Tamai I, Tsuji A
J Antibiot (Tokyo). 1987 Apr;40(4):533-41. doi: 10.7164/antibiotics.40.533.
The metabolism of benzylpenicillin (PCG) in isolated rat hepatocytes was investigated. The evidence of metabolizing activity for PCG in hepatic cells was obtained as follows; the disappearance rate of PCG from the incubation medium followed Michaelis-Menten kinetics and was dependent on the cellular protein concentration, while PCG did not disappear when it was incubated with cells denaturated by heat. The rate of disappearance of PCG was reduced significantly in the presence of the structural analogue of PCG such as phenoxymethylpenicillin in the incubation medium. The major metabolite of PCG was identified, by high performance liquid chromatographic analysis, to be penicilloic acid (PA) of PCG. A kinetic model describing the intra- and extra-cellular concentrations of PCG and PA was developed. The proposed model fitted well the time course of changes in the concentration of PCG and PA. The clearance of the uptake of PCG by isolated hepatocytes was evaluated to be about 23-times greater than that of metabolism of PCG.
研究了苄青霉素(PCG)在离体大鼠肝细胞中的代谢情况。获得肝细胞中PCG代谢活性的证据如下:PCG从孵育培养基中的消失速率遵循米氏动力学,并且取决于细胞蛋白浓度,而当PCG与经热变性的细胞一起孵育时,PCG不会消失。在孵育培养基中存在PCG的结构类似物(如苯氧甲基青霉素)时,PCG的消失速率显著降低。通过高效液相色谱分析鉴定出PCG的主要代谢产物是PCG的青霉酸(PA)。建立了一个描述PCG和PA细胞内和细胞外浓度的动力学模型。所提出的模型很好地拟合了PCG和PA浓度变化的时间进程。评估离体肝细胞对PCG的摄取清除率比PCG的代谢清除率大约高23倍。