Denton J E, Potter G D, Santolucito J A
J Toxicol Environ Health. 1981 Jun;7(6):893-900. doi: 10.1080/15287398109530032.
The possibility that Pb could affect benzene metabolism, through inhibition of enzyme synthesis, was examined by studies of the effects of chronic oral Pb treatments on benzene conversion to phenol. Rats were given either distilled deionized water or 0.05, 0.58, 17, or 352 ppm Pb solutions as drinking water. After 6, 9, 12, and 15 wk of treatment, rats from each group were sacrificed and in vitro benzene metabolism by benzene hydroxylase was measured in liver enzyme preparations. After 24 wk, the remaining animals were injected ip with 400 mg/kg benzene and urinary phenol levels measured daily for 4 d. The enzyme activity, studied in vitro, was significantly increased in animals that ingested the 352 ppm solution for 6 wk. Also, Pb levels in all groups of animals were significantly higher in tissues from the animals that ingested 352 ppm Pb. Although urinary phenol levels accounted for 30-40% of the ip benzene dose, Pb ingestion had no significant effect on phenol excretion. These results suggested that oral Pb treatments had a significant effect on the enzyme responsible for benzene hydroxylation to phenol. However, other unknown factors appear to compensate for these changes in vivo.
通过研究慢性口服铅处理对苯转化为苯酚的影响,检验了铅是否可能通过抑制酶的合成来影响苯代谢。给大鼠饮用蒸馏水或浓度为0.05、0.58、17或352 ppm的铅溶液。处理6、9、12和15周后,处死每组大鼠,在肝脏酶制剂中测量苯羟化酶的体外苯代谢情况。24周后,给剩余动物腹腔注射400 mg/kg苯,并连续4天每天测量尿中苯酚水平。体外研究的酶活性在摄入352 ppm溶液6周的动物中显著增加。此外,摄入352 ppm铅的动物组织中所有组的铅水平均显著更高。尽管尿中苯酚水平占腹腔注射苯剂量的30 - 40%,但摄入铅对苯酚排泄没有显著影响。这些结果表明,口服铅处理对负责将苯羟化为苯酚的酶有显著影响。然而,其他未知因素似乎在体内补偿了这些变化。