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Biological activity of surfagon--a synthetic luliberin agonist.

作者信息

Krivosheev O G, Nabatchikova N A, Pozdnyakova G I, Syutkin E A, Vinogradov V A, Veselova S P, Saks T R, Meertsuk F E

机构信息

All-Union Cardiologic Science Center, Academy of Medical Sciences of the USSR, Moscow.

出版信息

Neurosci Behav Physiol. 1989 Jul-Aug;19(4):341-5. doi: 10.1007/BF01236026.

DOI:10.1007/BF01236026
PMID:2510052
Abstract
摘要

相似文献

1
Biological activity of surfagon--a synthetic luliberin agonist.促排素的生物活性——一种合成的促黄体素释放激素激动剂
Neurosci Behav Physiol. 1989 Jul-Aug;19(4):341-5. doi: 10.1007/BF01236026.
2
[Biological activity of surfagon--a synthetic luliberin agonist].[促排素的生物活性——一种合成的促黄体素释放激素激动剂]
Probl Endokrinol (Mosk). 1988 Nov-Dec;34(6):62-6.
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Prolonged release by dioestrous rats of follicle-stimulating hormone during the period of ovulation induced by luteinizing hormone releasing hormone.
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Synthetic analogs of luteinizing hormone releasing hormone (LH-RH) substituted in position 6 and 10.在第6位和第10位被取代的促黄体生成素释放激素（LH-RH）的合成类似物。
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Effects of ovariectomy and steroid treatment on hypophyseal sensitivity to purified LH-releasing factor (LRF).卵巢切除术和类固醇治疗对垂体对纯化促黄体生成素释放因子（LRF）敏感性的影响。
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Further studies on the structure-activity relationships in the C-terminal part of luteinizing hormone-releasing hormone.
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Decreased pituitary responsiveness and inhibition of the luteinizing hormone surge and ovulation in the stumptailed monkey (Macaca arctoides) by chronic treatment with an agonist of luteinizing hormone-releasing hormone.通过长期使用促黄体生成素释放激素激动剂治疗，断尾猴（熊猴）垂体反应性降低，促黄体生成素高峰及排卵受到抑制。
Endocrinology. 1980 Feb;106(2):452-7. doi: 10.1210/endo-106-2-452.
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Presence of proline in position 3 for potent inhibition of the activity of the luteinizing hormone releasing hormone and of ovulation.脯氨酸位于第3位可有效抑制促黄体生成素释放激素的活性及排卵。
Biochem Biophys Res Commun. 1976 Oct 4;72(3):939-44. doi: 10.1016/s0006-291x(76)80222-7.
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Changes in the sensitivity of the pituitary gland to luteinizing hormone releasing factor during the oestrous cycle of the rat.大鼠发情周期中垂体对促黄体生成素释放因子敏感性的变化。
J Endocrinol. 1974 Jan;60(1):47-64. doi: 10.1677/joe.0.0600047.

本文引用的文献

1
Plasma luteinizing hormone response to increasing doses of synthetic gonadotrophin-releasing hormone in heifers.小母牛对递增剂量合成促性腺激素释放激素的血浆促黄体生成素反应
Acta Vet Scand. 1983;24(2):211-24. doi: 10.1186/BF03546748.
2
Pituitary binding and internalization of radioiodinated gonadotropin-releasing hormone agonist and antagonist ligands in vitro and in vivo.放射性碘标记的促性腺激素释放激素激动剂和拮抗剂配体在体外和体内的垂体结合及内化作用
Endocrinology. 1986 Oct;119(4):1852-63. doi: 10.1210/endo-119-4-1852.
3
LHRH, the role of LHRH (agonists) in the regulation of gonadal function.
促性腺激素释放激素，促性腺激素释放激素（激动剂）在性腺功能调节中的作用。
Acta Endocrinol Suppl (Copenh). 1986;276:76-84. doi: 10.1530/acta.0.111s0076.
4
Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: rationale and perspective.促性腺激素释放激素类似物设计。激动剂和拮抗剂开发的结构-功能研究：原理与展望。
Endocr Rev. 1986 Feb;7(1):44-66. doi: 10.1210/edrv-7-1-44.