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儿茶酚雌激素诱导延迟着床大鼠开始着床。

Catechol oestrogen induced initiation of implantation in the delayed implanting rat.

作者信息

Kantor B S, Dey S K, Johnson D C

出版信息

Acta Endocrinol (Copenh). 1985 Jul;109(3):418-22. doi: 10.1530/acta.0.1090418.

DOI:10.1530/acta.0.1090418
PMID:4024853
Abstract

In the rat oestrogen is essential for induction of implantation in a progesterone primed uterus. The ability of the catechol oestrogens, 4-hydroxy-oestradiol (4-OH-E2) and 2-hydroxy-oestradiol (2-OH-E2) to initiate the implantation process (blue reaction, indicative of increased endometrial capillary permeability at the location of the blastocyst) in hypophysectomized delayed implanting rats was compared to that of oestradiol-17 beta (E2). Delayed implantation was maintained by daily administration of 2 mg of progesterone. A single sc injection of 100 ng of E2 or 400 ng of 4-OH-E2 consistently initiated implantation in all animals. When delivered sc via osmotic minipumps at a constant release rate of 10 ng/microliters/h, implantation of a full complement of embryos was obtained with E2 given for 6 or 24 h. This dose 4-OH-E2 was ineffective when administered for 24 h. However, 25 ng/microliters/h for 24 h was effective. When the dose was increased to 50 ng/microliters/h implantation was evident in the majority of animals exposed to the hormone for 6 or 8 h; all animals implanted when this dose was given for 24 h. In contrast, 2-OH-E2 given at 50 ng/microliters/h for 24 h was totally ineffective. When the dose of the latter steroid was raised to 200 ng/microliters/h implantation was achieved in half of the animals when exposure was 24 h. The results suggest that when administered systemically, 4-OH-E2 is less potent than E2, but more potent than 2-OH-E2, for initiating implantation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠中,雌激素对于在已用孕酮预处理的子宫中诱导着床至关重要。将儿茶酚雌激素4-羟基雌二醇(4-OH-E2)和2-羟基雌二醇(2-OH-E2)启动着床过程(蓝色反应,表明胚泡着床部位子宫内膜毛细血管通透性增加)的能力,与17β-雌二醇(E2)在垂体切除的延迟着床大鼠中的能力进行了比较。通过每日给予2mg孕酮维持延迟着床状态。单次皮下注射100ng E2或400ng 4-OH-E2可使所有动物均持续启动着床。当通过渗透微型泵以10ng/微升/小时的恒定释放速率皮下给药时,给予E2 6或24小时可使全部胚胎着床。该剂量的4-OH-E2给药24小时无效。然而,25ng/微升/小时给药24小时有效。当剂量增加到50ng/微升/小时时,大多数暴露于该激素6或8小时的动物出现着床;给予该剂量24小时时所有动物均着床。相比之下,以50ng/微升/小时给药24小时的2-OH-E2完全无效。当后一种类固醇的剂量提高到200ng/微升/小时时,暴露24小时的动物中有一半实现了着床。结果表明,全身给药时,4-OH-E2启动着床的效力低于E2,但高于2-OH-E2。(摘要截短至250字)

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1
Catechol oestrogen induced initiation of implantation in the delayed implanting rat.儿茶酚雌激素诱导延迟着床大鼠开始着床。
Acta Endocrinol (Copenh). 1985 Jul;109(3):418-22. doi: 10.1530/acta.0.1090418.
2
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Catechol estradiol induced implantation in the mouse.儿茶酚雌二醇诱导小鼠着床。
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Studies on the temporal pattern of prostaglandin synthesis in the uterus of the delayed implanting rat with or without implantation inducing stimuli.对有或没有植入诱导刺激的延迟着床大鼠子宫中前列腺素合成的时间模式的研究。
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