• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Suppression of ovarian activity by Zoladex depot (ICI 118630), a long-acting luteinizing hormone releasing hormone agonist analogue.

作者信息

West C P, Baird D T

机构信息

Department of Obstetrics and Gynaecology, University of Edinburgh.

出版信息

Clin Endocrinol (Oxf). 1987 Feb;26(2):213-20. doi: 10.1111/j.1365-2265.1987.tb00779.x.

DOI:10.1111/j.1365-2265.1987.tb00779.x
PMID:2959405
Abstract

A long-acting LHRH agonist, Zoladex depot 3.6 mg, was administered as a monthly s.c. injection to seven premenopausal volunteers for a maximum of 6 months, starting in the luteal phase of the cycle. Transient stimulation of gonadotrophin release was observed 24 h after the initial depot, followed by sustained suppression of plasma LH, while FSH levels returned to the normal range. Plasma oestradiol concentrations fell to early follicular phase values within 14 d. Twice-weekly monitoring of urinary oestrone-3-glucuronide and pregnanediol demonstrated inhibition of ovulation and almost complete suppression of ovarian follicular activity throughout therapy. All the subjects became amenorrhoeic. Mean plasma testosterone concentrations were also significantly reduced while androstenedione remained within the pretreatment range. SHBG concentrations were not significantly reduced. After cessation of therapy, postovulatory menstruation occurred within 80 d of administration of the last depot.

摘要

相似文献

1
Suppression of ovarian activity by Zoladex depot (ICI 118630), a long-acting luteinizing hormone releasing hormone agonist analogue.
Clin Endocrinol (Oxf). 1987 Feb;26(2):213-20. doi: 10.1111/j.1365-2265.1987.tb00779.x.
2
Endocrinologic and clinical evaluation following a single administration of a gonadotrophin-releasing hormone agonist (Zoladex), in a depot formulation, to premenopausal women.
Fertil Steril. 1988 Jan;49(1):163-5. doi: 10.1016/s0015-0282(16)59670-8.
3
Suppression of gonadotrophin secretion does not reverse premature ovarian failure.抑制促性腺激素分泌并不能逆转卵巢早衰。
Br J Obstet Gynaecol. 1989 Feb;96(2):196-9. doi: 10.1111/j.1471-0528.1989.tb01662.x.
4
Contraception with an LHRH agonist: effect on gonadotrophin and steroid secretion patterns.使用促黄体生成素释放激素(LHRH)激动剂避孕:对促性腺激素和类固醇分泌模式的影响。
Clin Endocrinol (Oxf). 1984 Aug;21(2):179-88. doi: 10.1111/j.1365-2265.1984.tb03458.x.
5
Inhibition of ovulation during discontinuous intranasal luteinizing hormone-releasing hormone agonist dosing in combination with gestagen-induced bleeding.在间断经鼻给予促黄体生成素释放激素激动剂并联合孕激素诱导出血期间对排卵的抑制作用。
Fertil Steril. 1985 Jun;43(6):868-77. doi: 10.1016/s0015-0282(16)48614-0.
6
Treatment of a patient with severe menstrual migraine using the depot LHRH analogue Zoladex.使用长效促性腺激素释放激素(LHRH)类似物诺雷德治疗重度月经性偏头痛患者。
Aust N Z J Obstet Gynaecol. 1991 May;31(2):164-5. doi: 10.1111/j.1479-828x.1991.tb01808.x.
7
Preliminary endocrinological evaluation of a sustained-release formulation of the LH-releasing hormone agonist D-Ser(But)6Azgly10LHRH in premenopausal women with advanced breast cancer.
J Endocrinol. 1986 Nov;111(2):349-53. doi: 10.1677/joe.0.1110349.
8
Prolactin and pituitary gonadotropin values and responses to acute luteinizing hormone-releasing hormone (LHRH) challenge in patients having long-term treatment with a depot LHRH analogue.长期接受长效促黄体生成素释放激素(LHRH)类似物治疗的患者的催乳素和垂体促性腺激素值以及对急性LHRH激发试验的反应。
Cancer. 1991 Feb 1;67(3):557-9. doi: 10.1002/1097-0142(19910201)67:3<557::aid-cncr2820670304>3.0.co;2-c.
9
Long-acting gonadotrophin releasing hormone agonist implant causes variable duration of suppression of ovarian steroid and inhibin secretion.长效促性腺激素释放激素激动剂植入物导致卵巢甾体激素和抑制素分泌抑制的持续时间存在差异。
Clin Endocrinol (Oxf). 1992 Jan;36(1):97-104. doi: 10.1111/j.1365-2265.1992.tb02908.x.
10
Comparison of mammalian luteinizing hormone releasing hormone (LH-RH), and of an analog (ICI 118630), on luteinizing hormone and ovarian steroid (progesterone, oestradiol) secretions in laying hens. (Gallus domesticus).
Life Sci. 1986 Aug 11;39(6):541-7. doi: 10.1016/0024-3205(86)90511-4.

引用本文的文献

1
Nocturnal Hot Flashes: Relationship to Objective Awakenings and Sleep Stage Transitions.夜间潮热:与客观觉醒及睡眠阶段转换的关系
J Clin Sleep Med. 2016 Jul 15;12(7):1003-9. doi: 10.5664/jcsm.5936.
2
A gonadotropin-releasing hormone agonist model demonstrates that nocturnal hot flashes interrupt objective sleep.促性腺激素释放激素激动剂模型表明,夜间潮热会干扰客观睡眠。
Sleep. 2013 Dec 1;36(12):1977-85. doi: 10.5665/sleep.3244.
3
Adverse effects of induced hot flashes on objectively recorded and subjectively reported sleep: results of a gonadotropin-releasing hormone agonist experimental protocol.
诱导性热潮红对客观记录和主观报告的睡眠的不良影响:促性腺激素释放激素激动剂实验方案的结果。
Menopause. 2013 Sep;20(9):905-14. doi: 10.1097/GME.0b013e31828292d1.
4
Two different formulations with equivalent effect? Comparison of serum estradiol suppression with monthly goserelin and trimonthly leuprolide in breast cancer patients.两种等效作用的不同配方?每月戈舍瑞林和每三月亮丙瑞林在乳腺癌患者中抑制血清雌二醇的比较。
Med Oncol. 2013 Mar;30(1):354. doi: 10.1007/s12032-012-0354-1. Epub 2012 Dec 29.
5
Goserelin: a review of its use in the treatment of early breast cancer in premenopausal and perimenopausal women.戈舍瑞林:用于治疗绝经前和围绝经期妇女早期乳腺癌的综述
Drugs. 2005;65(18):2639-55. doi: 10.2165/00003495-200565180-00011.
6
Current drug therapy recommendations for the treatment of endometriosis.
Drugs. 1999 Jul;58(1):39-50. doi: 10.2165/00003495-199958010-00004.
7
Luteinizing hormone-releasing hormone analogues--the rationale for adjuvant use in premenopausal women with early breast cancer.促黄体生成激素释放激素类似物——绝经前早期乳腺癌女性辅助治疗的理论依据。
Br J Cancer. 1998 Sep;78 Suppl 4(Suppl 4):5-8. doi: 10.1038/bjc.1998.754.
8
Goserelin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in benign gynaecological disorders.戈舍瑞林。对其药效学和药代动力学特性以及在良性妇科疾病中的治疗应用的综述。
Drugs. 1996 Feb;51(2):319-46. doi: 10.2165/00003495-199651020-00009.
9
Goserelin. A review of its pharmacodynamic and pharmacokinetic properties, and clinical use in sex hormone-related conditions.戈舍瑞林。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应用的综述。
Drugs. 1991 Feb;41(2):254-88. doi: 10.2165/00003495-199141020-00008.