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Ovarian growth and uptake of iodinated D-leu, des Gly NH2 -LHRH ethylamide in HCG treated rats.

作者信息

Mayar M Q, Tarnavsky G K, Reeves J J

出版信息

Proc Soc Exp Biol Med. 1979 Jun;161(2):216-9. doi: 10.3181/00379727-161-40523.

DOI:10.3181/00379727-161-40523
PMID:377298
Abstract
摘要

相似文献

1
Ovarian growth and uptake of iodinated D-leu, des Gly NH2 -LHRH ethylamide in HCG treated rats.人绒毛膜促性腺激素处理的大鼠中卵巢对碘化D-亮氨酸、去甘氨酰胺-LHRH乙酰胺的摄取及卵巢生长情况
Proc Soc Exp Biol Med. 1979 Jun;161(2):216-9. doi: 10.3181/00379727-161-40523.
2
Inhibitory effects of long term treatment with a luteinizing hormone-releasing hormone agonist on the pituitary-gonadal axis in male and female rats.促黄体生成素释放激素激动剂长期治疗对雄性和雌性大鼠垂体-性腺轴的抑制作用。
Endocrinology. 1979 May;104(5):1369-76. doi: 10.1210/endo-104-5-1369.
3
Inhibition of ovarian luteinizing hormone (LH) and follicle-stimulating hormone receptor levels with an LH-releasing hormone agonist during the estrous cycle in the rat.在大鼠发情周期中，使用促黄体生成素释放激素激动剂抑制卵巢促黄体生成素（LH）和促卵泡激素受体水平。
Fertil Steril. 1978 Sep;30(3):348-53. doi: 10.1016/s0015-0282(16)43524-7.
4
Inhibition of endopeptidase 24.15 greatly increases the release of luteinizing hormone and follicle stimulating hormone in response to luteinizing hormone/releasing hormone.抑制内肽酶24.15可显著增加促黄体激素和促卵泡激素对促黄体激素释放激素的反应性释放。
J Pharmacol Exp Ther. 1990 Jun;253(3):1265-71.
5
Relative activity, plasma elimination and tissue degradation of synthetic luteinizing hormone releasing hormone and certain of its analogues.合成促黄体生成激素释放激素及其某些类似物的相对活性、血浆消除和组织降解
J Endocrinol. 1979 Jan;80(1):141-52. doi: 10.1677/joe.0.0800141.
6
Distribution of luteinizing hormone-releasing hormone receptors in the rat ovary.
Regul Pept. 1982 Sep;4(4):183-90. doi: 10.1016/0167-0115(82)90110-0.
7
Unusual anti-reproductive properties of the analog [d-Leu6,des-Gly-NH2(10)]-luteinizing hormone-releasing hormone ethylamide in male rats.类似物[D-亮氨酸6，去甘氨酰胺（10）]-促黄体生成激素释放激素乙酰胺在雄性大鼠中的异常抗生殖特性。
Fertil Steril. 1978 Nov;30(5):600-3.
8
Uptake of iodinated luteinizing hormone releasing hormone analogs in the pituitary.
Endocrinology. 1977 Aug;101(2):540-7. doi: 10.1210/endo-101-2-540.
9
Pituitary responsiveness following infusion or repeated injections of [D-Leu6, des Gly-NH210]-LHRH-ethylamide in prepubertal ewes.青春期前母羊输注或重复注射[D-亮氨酸6，去甘氨酰胺10]-LHRH-乙酰胺后的垂体反应性。
J Anim Sci. 1978 Jul;47(1):235-40. doi: 10.2527/jas1978.471235x.
10
Multiple inhibitory effects of a luteinizing hormone-releasing hormone agonist on hCG-dependent steroidogenesis and on FSH-dependent responses in ovarian cells in vivo and in vitro.促黄体生成素释放激素激动剂对体内外卵巢细胞中依赖人绒毛膜促性腺激素的类固醇生成及依赖促卵泡生成素的反应的多种抑制作用。
Endocrinol Jpn. 1982 Oct;29(5):597-605. doi: 10.1507/endocrj1954.29.597.

引用本文的文献

1
Effect of chronic treatment with [D-Ala6, des-Gly-NH210]LHRH ethylamide on ovarian histology in the rat.[D-丙氨酸6，去甘氨酰胺10]促黄体激素释放激素乙酰胺长期治疗对大鼠卵巢组织学的影响。
Cell Tissue Res. 1982;227(1):213-9. doi: 10.1007/BF00206342.
2
Similar luteinizing hormone-releasing hormone binding sites in rat anterior pituitary and ovary.大鼠垂体前叶和卵巢中类似的促黄体生成激素释放激素结合位点。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5567-71. doi: 10.1073/pnas.77.9.5567.