Department of Investigative Medicine, Imperial College London, Sixth Floor, Commonwealth Building, Hammersmith Hospital, Du Cane Road, London W12 ONN, United Kingdom.
J Clin Endocrinol Metab. 2013 Nov;98(11):4464-74. doi: 10.1210/jc.2013-1069. Epub 2013 Sep 12.
Kisspeptin is a critical hypothalamic regulator of reproductive function. Chronic kisspeptin administration causes profound tachyphylaxis in male monkeys and in women with functional hypothalamic amenorrhea. The pharmacological effects of chronic kisspeptin exposure in healthy women with normal menstrual cycles have not been studied previously.
Our aim was to determine the effects of follicular-phase kisspeptin-54 treatment on menstrual cyclicity in healthy women.
We performed a prospective, single-blinded, 1-way crossover study. Healthy women received twice-daily sc injections of kisspeptin (6.4 nmol/kg) or 0.9% saline during menstrual days 7-14 (n = 5 per treatment arm). Serial assessments of basal reproductive hormones, ultrasound parameters, LH pulsatility, and acute sensitivity to GnRH and kisspeptin-54 injection were performed.
Menstrual cyclicity persisted in all women after follicular-phase kisspeptin-54 treatment. Chronic exposure to kisspeptin-54 did not abolish acute stimulation of LH after injection of kisspeptin-54 or GnRH. In addition, kisspeptin-54 treatment was associated with a shorter mean length of the menstrual cycle (mean length of menstrual cycle was 28.6 ± 1.4 days with saline vs 26.8 ± 3.1 days with kisspeptin, P < .01), earlier onset of highest recorded serum LH (mean menstrual day of highest LH was 15.2 ± 1.3 with saline vs 13.0 ± 1.9 with kisspeptin, P < .05), and earlier onset of the luteal phase (mean menstrual day of progesterone increase was 18.0 ± 2.1 with saline vs 15.8 ± 0.9 with kisspeptin, P < .05).
Our data suggest that 1 week of exogenous kisspeptin-54 does not abolish menstrual cyclicity in healthy women. Further work is needed to determine whether kisspeptin could be used to treat certain anovulatory disorders.
kisspeptin 是调节生殖功能的关键下丘脑调节剂。慢性 kisspeptin 给药会导致雄性猴子和功能性下丘脑闭经的女性出现明显的脱敏作用。以前尚未研究过正常月经周期的健康女性中慢性 kisspeptin 暴露的药理学作用。
本研究旨在确定卵泡期 kisspeptin-54 治疗对健康女性月经周期的影响。
我们进行了一项前瞻性、单盲、1 向交叉研究。健康女性在月经第 7-14 天(每组 5 人)接受每日两次皮下注射 kisspeptin(6.4 nmol/kg)或 0.9%生理盐水。进行了基础生殖激素、超声参数、LH 脉冲性、以及 GnRH 和 kisspeptin-54 注射的急性敏感性的连续评估。
所有女性在卵泡期 kisspeptin-54 治疗后月经周期仍持续。慢性 kisspeptin-54 暴露不会消除 kisspeptin-54 或 GnRH 注射后 LH 的急性刺激。此外,kisspeptin-54 治疗与月经周期的平均长度缩短有关(生理盐水组的平均月经周期长度为 28.6±1.4 天,kisspeptin 组为 26.8±3.1 天,P<.01),最高记录血清 LH 的出现时间更早(生理盐水组的最高 LH 月经日为 15.2±1.3,kisspeptin 组为 13.0±1.9,P<.05),黄体期出现时间更早(孕激素升高的平均月经日为 18.0±2.1,生理盐水组为 15.8±0.9,kisspeptin 组为 15.8±0.9,P<.05)。
我们的数据表明,1 周的外源性 kisspeptin-54 不会破坏健康女性的月经周期。需要进一步研究以确定 kisspeptin 是否可用于治疗某些排卵障碍。