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大鼠植入前和植入后时期催乳素抑制对子宫葡萄糖胺合酶活性的影响

Prolactin suppression during pre and post-implantation periods on rat uterine glucosamine synthase activity.

作者信息

Vijayan E, Jayashree J

机构信息

School of Life Sciences, Pondicherry University, India.

出版信息

Indian J Exp Biol. 1993 Apr;31(4):386-8.

PMID:8359840
Abstract

Administration of bromocriptine (Bc), an ergot derivative having dopamine receptor agonist activity, to rats on day 1-5 of pregnancy prevented implantation of blastocysts and significantly suppressed uterine glucosamine 6-phosphate synthase activity. There was no effect on implantation or the enzyme activity when Bc was injected on day 7 or later of pregnancy. Injection of prolactin following Bc partially restored the enzyme activity and increased number of implantation sites. These results indicate that suppression of prolactin on day 1 to 5 of pregnancy causes failure of implantation. Bc on day 9 or later had no effect possibly due to the availability of placental LH/hCG to support the luteal cells.

摘要

在妊娠第1至5天给大鼠注射溴隐亭(Bc),一种具有多巴胺受体激动剂活性的麦角衍生物,可阻止胚泡着床,并显著抑制子宫葡萄糖胺6 - 磷酸合酶活性。在妊娠第7天或之后注射Bc对着床或酶活性没有影响。在注射Bc后注射催乳素可部分恢复酶活性并增加着床部位的数量。这些结果表明,妊娠第1至5天催乳素的抑制导致着床失败。第9天或之后的Bc没有影响,可能是由于胎盘促黄体生成素/人绒毛膜促性腺激素可支持黄体细胞。

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