efflux into media with Cl or Cl replaced by NO3 or methane sulfonate (CH3SO3). Diamide did not alter the OR Na efflux into choline Cl. The diamide effect on K efflux appeared after 80% of cellular glutathione (GSH) was oxidized to GSSG, its disulfide. The stimulation of K efflux was completely reversed during metabolic restitution of GSH, a process that depended on the length of exposure to and the concentration of diamide. The action of diamide on both the K:Cl transporter and GSH was also fully reversed by the reducing agent dithiothreitol (DTT). Diamide apparently oxidized the same SH groups alkylated by N-ethylmaleimide (NEM) (Lauf, P.K. 1983. J. Membrane Biol. 73:237-246). Like NEM, diamide activated K:Cl transport several-fold more in LK cells than in HK cells, and the effect on LK cells was partially inhibited by anti-L1, the allo-antibody known to inhibit OR K fluxes.

摘要

巯基(SH)氧化剂二酰胺以浓度依赖性方式激活了低血钾(LK)和高血钾(HK)绵羊红细胞中对哇巴因耐药(OR)的、依赖氯离子的钾离子通量,这是通过零转运钾离子外流到含有氯离子或氯离子被硝酸根或甲磺酸盐(CH3SO3)取代的培养基中的速率来确定的。二酰胺并未改变OR钠离子外流到氯化胆碱中的情况。二酰胺对钾离子外流的作用在80%的细胞谷胱甘肽(GSH)被氧化为其二硫化物GSSG后出现。在GSH的代谢恢复过程中,钾离子外流的刺激作用完全逆转,这一过程取决于暴露于二酰胺的时间长度和浓度。二酰胺对钾离子-氯离子转运体和GSH的作用也被还原剂二硫苏糖醇(DTT)完全逆转。二酰胺显然氧化了被N-乙基马来酰亚胺(NEM)烷基化的相同SH基团(Lauf,P.K.1983。《膜生物学杂志》73:237-246)。与NEM一样,二酰胺在LK细胞中激活钾离子-氯离子转运的倍数比在HK细胞中高几倍,并且对LK细胞的作用被已知可抑制OR钾离子通量的同种异体抗体抗-L1部分抑制。

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