Effect of simultaneous Tc-99m diethyl-IDA and sulfobromophthalein administration on liver excretory function in rats.

B Milutinović, F Dujmović, J Malesević
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Abstract

Competition of diethyl-IDA and BSP during their synchronous passage through the liver was examined on an animal model. Rats were divided in three groups, according to the amount of diethyl-IDA or BSP administered. No significant influence of diethyl-IDA on the liver uptake of BSP was noticed compared to the controls, while BSP demonstrated a significant inhibitory effect on diethyl-IDA plasma-activity decrease. On the biliary pole of hepatocyte, a reciprocal inhibitory influence of both compounds was present, with significantly diminished biliary excretion of both BSP and diethyl-IDA. As the input of BSP was not decreased, there evidently appeared a storage of BSP within the liver. A mathematical model of both plasma and bile changes of the concentration (or activity) of these compounds was also proposed. For the vascular compartment the model is correct, while biliary excretion of diethyl-IDA is significantly changed in presence of BSP and the satisfactory fit cannot be easily obtained.

同时给药Tc-99m二乙基ida和磺溴眼啡对大鼠肝脏排泄功能的影响。
用动物模型研究了二乙基ida和BSP在同步通过肝脏过程中的竞争。根据二乙基ida或BSP的剂量将大鼠分为三组。与对照组相比,二乙基- ida对肝脏对BSP的摄取没有显著影响,而BSP对二乙基- ida血浆活性下降有显著抑制作用。在肝细胞的胆道极,这两种化合物的相互抑制作用是存在的,BSP和二乙基- ida的胆汁排泄显著减少。由于BSP的输入没有减少,肝脏内明显出现了BSP的储存。还提出了血浆和胆汁中这些化合物浓度(或活性)变化的数学模型。对于血管腔室,模型是正确的,但BSP存在时,胆中二乙基- ida的排泄明显改变,难以获得满意的拟合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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