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Gonadotropin secretion in eugonadotropic human males and postmenopausal females under long-term application of a potent analog of gonadotropin-releasing hormone.

作者信息

Happ J, Scholz P, Weber T, Cordes U, Schramm P, Neubauer M, Beyer J

出版信息

Fertil Steril. 1978 Dec;30(6):674-8. doi: 10.1016/s0015-0282(16)43695-2.

DOI:10.1016/s0015-0282(16)43695-2
PMID:365599
Abstract
摘要

相似文献

1
Gonadotropin secretion in eugonadotropic human males and postmenopausal females under long-term application of a potent analog of gonadotropin-releasing hormone.长期应用促性腺激素释放激素强效类似物时，正常促性腺激素分泌的男性和绝经后女性的促性腺激素分泌情况。
Fertil Steril. 1978 Dec;30(6):674-8. doi: 10.1016/s0015-0282(16)43695-2.
2
Gonadotropin and testosterone secretion in normal human males after stimulation with gonadotropin-releasing hormone (GnRH) or potent GnRH analogs using different modes of application.使用不同给药方式，用促性腺激素释放激素（GnRH）或强效GnRH类似物刺激后，正常男性体内促性腺激素和睾酮的分泌情况。
Fertil Steril. 1978 Dec;30(6):666-73. doi: 10.1016/s0015-0282(16)43694-0.
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Concordant suppression of serum immunoreactive luteinizing hormone (LH), follicle-stimulating hormone, alpha subunit, bioactive LH, and testosterone in postmenopausal women by a potent gonadotropin releasing hormone antagonist (detirelix).一种强效促性腺激素释放激素拮抗剂（地瑞瑞克）对绝经后妇女血清免疫反应性促黄体生成素（LH）、促卵泡生成素、α亚基、生物活性LH及睾酮的协同抑制作用
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Short term administration of gonadotropin-releasing hormone analog to a patient with a testosterone-secreting ovarian tumor.
J Clin Endocrinol Metab. 1987 Jun;64(6):1320-2. doi: 10.1210/jcem-64-6-1320.
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Prolonged elevation of luteinizing hormone (LH) after intranasal administration of an analog of LH-releasing hormone.鼻内给予促黄体生成激素释放激素类似物后促黄体生成激素（LH）的长期升高。
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Reduced gonadotropin secretion in postmenopausal women during treatment with a stimulatory LRH analogue.绝经后女性在使用促性腺激素释放激素（LRH）类似物进行刺激治疗期间促性腺激素分泌减少。
J Clin Endocrinol Metab. 1979 Sep;49(3):472-4. doi: 10.1210/jcem-49-3-472.
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Synthetic LH-releasing hormone (LH-RH) administered to normal men by different routes.通过不同途径向正常男性施用合成促黄体生成激素释放激素（LH-RH）。
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Gonadotropins and estradiol responses to single intranasal or subcutaneous administration of a luteinizing hormone-releasing hormone agonist in the early follicular phase.卵泡早期单次经鼻或皮下注射促黄体生成素释放激素激动剂后促性腺激素和雌二醇的反应
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Single subcutaneous doses of a luteinizing hormone-releasing hormone antagonist suppress serum gonadotropin and testosterone levels in normal men.单次皮下注射促黄体生成素释放激素拮抗剂可抑制正常男性的血清促性腺激素和睾酮水平。
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Suppressive actions of a gonadotropin-releasing hormone antagonist on luteinizing hormone, follicle-stimulating hormone, and prolactin release in estrogen-deficient postmenopausal women.促性腺激素释放激素拮抗剂对雌激素缺乏的绝经后妇女黄体生成素、卵泡刺激素和催乳素释放的抑制作用。
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引用本文的文献

1
An oriented phase-II trial of D-Trp6-LH-RH in patients with prostatic carcinoma.
Med Oncol Tumor Pharmacother. 1984;1(2):119-22. doi: 10.1007/BF02934983.
2
Inhibition of the growth of some hormone dependent tumors by D-Trp6-LH-RH.D-色氨酸6-促黄体激素释放激素对某些激素依赖性肿瘤生长的抑制作用。
Med Oncol Tumor Pharmacother. 1984;1(2):109-18. doi: 10.1007/BF02934982.