Begleiter A, Grover J, Goldenberg G J
Cancer Res. 1982 Mar;42(3):987-91.
The mechanism of efflux of melphalan from L5178Y lymphoblasts in vitro was investigated. Evidence was obtained that drug efflux occurs by a process different from the influx mechanism. A time course of efflux followed a first-order process for at least 5 min, with a rate constant K of 0.13 +/- 0.05 (S.D.) min-1, and approximately 80% of drug taken up by the cells was exchangeable. From a kinetic analysis of melphalan efflux, it was not possible to determine if the mechanism of drug efflux was simple diffusion or a technically nonsaturable carrier-mediated process. The Q10 for drug efflux varied from 1.2 to 1.8, values intermediate between those expected for simple diffusion and a carrier-mediated process. Furthermore, drug efflux was sodium independent and was not inhibited by the presence of amino acids on the same side of the membrane, findings which support the concept that efflux was by simple diffusion. The presence of a wide variety of amino acids in the extracellular medium was found to stimulate melphalan efflux. An evaluation of the structure-activity relationship disclosed that amino acids containing hydroxyl, acidic, or amide side chains were most active; however, a distinct pattern between amino acid structure and stimulation of efflux was not established. The stimulation process was concentration dependent and was not restricted to either L5178Y cells or to melphalan as transport substrate.
研究了美法仑在体外从L5178Y淋巴母细胞中流出的机制。有证据表明药物流出是通过一个与流入机制不同的过程发生的。流出的时间进程至少在5分钟内遵循一级过程,速率常数K为0.13±0.05(标准差)分钟⁻¹,细胞摄取的约80%的药物是可交换的。从美法仑流出的动力学分析中,无法确定药物流出机制是简单扩散还是技术上不可饱和的载体介导过程。药物流出的Q10在1.2至1.8之间变化,该值介于简单扩散和载体介导过程预期值之间。此外,药物流出不依赖于钠,并且不受膜同一侧氨基酸存在的抑制,这些发现支持流出是通过简单扩散的概念。发现细胞外培养基中存在多种氨基酸可刺激美法仑流出。对构效关系的评估表明,含有羟基、酸性或酰胺侧链的氨基酸活性最高;然而,氨基酸结构与流出刺激之间并未建立明显的模式。刺激过程是浓度依赖性的,并且不限于L5178Y细胞或美法仑作为转运底物。