Söderkvist P, Toftgard R, Gustafsson J A
Toxicol Lett. 1982 Jan;10(1):61-9. doi: 10.1016/0378-4274(82)90268-5.
Rats were treated with beta-naphthoflavone (BNF) or phenobarbital (PB), 80 mg/kg i.p. for 4 days and microsomes prepared from the ventral prostate were assayed for aryl hydrocarbon hydroxylase (AHH), 7-ethoxyresorufin-o-deethylase (7-EOD) and NADPH-cytochrome c reductase activities. The relative increase after BNF treatment was approx. 1000 times for AHH, and 800 times for 7-EOD, while the NADPH-cytochrome c reductase activity was not significantly altered. PB treatment caused no significant effects. Treatment with BNF led to an increased in vitro formation of all measured benzo(a)pyrene (B(a)P) metabolites, especially phenols. Carbon monoxide (CO) and alpha-naphthoflavone (alpha-NF) inhibited 7-EOD- and AHH-activities. The rat ventral prostate contains inducible cytochrome P-450-dependent enzymes, a circumstance of potential important in the etiology of prostatic carcinoma.
给大鼠腹腔注射80mg/kg的β-萘黄酮(BNF)或苯巴比妥(PB),持续4天,然后测定从腹侧前列腺制备的微粒体中芳烃羟化酶(AHH)、7-乙氧基异吩恶唑酮-O-脱乙基酶(7-EOD)和NADPH-细胞色素c还原酶的活性。BNF处理后,AHH的相对增加约为1000倍,7-EOD为800倍,而NADPH-细胞色素c还原酶活性没有显著改变。PB处理没有显著影响。BNF处理导致所有测定的苯并(a)芘(B(a)P)代谢产物,尤其是酚类的体外形成增加。一氧化碳(CO)和α-萘黄酮(α-NF)抑制7-EOD和AHH活性。大鼠腹侧前列腺含有可诱导的细胞色素P-450依赖性酶,这在前列腺癌的病因学中可能具有重要意义。