Hines M, Goy R W
Horm Behav. 1985 Sep;19(3):331-47. doi: 10.1016/0018-506x(85)90031-5.
Influences of estrogens on the differentiation of psychosexual traits in the female guinea pig were studied. Pregnant animals were injected intramuscularly with either 1, 2, or 3.3 micrograms estradiol benzoate (EB) or with 1 or 3 micrograms diethylstilbestrol dipropionate (DESDP). Injections were started on the 29th day of pregnancy, given daily for 6 days, and continued every other day until parturition. Female offspring were evaluated for onset of puberty, ovarian function, and lordosis and mounting behavior in adulthood. Prenatal treatment with 3 micrograms DESDP caused delayed puberty, impaired ovarian function, reduced responsiveness of lordosis to EB and P in adulthood (defeminization), augmented mounting in the absence of hormones (masculinization), and reduced responsiveness of mounting to exogenous EB and P in adulthood (defeminization). Prenatal treatment with 1 microgram DESDP produced similar but less pronounced effects. Prenatal treatment with 3.3 micrograms EB also caused a delay in puberty. However, responsiveness of lordosis to EB and P in adulthood was enhanced by treatment with either 1 or 3.3 micrograms EB prenatally. Further, neither mounting in the absence of hormones nor mounting in response to EB and P in adulthood were affected in any measurable way by any prenatal treatment with EB. These results show that estrogens can have masculinizing and defeminizing effects on sexually dimorphic reproductive traits in guinea pigs. The failure of EB to duplicate or parallel the effects of DESDP is not completely understood at this time, but it may indicate that less of the active substance reaches the target tissues following maternal and placental metabolism of EB than of DESDP.
研究了雌激素对雌性豚鼠心理性特征分化的影响。给怀孕动物肌肉注射1、2或3.3微克苯甲酸雌二醇(EB)或1或3微克己烯雌酚二丙酸酯(DESDP)。在怀孕第29天开始注射,每天注射1次,共注射6天,然后每隔一天注射1次,直至分娩。对雌性后代进行青春期开始时间、卵巢功能以及成年期脊柱前凸和骑跨行为的评估。产前用3微克DESDP治疗导致青春期延迟、卵巢功能受损、成年期脊柱前凸对EB和P的反应性降低(去雌性化)、在无激素情况下骑跨行为增加(雄性化)以及成年期骑跨行为对外源性EB和P的反应性降低(去雌性化)。产前用1微克DESDP治疗产生了类似但不太明显的效果。产前用3.3微克EB治疗也导致青春期延迟。然而,产前用1或3.3微克EB治疗可增强成年期脊柱前凸对EB和P的反应性。此外,产前用EB进行的任何治疗均未以任何可测量的方式影响无激素情况下的骑跨行为或成年期对EB和P的骑跨反应。这些结果表明,雌激素可对豚鼠两性异形的生殖特征产生雄性化和去雌性化作用。目前尚不完全清楚EB为何不能复制或与DESDP的作用平行,但这可能表明,与DESDP相比,EB经母体和胎盘代谢后到达靶组织的活性物质较少。