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通过促性腺激素释放激素超级激动剂那法瑞林抑制排卵实现鼻内肽类避孕:六个月临床结果

Intranasal peptide contraception by inhibition of ovulation with the gonadotropin-releasing hormone superagonist nafarelin: six months' clinical results.

作者信息

Gudmundsson J A, Nillius S J, Bergquist C

出版信息

Fertil Steril. 1986 May;45(5):617-23. doi: 10.1016/s0015-0282(16)49331-3.

DOI:10.1016/s0015-0282(16)49331-3
PMID:2938984
Abstract

Forty-seven woman volunteers used a new highly potent stimulatory analog of the hypothalamic gonadotropin-releasing hormone (GnRH) for contraception. The superagonist nafarelin acetate, D-Nal(2)6-GnRH, was administered intranasally in one daily dose of 125 micrograms to 25 women and 250 micrograms to 22 women. Ovulation was consistently inhibited during 261 of 262 treatment months. No pregnancy occurred during 222 months in which no additional contraceptives were used. The mean plasma estradiol level after 6 months of treatment was 162 pmol/l. The predominant bleeding pattern was oligomenorrhea. Three women on the lower dose and six women on the higher dose discontinued the trial prematurely, mainly because of hot flushes. No serious side effects were reported. Ovulatory menstruations returned after a median time of 43 days after discontinuation of therapy. Daily intranasal nafarelin treatment for inhibition of ovulation proved to be an effective and rapidly reversible method of contraception.

摘要

47名女性志愿者使用了一种新型的、高效的下丘脑促性腺激素释放激素(GnRH)刺激类似物进行避孕。超激动剂醋酸那法瑞林,即D-Nal(2)6-GnRH,以每日一次的剂量经鼻给药,25名女性的剂量为125微克,22名女性的剂量为250微克。在262个治疗月中的261个月里,排卵持续受到抑制。在222个月未使用其他避孕措施的期间内未发生妊娠。治疗6个月后的平均血浆雌二醇水平为162 pmol/l。主要的出血模式为月经过少。3名低剂量组女性和6名高剂量组女性提前终止了试验,主要原因是潮热。未报告严重副作用。停药后排卵性月经恢复的中位时间为43天。每日经鼻给予那法瑞林以抑制排卵被证明是一种有效且可逆性快速的避孕方法。

相似文献

1
Intranasal peptide contraception by inhibition of ovulation with the gonadotropin-releasing hormone superagonist nafarelin: six months' clinical results.通过促性腺激素释放激素超级激动剂那法瑞林抑制排卵实现鼻内肽类避孕:六个月临床结果
Fertil Steril. 1986 May;45(5):617-23. doi: 10.1016/s0015-0282(16)49331-3.
2
Inhibition of ovulation by intranasal nafarelin, a new superactive agonist of GnRH.
Contraception. 1984 Aug;30(2):107-14. doi: 10.1016/0010-7824(84)90094-5.
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Ovulation inhibition with nafarelin acetate nasal administration for six months.使用醋酸那法瑞林经鼻给药抑制排卵六个月。
Contraception. 1985 Dec;32(6):531-51. doi: 10.1016/s0010-7824(85)80001-9.
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Gonadotropin releasing hormone analogs for female contraception by inhibition of ovulation.通过抑制排卵实现女性避孕的促性腺激素释放激素类似物。
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Peptide contraception by inhibition of ovulation with intranasal GnRH superagonist: clinical and metabolic aspects.通过鼻内给予促性腺激素释放激素(GnRH)超激动剂抑制排卵实现肽类避孕:临床及代谢方面
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A new superagonist of GnRH for inhibition of ovulation in women.一种用于抑制女性排卵的新型促性腺激素释放激素(GnRH)超激动剂。
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Dose-dependent inhibition of pituitary-ovarian function during administration of a gonadotropin-releasing hormone agonistic analog (nafarelin).促性腺激素释放激素激动剂类似物(那法瑞林)给药期间垂体-卵巢功能的剂量依赖性抑制
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Endometrial patterns in women on chronic luteinizing hormone-releasing hormone agonist treatment for contraception.接受慢性促黄体生成素释放激素激动剂治疗以避孕的女性的子宫内膜模式。
Fertil Steril. 1981 Sep;36(3):339-42. doi: 10.1016/s0015-0282(16)45735-3.

引用本文的文献

1
Clinical applications of GnRH analogs.促性腺激素释放激素类似物的临床应用。
J Endocrinol Invest. 1988 Nov;11(10):745-54. doi: 10.1007/BF03350939.
2
LHRH agonists and the prevention of breast and ovarian cancer.促黄体生成素释放激素激动剂与乳腺癌和卵巢癌的预防
Br J Cancer. 1989 Jul;60(1):142-8. doi: 10.1038/bjc.1989.237.
3
Nafarelin. A review of its pharmacodynamic and pharmacokinetic properties, and clinical potential in sex hormone-related conditions.那法瑞林。对其药效学和药代动力学特性以及在性激素相关病症中的临床潜力的综述。
Drugs. 1990 Apr;39(4):523-51. doi: 10.2165/00003495-199039040-00005.