Debets F M, Strik J J, Olie K
Toxicology. 1980;15(3):181-95. doi: 10.1016/0300-483x(80)90052-9.
Hexachlorobenzene (HCB, 1000 ppm) and 500 ppm pentachlorophenol (PCP) were fed separately or in combination to female Wistar rats. A control group was provided with standard food without HCB or PCP. Subgroups of 4 rats were killed after 1, 2, 4, 6 and 8 weeks. No significant difference was found between the amounts of HCB accumulated in the livers of the HCB and HCB + PCP fed rats. Administering HCB together with PCP caused a noticeable accumulation of PCP in the liver, compared to the results after administering HCB and PCP separately. In the HCB and HCB + PCP fed groups liver weight increased continuously during the experiments. Microsomal cytochrome P-450, NADPH-cytochrome c reductase, ethoxyresorufin O-de-ethylase, aminopyrine N-demethylase, and glucuronyl transferase increased to a maximum in 2-4 weeks in HCB and HCB + PCP fed rats. Pentachlorophenol accelerates the onset of HCB porphyria, in other words it increases the total urinary porphyrin excretion and causes an earlier disturbance of the porphyrin pattern.
将六氯苯(HCB,1000 ppm)和500 ppm五氯苯酚(PCP)分别或联合投喂给雌性Wistar大鼠。给一个对照组提供不含HCB或PCP的标准食物。在1、2、4、6和8周后处死4只大鼠的亚组。在投喂HCB的大鼠和投喂HCB + PCP的大鼠肝脏中积累的HCB量之间未发现显著差异。与分别投喂HCB和PCP后的结果相比,将HCB与PCP一起投喂会导致肝脏中PCP明显积累。在实验过程中,投喂HCB组和投喂HCB + PCP组的肝脏重量持续增加。在投喂HCB和HCB + PCP的大鼠中,微粒体细胞色素P - 450、NADPH - 细胞色素c还原酶、乙氧异吩唑酮O - 脱乙基酶、氨基比林N - 脱甲基酶和葡糖醛酸转移酶在2 - 4周时增加到最大值。五氯苯酚加速了HCB卟啉症的发作,换句话说,它增加了尿卟啉的总排泄量,并导致卟啉模式更早出现紊乱。