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类固醇与排卵时的卵泡破裂。

Steroids and follicular rupture at ovulation.

作者信息

Tsafriri A, Abisogun A O, Reich R

机构信息

Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.

出版信息

J Steroid Biochem. 1987;27(1-3):359-63. doi: 10.1016/0022-4731(87)90328-1.

DOI:10.1016/0022-4731(87)90328-1
PMID:2961934
Abstract

The preovulatory surge of gonadotropins stimulates follicular steroidogenesis and changes from estrogen as the major product to progesterone. We shall overview the studies dealing with the role of ovarian steroidogenesis in follicular rupture at ovulation. Several inhibitors of steroidogenesis blocked follicular rupture in vivo. Likewise, RU 38486 partially blocked ovulation triggered by hCG. Collectively, these data support the knowledge that follicular steroidogenesis is required for ovulation. Recent studies confirmed the essential role of plasminogen activator (PA) in follicular rupture. The LH stimulation of PA activity was partially blocked by several inhibitors of steroidogenesis and it could be restored by the addition of progesterone, testosterone and estradiol-17 beta, but not the non-aromatizable 5 alpha-dihydrotestosterone. Gonadotropic stimulation enhanced only the synthesis of tissue type PA (t-PA) and not that of urokinase. Likewise, inhibition of steroidogenesis, reduced only the synthesis of t-PA and was reversed by addition of estradiol-17 beta. It seems, therefore, that follicular steroids, most probably estrogen, are involved in the preovulatory rise in follicular t-PA activity.

摘要

促性腺激素的排卵前激增刺激卵泡类固醇生成,并使主要产物从雌激素转变为孕酮。我们将概述有关卵巢类固醇生成在排卵时卵泡破裂中作用的研究。几种类固醇生成抑制剂在体内阻断了卵泡破裂。同样,RU 38486部分阻断了hCG触发的排卵。总体而言,这些数据支持了排卵需要卵泡类固醇生成这一认识。最近的研究证实了纤溶酶原激活物(PA)在卵泡破裂中的重要作用。促黄体生成素(LH)对PA活性的刺激被几种类固醇生成抑制剂部分阻断,并且通过添加孕酮、睾酮和雌二醇-17β可以恢复,但不可芳香化的5α-二氢睾酮则不能。促性腺激素刺激仅增强了组织型PA(t-PA)的合成,而未增强尿激酶的合成。同样,类固醇生成的抑制仅降低了t-PA的合成,并通过添加雌二醇-17β得以逆转。因此,似乎卵泡类固醇,很可能是雌激素,参与了卵泡t-PA活性的排卵前升高。

相似文献

1
Steroids and follicular rupture at ovulation.类固醇与排卵时的卵泡破裂。
J Steroid Biochem. 1987;27(1-3):359-63. doi: 10.1016/0022-4731(87)90328-1.
2
Follicular plasminogen activator: involvement in ovulation.
Endocrinology. 1985 Feb;116(2):516-21. doi: 10.1210/endo-116-2-516.
3
Intrafollicular distribution of plasminogen activators and their hormonal regulation in vitro.卵泡内纤溶酶原激活剂的分布及其体外激素调节
Endocrinology. 1986 Oct;119(4):1588-93. doi: 10.1210/endo-119-4-1588.
4
Changes in and partial identification of the plasminogen activator and plasminogen activator inhibitor systems during ovarian follicular maturation in the pig.猪卵巢卵泡成熟过程中纤溶酶原激活物和纤溶酶原激活物抑制剂系统的变化及部分鉴定
Biol Reprod. 1990 Oct;43(4):636-42. doi: 10.1095/biolreprod43.4.636.
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LH-induced inhibition of follicular androgen formation requires intact steroidogenesis.促黄体生成素诱导的卵泡雄激素生成抑制需要完整的类固醇生成。
Mol Cell Endocrinol. 1982 Jun;27(1):67-75. doi: 10.1016/0303-7207(82)90063-6.
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Effects of luteinizing hormone, progesterone, testosterone, estradiol and corticosterone on ovulation and luteinizing hormone release in hens treated with aminoglutethimide.促黄体生成素、孕酮、睾酮、雌二醇和皮质酮对用氨鲁米特处理的母鸡排卵和促黄体生成素释放的影响。
Biol Reprod. 1984 Mar;30(2):278-88. doi: 10.1095/biolreprod30.2.278.
7
Levels of follicle-stimulating hormone, luteinizing hormone, oestradiol-17 beta and progesterone, and follicular growth in the pseudopregnant rat.假孕大鼠体内促卵泡激素、黄体生成素、雌二醇-17β和孕酮水平以及卵泡生长情况
J Endocrinol. 1975 Jan;64(1):37-47. doi: 10.1677/joe.0.0640037.
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[Correlation between progesterone and plasminogen activator in rat ovaries during the ovulatory process].[大鼠排卵过程中卵巢内孕酮与纤溶酶原激活物的相关性]
Nihon Sanka Fujinka Gakkai Zasshi. 1985 Feb;37(2):247-56.
9
Molecular aspects of mammalian ovulation.哺乳动物排卵的分子机制
Exp Clin Endocrinol Diabetes. 1999;107(1):1-11. doi: 10.1055/s-0029-1212066.
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Disruption of follicular maturation and delay of ovulation after administration of the antiprogesterone RU486.抗孕激素RU486给药后卵泡成熟的破坏和排卵延迟。
J Clin Endocrinol Metab. 1987 Dec;65(6):1135-40. doi: 10.1210/jcem-65-6-1135.

引用本文的文献

1
Midcycle administration of a progesterone synthesis inhibitor prevents ovulation in primates.在灵长类动物中,在月经周期中期给予孕酮合成抑制剂可阻止排卵。
Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):1897-901. doi: 10.1073/pnas.93.5.1897.