Nishida K, Tonegawa C, Kakutani T, Hashida M, Sezaki H
Department of Basic Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.
Pharm Res. 1989 Feb;6(2):140-6. doi: 10.1023/a:1015980525940.
A new experimental system was applied to study hepatobiliary transport of drugs. Rat livers were perfused using a single-pass technique, and phenol red was momentarily introduced to this system from the portal side. Outflow dilution patterns of phenol red were analyzed using statistical moment theory, and kinetic parameters of hepatic distribution and elimination of phenol red were calculated from moments, namely, the hepatic extraction ratio (Ei) and elimination rate constant (kel,i). A larger distribution volume (Vi) was obtained for phenol red than for 131I-human serum albumin (HSA) and 51Cr-red blood cells (RBC), indicating its extravascular diffusivity. The biliary excretion of conjugated phenol red was delayed relative to that of the free agent. The larger biliary mean transit time (tbile,conj.) represents the processes of biliary transport and intrahepatic metabolism. Further, the effects of dose and perfusion temperature on the hepatobiliary transport of phenol red were determined. With high doses or low perfusion temperatures (20 and 27 degrees C), Ei, kel,i, and intrinsic clearance (CLint,i) of phenol red and biliary recovery of free and conjugated phenol red (Fbile,free, Fbile,conj) significantly decreased. The temperature-dependent and saturable processes in hepatic uptake, metabolism, and biliary excretion of phenol red were assessable to moment analysis.
一种新的实验系统被应用于研究药物的肝胆转运。使用单通道技术灌注大鼠肝脏,并从门静脉侧瞬间向该系统引入酚红。利用统计矩理论分析酚红的流出稀释模式,并从矩中计算酚红肝脏分布和消除的动力学参数,即肝脏提取率(Ei)和消除速率常数(kel,i)。与131I-人血清白蛋白(HSA)和51Cr-红细胞(RBC)相比,酚红获得了更大的分布容积(Vi),表明其血管外扩散性。结合型酚红的胆汁排泄相对于游离型酚红有所延迟。较大的胆汁平均转运时间(tbile,conj.)代表胆汁转运和肝内代谢过程。此外,还确定了剂量和灌注温度对酚红肝胆转运的影响。在高剂量或低灌注温度(20和27摄氏度)下,酚红的Ei、kel,i和内在清除率(CLint,i)以及游离型和结合型酚红的胆汁回收率(Fbile,free、Fbile,conj)显著降低。酚红肝脏摄取、代谢和胆汁排泄中温度依赖性和饱和性过程可通过矩分析进行评估。