Ormstad K, Uehara N
FEBS Lett. 1982 Dec 27;150(2):354-8. doi: 10.1016/0014-5793(82)80767-9.
The transport and reduction of dimesna (Na-2-mercaptoethane sulfonate disulfide) was studied in vitro using isolated, perfused rat kidney, and isolated renal epithelial cells. Cellular uptake of dimesna was found to be dependent on an active transport mechanism working across the luminal brush border, with an app. Km of approximately 22 microM and Vmax approximately 1.4 nmol . 10(6) cells-1 . min-1. Among other low molecular thiols or disulfides reduced glutathione was the only one to exert competitive inhibition. gamma-GT-activity or cellular GSH status had no influence on renal uptake of dimesna, but the intracellular reduction rate was dependent on access to reduced glutathione as a cofactor.
使用离体灌流大鼠肾脏和离体肾上皮细胞,在体外研究了二巯基丁二酸钠(Na - 2 - 巯基乙烷磺酸钠二硫化物)的转运和还原。发现二巯基丁二酸钠的细胞摄取依赖于一种跨管腔刷状缘起作用的主动转运机制,其表观Km约为22微摩尔,Vmax约为1.4纳摩尔·10⁶个细胞⁻¹·分钟⁻¹。在其他低分子硫醇或二硫化物中,还原型谷胱甘肽是唯一能发挥竞争性抑制作用的物质。γ - GT活性或细胞内谷胱甘肽状态对二巯基丁二酸钠的肾脏摄取没有影响,但细胞内还原速率取决于作为辅因子的还原型谷胱甘肽的可及性。