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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.

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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