Andreyko J L, Monroe S E, Marshall L A, Fluker M R, Nerenberg C A, Jaffe R B
Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco 94143.
J Clin Endocrinol Metab. 1992 Feb;74(2):399-405. doi: 10.1210/jcem.74.2.1370507.
The purposes of the current study were 2-fold: 1) to assess the effects of a new antagonistic analog of GnRH [N-Ac-D-Nal(2)1, D-pC1-phe2, D-Trp3, D-hArg (Et2)6, D-Ala10] GnRH, or detirelix (Syntex Research) on gonadotrope function as reflected by serum levels of immuno- and bioassayable LH, and immunoactive FSH and alpha-subunit concentrations in postmenopausal, hypergonadotropic women; and 2) to determine if androgen production in the postmenopausal ovary is gonadotropin dependent. Six normal postmenopausal women were studied. Each volunteer received doses of 1, 5, and 20 mg detirelix sc in a random order separated by at least a 1-week interval. Serum LH, FSH, and alpha-subunit were measured by RIA at frequent intervals for 72 h after each injection. Bioactive LH levels were measured at 0, 24, 48, and 72 h after injection by a mouse Leydig cell bioassay, to permit comparison of biological with immunological LH activity. The steroids testosterone (T) and dehydroepiandrosterone sulfate were measured before injection and 12 (T only), 24 and 48 h after injection of the 20 mg dose. Immunoactive levels of serum LH and FSH were both suppressed in a dose-dependent manner, but LH suppression was greater than that of FSH. Maximum LH suppression (mean +/- SEM) after the 1, 5, and 20 mg doses was 40.2 +/- 7.0%, 63.2 +/- 3.4%, and 75.8 +/- 2.2%, respectively. For the same doses, maximum FSH suppression was 18.0 +/- 6.0%, 25.6 +/- 4.6%, and 39.6 +/- 2.7%. LH levels remained suppressed below baseline for up to 72 h after the 20 mg dose. Bioactive LH changes closely paralleled those of immunoactive LH. Mean LH suppression (area under the serum concentration curve) during the first 24 h after injection was 23.5 +/- 6.2% for the 1-mg dose, 47.2 +/- 4.7% for the 5-mg dose, and 61.0 +/- 2.1% for the 20-mg dose. Mean percent FSH suppression during the first 24 h, calculated in the same manner, was 6.8 +/- 3.9% (1 mg), 14.5 +/- 2.9% (5 mg), and 18.2 +/- 2.6% (20 mg). Serum alpha-subunit concentrations were significantly suppressed by 1 h after dosing with the 5- and 20-mg doses (P less than 0.05), and remained suppressed throughout the 72-h sampling period. Gonadotropin dependence of steroidogenesis in the postmenopausal ovary was suggested by a significant suppression of serum T concentrations after the 20-mg dose of detirelix.(ABSTRACT TRUNCATED AT 400 WORDS)
1)评估一种新的促性腺激素释放激素(GnRH)拮抗类似物[N-乙酰-D-萘丙氨酸(2)1,D-对氯苯丙氨酸2,D-色氨酸3,D-高精氨酸(乙基)6,D-丙氨酸10]GnRH,即地瑞林(先灵葆雅研究所)对绝经后、高促性腺激素水平女性的促性腺激素细胞功能的影响,这可通过免疫法和生物测定法检测的血清促黄体生成素(LH)水平、免疫活性促卵泡生成素(FSH)和α亚基浓度来反映;2)确定绝经后卵巢中的雄激素生成是否依赖促性腺激素。对6名正常绝经后女性进行了研究。每位志愿者按随机顺序皮下注射1、5和20mg地瑞林,每次注射间隔至少1周。每次注射后72小时内频繁采集血清,用放射免疫分析法(RIA)测定LH、FSH和α亚基。在注射后0、24、48和72小时,通过小鼠睾丸间质细胞生物测定法测量生物活性LH水平,以便比较生物活性LH与免疫活性LH的活性。在注射20mg剂量前及注射后12小时(仅针对睾酮)、24小时和48小时测量类固醇睾酮(T)和硫酸脱氢表雄酮。血清LH和FSH的免疫活性水平均呈剂量依赖性抑制,但LH的抑制作用大于FSH。1、5和20mg剂量后的最大LH抑制率(平均值±标准误)分别为40.2±7.0%、63.2±3.4%和75.8±2.2%。对于相同剂量,最大FSH抑制率分别为18.0±6.0%、25.6±4.6%和39.6±2.7%。20mg剂量后,LH水平在72小时内一直被抑制在基线以下。生物活性LH的变化与免疫活性LH密切平行。注射后第1个24小时内,1mg剂量的平均LH抑制率(血清浓度曲线下面积)为23.5±6.2%,5mg剂量为47.2±4.7%,20mg剂量为61.0±2.1%。以同样方式计算,第1个24小时内FSH的平均抑制率分别为6.8±3.9%(1mg)、14.5±2.9%(5mg)和18.2±2.6%(20mg)。给予5mg和20mg剂量后1小时,血清α亚基浓度即被显著抑制(P<0.05),并在整个72小时采样期内持续被抑制。20mg剂量的地瑞林显著抑制血清T浓度,提示绝经后卵巢中类固醇生成依赖促性腺激素。(摘要截选至400字)