Sótonyi P T, Csaba G
Institute of Biology, Semmelweis University of Medicine Budapest, Hungary.
Acta Morphol Hung. 1987;35(1-2):19-30.
The synthetic steroid diethylstilbestrol (DES) and the steroid-like allylestrenol (AE) have been used for years in human medicine for the protection of pregnancy. The hazards to the fetus of gestational DES treatment are well established [2, 17, 18]. Knowledge of a similar effect of AE is still fragmentary. Therefore, further studies are required of the after-effects of embryonic and perinatal AE exposure. In our earlier experiments with polypeptide hormones [4, 5, 6] we have observed that perinatal age is a critical period in the maturation of hormone receptors. In this period the presence of hormone induces the development of its specific receptors. The phenomenon is termed hormonal imprinting [4, 5, 6]. During its maturation the receptor is flexible and the presence of non-specific hormones capable of binding to it may alter its normal development Accordingly, even a single hormone injection in the perinatal period may alter the hormone-sensitivity of the target organ.
合成类固醇己烯雌酚(DES)和类固醇样烯丙雌醇(AE)多年来一直用于人类医学中以保护妊娠。孕期使用DES对胎儿的危害已得到充分证实[2,17,18]。关于AE类似作用的了解仍然不完整。因此,需要进一步研究胚胎期和围生期接触AE的后遗症。在我们早期关于多肽激素的实验[4,5,6]中,我们观察到围生期是激素受体成熟的关键时期。在此期间,激素的存在会诱导其特异性受体的发育。这种现象被称为激素印记[4,5,6]。在其成熟过程中,受体具有可塑性,能够与之结合的非特异性激素的存在可能会改变其正常发育。因此,即使在围生期单次注射激素也可能改变靶器官的激素敏感性。