Farag M M, Volicer L
Pharmacology. 1985;31(6):309-17. doi: 10.1159/000138139.
Acute hepatic damage in centrilobular or periportal areas was induced in two groups of rats by intraperitoneal injections of bromobenzene or allyl alcohol, respectively. The effect of this zonal damage on the demethylation of 14C-aminopyrine was evaluated by measuring the elimination of 14CO2 in breath following intravenous administration of a tracer dose of the labeled compound. In rats with centrilobular hepatic damage 14CO2 elimination in breath was significantly decreased compared to controls. In rats with periportal hepatic damage, elimination of 14CO2 in breath was unchanged. These results suggest functional heterogeneity of hepatocytes in vivo with respect to drug-metabolizing capacity.
分别通过腹腔注射溴苯或烯丙醇,在两组大鼠中诱导小叶中央或门静脉周围区域的急性肝损伤。通过在静脉注射示踪剂量的标记化合物后测量呼出气体中¹⁴CO₂的排出量,评估这种区域性损伤对¹⁴C-氨基比林去甲基化的影响。与对照组相比,小叶中央肝损伤大鼠呼出气体中¹⁴CO₂的排出量显著降低。门静脉周围肝损伤大鼠呼出气体中¹⁴CO₂的排出量未发生变化。这些结果表明,体内肝细胞在药物代谢能力方面存在功能异质性。