Johansson B
Department of Zoophysiology, Uppsala University, Sweden.
Pharmacol Toxicol. 1987 Oct;61(4):220-3. doi: 10.1111/j.1600-0773.1987.tb01807.x.
Male mice were exposed to two different preparations of PCBs. The pure congener 2,2',4,4',5,5'-hexachlorobiphenyl (6-CB) was given at daily doses of 4, 20, and 40 mg/kg b.wt. during the perinatal or pubertal period. A technical mixture of PCB (Clophen A50) was administered during puberty at daily doses of 8, 40, 80, 120, and 160 mg/kg b.wt. Treatments were, in the different experiments, carried out every second or third day for three to five weeks. Treatment during puberty was started when the mice were 5 weeks old. The perinatal exposure was started on day 13 of gestation and ended on day 24 post partum. There were no significant differences in the plasma levels of testosterone between the treated mice and the controls after any of the treatments, but there was an increase in the relative testes weights for the animals treated perinatally. No influence on the biosynthesis of testosterone in the testicular interstitial cells in vitro could be demonstrated.
雄性小鼠被暴露于两种不同的多氯联苯制剂中。在围产期或青春期,给予纯同系物2,2',4,4',5,5'-六氯联苯(6-CB),每日剂量分别为4、20和40毫克/千克体重。在青春期给予多氯联苯技术混合物(氯芬A50),每日剂量分别为8、40、80、120和160毫克/千克体重。在不同实验中,每隔一天或第三天进行一次处理,持续三至五周。青春期的处理在小鼠5周龄时开始。围产期暴露于妊娠第13天开始,产后第24天结束。在任何一种处理后,处理组小鼠与对照组小鼠的血浆睾酮水平均无显著差异,但围产期处理的动物睾丸相对重量增加。体外实验未证明对睾丸间质细胞睾酮生物合成有影响。