Zelinski-Wooten M B, Hess D L, Baughman W L, Molskness T A, Wolf D P, Stouffer R L
Division of Reproductive Sciences, Oregon Regional Primate Research Center, Beaverton 97006.
J Clin Endocrinol Metab. 1993 Apr;76(4):988-95. doi: 10.1210/jcem.76.4.8473415.
Local modulation of follicular and gametogenic functions by ovarian androgens and estrogens in mammalian species has been proposed. This study examined the effects of elevated androgen/estrogen ratios during follicular maturation in vivo by inhibiting aromatase activity in rhesus monkeys. To obviate steroid feedback effects, gonadotropin-treated animals were used. Beginning at menses (day 1), animals received human (h) FSH (60 IU/day, im) on days 1-6, followed by hFSH plus hLH (60 IU/day, im) on days 7-9 to promote the growth of multiple follicles. Ovulatory maturation was induced by hCG (1000 IU, im) on day 10. On days 8-10, four animals received an aromatase inhibitor, 1,4,6-androstatrien-3,17-dione (ATD; 1-1.25 g, orally, twice/day), while five served as controls and received no further treatment. Within 8 h of ATD treatment, a 63% reduction in serum estradiol levels relative to control values was evident, which reached maximal suppression (84%) by day 10. A marked elevation (17-fold) in serum androstenedione and a lesser increase (2.6-fold) in serum testosterone occurred with aromatase inhibition, yielding androstenedione/estradiol (18.0) and testosterone/estradiol (1.9) ratios greater than those in controls (0.6 and 0.3, respectively). ATD treatment did not alter follicular diameters or the total number of follicles per animal (20 +/- 3) relative to control values (16 +/- 3). Of the total cohort classified, the proportion of oocytes collected at prophase I was greater (P < 0.05) after ATD treatment (31%) than in controls (11%). Completion of oocyte meiosis to metaphase II was retarded (P < 0.05) in ATD-treated (4%) compared to control (26%) animals. Furthermore, the in vitro fertilization rate of metaphase II oocytes from ATD-treated animals (9%) was reduced (P < 0.05) relative to that in controls (25%). While basal progesterone production by luteinizing granulosa cells in vitro was similar between groups, the addition of hCG in vitro enhanced progesterone secretion by cells from ATD-treated animals (3.1 +/- 0.3-fold over basal) to a greater extent (P = 0.05) than in controls (1.5 +/- 0.3-fold). Progesterone receptor was detected by immunocytochemistry in nuclei of luteinizing granulosa cells from ATD-treated animals as well as controls. Serum progesterone profiles and the length of the luteal phase were similar between groups. Thus, acute elevation of serum androgen/estrogen ratios in vivo during follicular maturation was detrimental to the gametogenic functions of the primate follicle, but did not alter follicular growth, events of early luteinization, or subsequent luteal function.(ABSTRACT TRUNCATED AT 400 WORDS)
已有研究提出,哺乳动物体内卵巢雄激素和雌激素对卵泡及配子发生功能存在局部调节作用。本研究通过抑制恒河猴体内芳香化酶活性,检测了卵泡成熟过程中雄激素/雌激素比值升高的影响。为避免类固醇反馈效应,使用了促性腺激素处理的动物。从月经周期第1天开始,动物在第1 - 6天接受人促卵泡激素(hFSH,60 IU/天,肌肉注射),随后在第7 - 9天接受hFSH加hLH(60 IU/天,肌肉注射)以促进多个卵泡生长。第10天通过注射人绒毛膜促性腺激素(hCG,1000 IU,肌肉注射)诱导排卵成熟。在第8 - 10天,4只动物接受芳香化酶抑制剂1,4,6 - 雄甾三烯 - 3,17 - 二酮(ATD;1 - 1.25 g,口服,每日两次),5只作为对照未接受进一步处理。在ATD处理后8小时内,血清雌二醇水平相对于对照值明显降低63%,到第10天达到最大抑制水平(84%)。芳香化酶抑制导致血清雄烯二酮显著升高(17倍),血清睾酮轻度升高(2.6倍),雄烯二酮/雌二醇(18.0)和睾酮/雌二醇(1.9)比值高于对照(分别为0.6和0.3)。ATD处理相对于对照值未改变卵泡直径或每只动物卵泡总数(20±3与16±3)。在所有分类的卵泡中,ATD处理后处于减数分裂前期I的卵母细胞比例(31%)高于对照(11%)(P < 0.05)。与对照动物(26%)相比,ATD处理动物(4%)的卵母细胞减数分裂完成至中期II受到阻碍(P < 0.05)。此外,ATD处理动物的中期II卵母细胞体外受精率(9%)相对于对照(25%)降低(P < 0.05)。虽然体外培养时两组黄体化颗粒细胞基础孕酮分泌相似,但体外添加hCG后,ATD处理动物细胞的孕酮分泌增强程度(比基础水平高3.1±0.3倍)大于对照(1.5±0.3倍)(P = 0.05)。通过免疫细胞化学在ATD处理动物及对照动物的黄体化颗粒细胞核中检测到孕酮受体。两组血清孕酮水平及黄体期长度相似。因此,卵泡成熟过程中体内血清雄激素/雌激素比值的急性升高对灵长类卵泡的配子发生功能有害,但不影响卵泡生长、早期黄体化过程或随后的黄体功能。(摘要截选至400字)