Gallo M A, Hesse E J, Macdonald G J, Umbreit T H
Toxicol Lett. 1986 Jul-Aug;32(1-2):123-32. doi: 10.1016/0378-4274(86)90058-5.
Weanling C57B/6 female mice treated with 6 micrograms/kg 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) 3 times a week for one month (total dose 72 micrograms/kg) were observed to have greatly reduced relative uterine weights and histopathological changes in the uterus. Weanling CD-1 female mice were then treated with estradiol (E2) subcutaneously daily for 2 weeks. Half the mice also received 10 micrograms/kg TCDD in corn oil: acetone (9:1) by gavage 4 times during the second week. Control mice received either no E2 or no TCDD. Mice were killed on day 15 and autopsied. Relative uterine weights increased with increasing E2 doses; however, TCDD decreased this effect of E2 markedly. Liver microsomes from these animals showed that cytochrome P1-450 and P3-450 and, aryl hydrocarbon hydroxylase (AHH) induction by TCDD were independent of E2 dosage. Epoxide hydrolase was induced in TCDD treated animals. Gels showed an E2 dose dependent decrease in a protein migrating near epoxide hydrolase and 'P-450a' in animals receiving both E2 and TCDD. These results suggest that: E2 may act at the TCDD receptor; the TCDD receptor may be related to the estrogen receptor; the anti-estrogenic effects of TCDD are possibly independent of the Ah locus and AHH induction, and in TCDD-treated mice a protein migrating near epoxide hydrolase and 'P-450a' may be controlled by estrogen levels.
对断乳的C57B/6雌性小鼠,每周3次给予6微克/千克2,3,7,8-四氯二苯并对二恶英(TCDD),持续1个月(总剂量72微克/千克),观察到其子宫相对重量大幅降低且子宫出现组织病理学变化。然后对断乳的CD-1雌性小鼠每天皮下注射雌二醇(E2),持续2周。在第二周,一半小鼠还通过灌胃给予10微克/千克TCDD(溶于玉米油:丙酮,比例为9:1),共4次。对照小鼠既不给予E2也不给予TCDD。在第15天处死小鼠并进行尸检。子宫相对重量随E2剂量增加而增加;然而,TCDD显著降低了E2的这种作用。这些动物的肝脏微粒体显示,TCDD对细胞色素P1 - 450和P3 - 450以及芳烃羟化酶(AHH)的诱导与E2剂量无关。在TCDD处理的动物中诱导了环氧水解酶。凝胶显示,在同时接受E2和TCDD的动物中,靠近环氧水解酶和“P - 450a”迁移的一种蛋白质呈E2剂量依赖性减少。这些结果表明:E2可能作用于TCDD受体;TCDD受体可能与雌激素受体相关;TCDD的抗雌激素作用可能独立于Ah位点和AHH诱导,并且在TCDD处理的小鼠中,靠近环氧水解酶和“P - 450a”迁移的一种蛋白质可能受雌激素水平控制。