年轻正常成年男性中促黄体生成素和性腺类固醇对单次鼻内给予促性腺激素释放激素激动剂（Hoe-766）反应的敏感性 - Suppr

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超能文献

Sensitivity of luteinizing hormone and gonadal steroid responses to single intranasal administration of an LHRH agonist (Hoe-766) in young normal adult men.

作者信息

Faure N, Labrie F, Belanger A, Lemay A, Raynaud J P, Von der Ohe M, Fazekas A T

出版信息

J Endocrinol Invest. 1982 Nov-Dec;5(6):355-60. doi: 10.1007/BF03350532.

DOI:10.1007/BF03350532

PMID:6820372

Abstract

摘要

相似文献

Sensitivity of luteinizing hormone and gonadal steroid responses to single intranasal administration of an LHRH agonist (Hoe-766) in young normal adult men.年轻正常成年男性中促黄体生成素和性腺类固醇对单次鼻内给予促性腺激素释放激素激动剂（Hoe-766）反应的敏感性

J Endocrinol Invest. 1982 Nov-Dec;5(6):355-60. doi: 10.1007/BF03350532.

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.

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.

Sensitivity of pituitary and corpus luteum responses to single intranasal administration of (D-ser[TBU]6-des-gly-NH2(10)) luteinizing hormone-releasing hormone ethylamide (Buserelin) in normal women.正常女性垂体和黄体对单次鼻内给予（D-丝氨酸[TBU]6-去甘氨酰胺（10））促黄体生成素释放激素乙酰胺（布舍瑞林）反应的敏感性。

Fertil Steril. 1982 Feb;37(2):193-200. doi: 10.1016/s0015-0282(16)46038-3.

Effect of a new LH-RH analogue (D-Ser(TBU)6-EA10-LH-RH) on gonadotrophin and gonadal steroid secretion in men.一种新型促黄体生成激素释放激素类似物（D-丝氨酸（叔丁基）6-EA10-促黄体生成激素释放激素）对男性促性腺激素和性腺类固醇分泌的影响。

Horm Res. 1976;7(1):1-10. doi: 10.1159/000178702.

[Effect of the steroid sex hormones on the LH and FSH responses to LHRH in the normal subject].[类固醇性激素对正常受试者促黄体生成素（LH）和促卵泡生成素（FSH）对促性腺激素释放激素（LHRH）反应的影响]

Pathol Biol (Paris). 1975 Dec;23(10):917-22.

Ovulation inhibition by daily i.m. administration of a highly active LH-RH analog (d-ser(TBU)6-LH-RH-(1-9)-nonapeptide-ethylamide).通过每日肌肉注射一种高活性促黄体生成素释放激素类似物（d-丝氨酸（叔丁基）6-促黄体生成素释放激素-（1-9）-九肽乙酰胺）抑制排卵。

Contraception. 1980 Feb;21(2):191-7. doi: 10.1016/0010-7824(80)90131-6.

Inhibition of serum androgen levels by chronic intranasal and subcutaneous administration of a potent luteinizing hormone-releasing hormone (LH-RH) agonist in adult men.成年男性长期经鼻内和皮下给予强效促黄体生成激素释放激素（LH-RH）激动剂对血清雄激素水平的抑制作用。

Fertil Steril. 1982 Mar;37(3):416-24. doi: 10.1016/s0015-0282(16)46107-8.

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

Fertil Steril. 1983 May;39(5):668-73. doi: 10.1016/s0015-0282(16)47063-9.

Effects of chronic treatment with a potent luteinizing hormone releasing hormone agonist on serum luteinizing hormone and steroid levels in the male rhesus monkey.强效促黄体生成素释放激素激动剂长期治疗对雄性恒河猴血清促黄体生成素和类固醇水平的影响。

Biol Reprod. 1982 Apr;26(3):378-84. doi: 10.1095/biolreprod26.3.378.

引用本文的文献

Buserelin. A review of its pharmacodynamic and pharmacokinetic properties, and clinical profile.布舍瑞林。对其药效学和药代动力学特性以及临床概况的综述。

Drugs. 1990 Mar;39(3):399-437. doi: 10.2165/00003495-199039030-00007.

本文引用的文献

Specific binding of a potent LHRH agonist in rat testis.一种强效促黄体生成素释放激素激动剂在大鼠睾丸中的特异性结合。

Mol Cell Endocrinol. 1980 Nov;20(2):127-34. doi: 10.1016/0303-7207(80)90076-3.

Inhibitory effects of a single intranasal administration of [D-Ser(TBU)6, des-Gly-NH210]LHRH ethylamide, a potent LHRH agonist, on serum steroid levels in normal adult men.强效促性腺激素释放激素（LHRH）激动剂[D-丝氨酸（叔丁基）6，去甘氨酸-NH2 10]LHRH乙酰胺单次鼻内给药对正常成年男性血清类固醇水平的抑制作用。

J Steroid Biochem. 1980 Feb;13(2):123-6. doi: 10.1016/0022-4731(80)90182-x.

Increased testicular 5 alpha-androstane-3 alpha, 17 beta-diol formation induced by treatment with [D-Ser (TBU) 6, des-Gly-NH2(10)] LHRH ethylamide in the rat.[D-丝氨酸（叔丁基）6，去甘氨酰胺（10）]促性腺激素释放激素乙酰胺处理大鼠后诱导睾丸5α-雄甾烷-3α，17β-二醇生成增加。

Steroids. 1980 Oct;36(4):383-91. doi: 10.1016/0039-128x(80)90027-6.

HCG stimulation of testicular LHRH-like activity.人绒毛膜促性腺激素对睾丸促性腺激素释放激素样活性的刺激作用。

Nature. 1980 Oct 16;287(5783):642-3. doi: 10.1038/287642a0.

Testicular GnRH receptors--characterization and localization on interstitial tissue.睾丸促性腺激素释放激素受体——间质组织的特性与定位

J Clin Endocrinol Metab. 1980 Aug;51(2):407-9. doi: 10.1210/jcem-51-2-407.

Time-course of the effect of treatment with a potent LHRH agonist on testicular steroidogenesis and gonadotropin receptor levels in the adult rat.强效促黄体生成素释放激素（LHRH）激动剂治疗对成年大鼠睾丸类固醇生成及促性腺激素受体水平的影响的时间进程。

J Steroid Biochem. 1980 Feb;13(2):191-6. doi: 10.1016/0022-4731(80)90191-0.

Leydig cell receptors for luteinizing hormone releasing hormone and its agonists and their modulation by administration or deprivation of the releasing hormone.黄体生成素释放激素及其激动剂的睾丸间质细胞受体，以及通过给予或剥夺释放激素对其进行的调节。

Biochem Biophys Res Commun. 1980 Jul 16;95(1):256-62. doi: 10.1016/0006-291x(80)90732-9.

Inhibitory effects on gonadotrophin secretion and gonadal function in men during chronic treatment with a potent stimulatory luteinizing hormone-releasing hormone analogue.强效促黄体生成素释放激素类似物长期治疗男性期间对促性腺激素分泌和性腺功能的抑制作用

Acta Endocrinol (Copenh). 1979 Aug;91(4):601-8. doi: 10.1530/acta.0.0910601.

Chronic effects of [D-Trp6,Pro9-NEt]luteinizing hormone-releasing factor on reproductive processes in the male rat.[D-色氨酸6，脯氨酸9-乙酯]促黄体生成素释放因子对雄性大鼠生殖过程的慢性影响。

Endocrinology. 1979 Nov;105(5):1191-201. doi: 10.1210/endo-105-5-1191.

Inhibition of spermatogenesis in the rat by treatment with [D-Ala6, Des-Gly-NH210] LHRH ethylamide.用[D-丙氨酸6，去甘氨酰胺10]促黄体激素释放激素乙酰胺处理对大鼠精子发生的抑制作用。

Endocrinology. 1978 Aug;103(2):641-3. doi: 10.1210/endo-103-2-641.

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