Naish S J, Ball P
Neuroendocrinology. 1981 Apr;32(4):225-8. doi: 10.1159/000123163.
The ability of the catecholestrogens, 4-hydroxyestradiol (4-OHE2) and 2-hydroxyestradiol (2-OHE2) to induce lordosis in ovariectomized rats primed with progesterone was assessed following either short- or long-term exposure to the steroids. 4-OHE2 successfully induced lordosis whether administered as two bolus intrajugular injections separated by a 3-hour interval or continuously for 7 days via subcutaneously implanted osmotic minipumps. 2-OHE2, however, was ineffective under both conditions. When administered subcutaneously in conjunction with 3 days of estradiol benzoate (E2B) treatment, neither of the catecholestrogens exhibited any antiestrogenic effect as compared with the lordosis response to E2B alone. Likewise, simultaneous administration of 2-OHE2 did not significantly alter the response to intrajugular injections of estradiol (E2) or 4-OHE2. The results indicate that 4-OHE2 (but not 2-OHE2) mimicks the lordosis-inducing action of E2 and that neither catecholestrogen has any antiestrogenic effect in this behavioral test system.
在对用孕酮预处理的去卵巢大鼠进行短期或长期类固醇暴露后,评估了儿茶酚雌激素、4-羟基雌二醇(4-OHE2)和2-羟基雌二醇(2-OHE2)诱导脊柱前凸的能力。4-OHE2无论是通过间隔3小时的两次颈内静脉推注给药,还是通过皮下植入渗透微型泵连续给药7天,都能成功诱导脊柱前凸。然而,2-OHE2在这两种条件下均无效。当与3天的苯甲酸雌二醇(E2B)治疗联合皮下给药时,与单独对E2B的脊柱前凸反应相比,两种儿茶酚雌激素均未表现出任何抗雌激素作用。同样,同时给予2-OHE2并未显著改变对颈内静脉注射雌二醇(E2)或4-OHE2的反应。结果表明,4-OHE2(而非2-OHE2)模拟了E2诱导脊柱前凸的作用,并且在该行为测试系统中,两种儿茶酚雌激素均无任何抗雌激素作用。