Extra-pituitary inhibition of testicular function by luteinising hormone releasing hormone.

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超能文献

作者信息

Hsueh A J, Erickson G F

出版信息

Nature. 1979 Sep 6;281(5726):66-7. doi: 10.1038/281066a0.

DOI:10.1038/281066a0

PMID:233123

Abstract

摘要

相似文献

Extra-pituitary inhibition of testicular function by luteinising hormone releasing hormone.

Nature. 1979 Sep 6;281(5726):66-7. doi: 10.1038/281066a0.

Androgen biosynthesis in Leydig cells after testicular desensitization by luteinizing hormone-releasing hormone and human chorionic gonadotropin.

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Gonadotropin-releasing hormone and its agonist inhibit testicular luteinizing hormone receptor and steroidogenesis in immature and adult hypophysectomized rats.促性腺激素释放激素及其激动剂抑制未成熟和成年去垂体大鼠睾丸中的促黄体生成素受体及类固醇生成。

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Luteinizing hormone-releasing hormone-induced regulation of gonadotropin and prolactin receptors in the rat testis.促黄体生成素释放激素对大鼠睾丸中促性腺激素和催乳素受体的诱导调节作用。

Endocrinology. 1979 Jan;104(1):17-25. doi: 10.1210/endo-104-1-17.

Reduction of testicular luteinizing hormone/human chorionic gonadotropin receptors by [D-Trp6]-luteinizing hormone releasing hormone in hypophysectomized rats.

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Antifertility effects of LHRH agonists in the male rat and inhibition of testicular steroidogenesis in man.促黄体生成素释放激素（LHRH）激动剂对雄性大鼠的抗生育作用及对人体睾丸类固醇生成的抑制作用。

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Direct inhibitory effect of gonadotropin-releasing hormone upon follicle-stimulating hormone induction of luteinizing hormone receptor and aromatase activity in rat granulosa cells.

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Direct inhibition of testicular function by gonadotropin-releasing hormone: mediation by specific gonadotropin-releasing hormone receptors in interstitial cells.促性腺激素释放激素对睾丸功能的直接抑制：间质细胞中特定促性腺激素释放激素受体的介导作用

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Modulation of prolactin, luteinizing hormone (LH) and follicle stimulating hormone (FSH) secretion by LHRH and bromocriptine (CB154) in the hypophysectomized pituitary-grafted male rat and its effect on testicular LH receptors and testosterone output.促性腺激素释放激素（LHRH）和溴隐亭（CB154）对垂体切除并移植垂体的雄性大鼠催乳素、黄体生成素（LH）和卵泡刺激素（FSH）分泌的调节及其对睾丸LH受体和睾酮分泌的影响。

Biol Reprod. 1979 Aug;21(1):141-7. doi: 10.1095/biolreprod21.1.141.

Inhibition of testicular luteinizing hormone receptor level by treatment with a potent luteinizing hormone-releasing hormone agonist of human chorionic gonadotropin.

Biochem Biophys Res Commun. 1977 Jun 6;76(3):855-62. doi: 10.1016/0006-291x(77)91579-0.

引用本文的文献

Expression and Role of Gonadotropin-Releasing Hormone 2 and Its Receptor in Mammals.促性腺激素释放激素2及其受体在哺乳动物中的表达与作用

Front Endocrinol (Lausanne). 2017 Dec 11;8:269. doi: 10.3389/fendo.2017.00269. eCollection 2017.

Neuropeptides in the gonads: from evolution to pharmacology.性腺中的神经肽：从进化到药理学

Front Pharmacol. 2010 Sep 9;1:114. doi: 10.3389/fphar.2010.00114. eCollection 2010.

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.

Tumor growth inhibition in patients with prostatic carcinoma treated with luteinizing hormone-releasing hormone agonists.用促黄体生成素释放激素激动剂治疗的前列腺癌患者的肿瘤生长抑制

Proc Natl Acad Sci U S A. 1982 Mar;79(5):1658-62. doi: 10.1073/pnas.79.5.1658.

Suppression of androgen production by D-tryptophan-6-luteinizing hormone-releasing hormone in man.D-色氨酸-6-促黄体生成素释放激素对男性雄激素生成的抑制作用。

J Clin Invest. 1981 Sep;68(3):819-22. doi: 10.1172/jci110320.

Progress in neuroendocrinology: LH releasing (LHRH), basic and clinical aspects.神经内分泌学进展：促黄体生成素释放激素（LHRH），基础与临床方面

J Endocrinol Invest. 1983 Jun;6(3):243-51. doi: 10.1007/BF03350615.

Proc Natl Acad Sci U S A. 1980 Aug;77(8):4459-63. doi: 10.1073/pnas.77.8.4459.

Estrogen dependence of a gonadotropin-induced steroidogenic lesion in rat testicular Leydig cells.大鼠睾丸间质细胞中促性腺激素诱导的类固醇生成损伤的雌激素依赖性。

J Clin Invest. 1980 Mar;65(3):699-705. doi: 10.1172/JCI109716.

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.

Effects of a potent LHRH-agonist on the pituitary gonadal axis with and without testosterone substitution.

Urol Res. 1986;14(5):261-4. doi: 10.1007/BF00256570.

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