Fleck C, Bräunlich H
Institute of Pharmacology and Toxicology, Friedrich Schiller University, Jena, German Democratic Republic.
Arzneimittelforschung. 1990 Sep;40(9):1047-53.
The relation between renal and biliary excretion of drugs was investigated in dependence on physicochemical factors, on age, and on repeated administration of hormones and xenobiotics for stimulation. Furthermore, the relation between molecular parameters of drugs and the degree of compensation of drug elimination after blockade of one excretion pathway (nephrectomy--NX, bile duct ligation--DL) was characterized. Experiments were performed on female 20-day and 55-day-old rats to demonstrate changes in the relationship between kidney and liver for drug elimination during ontogenesis. Finally it was tried to correlate the effect of a stimulation of elimination capacity of kidney and liver after repeated administration of hormones or xenobiotics and the physicochemical features of clearance substances tested. For estimation of physicochemical differences of the model substances a so called "rank coefficient" R (0-100) was used. It was calculated from molecular weight, lipophilicity, degree of ionization at pH 7.4, and protein binding rate. Compounds with low ranks (low values of molecular weight, lipophilicity, and protein binding, nearly completely ionic at pH 7.4) are eliminated first of all via urine. High ranks are typical of drugs preferentially eliminated into bile. Intermediate ranks (40-60) have been obtained for substances eliminated effectively both via kidney and liver. For these compounds only, a distinct compensation via the intact elimination route can be expected after blocking operations. Qualitative age differences could not be found. But there were differences concerning relation between acceleration of transport capacity of kidney and liver during postnatal maturation and physicochemical properties of the respective test substance.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了药物的肾排泄和胆汁排泄之间的关系,该关系取决于物理化学因素、年龄以及激素和外源化合物的重复给药刺激。此外,还对药物的分子参数与一种排泄途径被阻断(肾切除——NX,胆管结扎——DL)后药物消除的代偿程度之间的关系进行了表征。在20日龄和55日龄的雌性大鼠身上进行实验,以证明在个体发育过程中肾脏和肝脏在药物消除方面关系的变化。最后,试图将激素或外源化合物重复给药后肾脏和肝脏消除能力的刺激效果与所测试清除物质的物理化学特征联系起来。为了评估模型物质的物理化学差异,使用了一种所谓的“秩系数”R(0 - 100)。它由分子量、亲脂性、pH 7.4时的电离程度和蛋白结合率计算得出。低秩的化合物(分子量、亲脂性和蛋白结合值低,在pH 7.4时几乎完全离子化)首先通过尿液消除。高秩是优先排入胆汁的药物的典型特征。中等秩(40 - 60)是通过肾脏和肝脏都能有效消除的物质所具有的。只有对于这些化合物,在阻断操作后才有望通过完整的消除途径实现明显的代偿。未发现定性的年龄差异。但在出生后成熟过程中肾脏和肝脏转运能力的加速与各自测试物质的物理化学性质之间的关系存在差异。(摘要截断于250字)