Wolkoff A W, Goresky C A, Sellin J, Gatmaitan Z, Arias I M
Am J Physiol. 1979 Jun;236(6):E638-48. doi: 10.1152/ajpendo.1979.236.6.E638.
Multiple-indicator dilution studies of labeled bilirubin uptake were carried out on isolated perfused rat livers with variable ligandin concentrations (from normal and thyroidectomized animals with and without phenobarbital pretreatment). Ligandin concentrations, measured immunologically, increased 25% after thyroidectomy and approximately doubled after phenobarbital pretreatment but decreased to normal during perfusion in the thyroidectomized nonpretreated group. A distributed two-compartment model was fitted to the dilution data and estimates of influx, efflux, and sequestration coefficients were obtained. Influx and sequestration coefficients did not vary significantly between the groups. Efflux coefficients were significantly smaller (P less than 0.001), and hepatic ligandin concentrations were significantly larger (p less than 0.001) in phenobarbital-treated rats than in other groups. The efflux coefficient varied inversely with ligandin concentration and the volume of distribution in tissue, as perceived from the plasma space, increased in proportion to the concentration of ligandin. The increased net uptake of tracer bilirubin by the liver of phenobarbital-pretreated animals is due to decreased tracer efflux secondary to the increase in intracellular binding of bilirubin by ligandin.
采用多指标稀释法对不同配体结合蛋白浓度(来自正常及甲状腺切除的动物,有无苯巴比妥预处理)的离体灌注大鼠肝脏进行标记胆红素摄取研究。通过免疫法测定的配体结合蛋白浓度,在甲状腺切除后增加25%,在苯巴比妥预处理后约增加一倍,但在未预处理的甲状腺切除组灌注过程中降至正常水平。对稀释数据拟合了一个分布式双室模型,并获得了流入、流出和滞留系数的估计值。各实验组间流入和滞留系数无显著差异。苯巴比妥处理大鼠的流出系数显著更小(P<0.001),肝脏配体结合蛋白浓度显著更高(P<0.001)。流出系数与配体结合蛋白浓度呈负相关,从血浆空间观察,组织中的分布容积与配体结合蛋白浓度成正比增加。苯巴比妥预处理动物肝脏对示踪胆红素净摄取的增加是由于配体结合蛋白增加了胆红素的细胞内结合,导致示踪剂流出减少。