Hall J E, Whitcomb R W, Rivier J E, Vale W W, Crowley W F
Reproductive Endocrine Unit, Massachusetts General Hospital, Boston 02114.
J Clin Endocrinol Metab. 1990 Feb;70(2):328-35. doi: 10.1210/jcem-70-2-328.
To examine the differential regulation of glycoprotein hormone secretion from the gonadotrope by GnRH, the Nal-Glu GnRH antagonist was administered to euthyroid women in the early follicular phase (days 1-5) of the menstrual cycle, and the results compared to previous studies with the Nal-Arg GnRH antagonist. After a 4-h period of baseline sampling at a frequency of every 10 min, a single sc dose of the GnRH antagonist was administered to each subject. Frequent sampling continued for 8 h, followed by hourly sampling for a further 16 h. LH, FSH, and free alpha-subunit were measured serially in assays with high specificity. There was a 90% concordance of LH and free alpha-subunit pulses during the baseline sampling period. Pulsatile secretion of LH and free alpha-subunit was immediately abolished at the highest dose of the Nal-Glu antagonist for at least 8 h. The maximum percent suppression of LH after administration of the Nal-Glu GnRH antagonist was 70 +/- 4%, 80 +/- 4%, and 83 +/- 1% at doses of 15, 50, and 150 micrograms/kg, respectively, compared to 51 +/- 10%, 70 +/- 5%, and 69 +/- 5% at doses of 50, 150, and 500 micrograms/kg Nal-Arg antagonist. Decreases in FSH were 28 +/- 2%, 32 +/- 7%, and 39 +/- 2%, with increasing doses of the Nal-Glu antagonist compared with 25 +/- 6%, 17 +/- 6%, and 28 +/- 4% reductions at increasing doses of the Nal-Arg antagonist. Free alpha-subunit decreased 22 +/- 4%, 23 +/- 4%, and 28 +/- 3% at increasing doses of the Nal-Glu antagonist and 12 +/- 4%, 27 +/- 4%, and 30 +/- 7% with increasing doses of the Nal-Arg antagonist. For the Nal-Glu antagonist, suppression of LH was greater than that of FSH and free alpha-subunit at all doses (P less than 0.001), while FSH suppression was greater than that of free alpha-subunit at the highest dose only (P less than 0.05). For the Nal-Arg antagonist, LH suppression was greater than that of FSH or free alpha-subunit at all doses (P greater than 0.01), and FSH suppression exceeded that of free alpha-subunit at the 50 micrograms/kg dose. Suppression of LH was greater with the Nal-Glu antagonist than with the Nal-Arg antagonist at doses of 50 and 150 micrograms/kg (P less than 0.05), and FSH suppression was greater with the Nal-Glu antagonist at 150 micrograms/kg (P less than 0.01), while the degrees of maximum suppression were similar for the two different GnRH antagonists for free alpha-subunit.(ABSTRACT TRUNCATED AT 400 WORDS)
为研究促性腺激素释放激素(GnRH)对促性腺细胞分泌糖蛋白激素的差异调节作用,在月经周期的卵泡早期(第1 - 5天),对甲状腺功能正常的女性给予Nal - Glu GnRH拮抗剂,并将结果与先前使用Nal - Arg GnRH拮抗剂的研究进行比较。在以每10分钟一次的频率进行4小时基线采样后,给每位受试者皮下注射单次剂量的GnRH拮抗剂。频繁采样持续8小时,随后每小时采样再持续16小时。采用高特异性检测方法连续测定促黄体生成素(LH)、促卵泡生成素(FSH)和游离α亚基。在基线采样期间,LH和游离α亚基脉冲的一致性为90%。在最高剂量的Nal - Glu拮抗剂作用下,LH和游离α亚基的脉冲式分泌立即被抑制至少8小时。给予Nal - Glu GnRH拮抗剂后,LH的最大抑制百分比在15、50和150微克/千克剂量时分别为70±4%、80±4%和83±*1%,而给予Nal - Arg GnRH拮抗剂在50、150和500微克/千克剂量时分别为51±10%、70±5%和69±5%。随着Nal - Glu拮抗剂剂量增加,FSH降低幅度分别为28±2%、32±7%和39±2%,而随着Nal - Arg拮抗剂剂量增加,FSH降低幅度分别为25±6%、17±6%和28±4%。随着Nal - Glu拮抗剂剂量增加,游离α亚基降低22±4%、23±4%和28±3%,随着Nal - Arg拮抗剂剂量增加,游离α亚基降低12±4%、27±4%和30±7%。对于Nal - Glu拮抗剂,在所有剂量下LH的抑制均大于FSH和游离α亚基(P<0.001),而仅在最高剂量时FSH的抑制大于游离α亚基(P<0.05)。对于Nal - Arg拮抗剂,在所有剂量下LH的抑制均大于FSH或游离α亚基(P>0.01),在50微克/千克剂量时FSH的抑制超过游离α亚基。在50和150微克/千克剂量时,Nal - Glu拮抗剂对LH的抑制大于Nal - Arg拮抗剂(P<0.05),在150微克/千克剂量时,Nal - Glu拮抗剂对FSH的抑制更大(P<0.01),而两种不同GnRH拮抗剂对游离α亚基的最大抑制程度相似。(摘要截取自400字)