Tse S S, Edmonds B, Mamelok R D
Biochim Biophys Acta. 1985 Apr 11;814(2):333-40. doi: 10.1016/0005-2736(85)90453-5.
In renal basal-lateral membranous vesicles, the probenecid-sensitive p-aminohippurate uptake was stimulated by alloxan. This stimulation of uptake was observed only after a lag period of 15 seconds, and it reached a maximal value after one minute. Stimulation was increased by 1 mM to 5 mM alloxan in a linear fashion. The effect was maximal and constant between 5 mM and 20 mM alloxan. Alloxan affected neither the glucose space of the vesicle nor the rate of transport or diffusion of glutamate, another organic anion. The mechanism of stimulation by alloxan was not clear. Its effect was blocked by the sulfhydryl reagent N-ethylmaleimide and weakly mimicked by H2O2, an oxidizing reagent. However, ninhydrin, a structural analogue of alloxan which reacts with sulfhydryl groups, and glucose, a neutral structural analogue of alloxan, failed to stimulate probenecid-sensitive uptake.
在肾基底外侧膜囊泡中,丙磺舒敏感的对氨基马尿酸摄取受到四氧嘧啶的刺激。这种摄取刺激仅在15秒的延迟期后才观察到,并且在1分钟后达到最大值。1 mM至5 mM的四氧嘧啶以线性方式增加刺激作用。在5 mM至20 mM的四氧嘧啶之间,该作用最大且恒定。四氧嘧啶既不影响囊泡的葡萄糖空间,也不影响另一种有机阴离子谷氨酸的转运或扩散速率。四氧嘧啶的刺激机制尚不清楚。其作用被巯基试剂N-乙基马来酰亚胺阻断,并且被氧化试剂过氧化氢微弱模拟。然而,与巯基反应的四氧嘧啶结构类似物茚三酮以及四氧嘧啶的中性结构类似物葡萄糖未能刺激丙磺舒敏感的摄取。