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人妊娠早期使用溴隐亭治疗:对催乳素、性类固醇和胎盘催乳素水平的影响。

Bromocriptine treatment during early human pregnancy: effect on the levels of prolactin, sex steroids and placental lactogen.

作者信息

Ylikorkala O, Kivinen S, Rönnberg L

出版信息

Acta Endocrinol (Copenh). 1980 Nov;95(3):412-5. doi: 10.1530/acta.0.0950412.

Abstract

To elucidate the role of prolactin (Prl) in the endocrinology of early human pregnancy, 28 healthy women were given 5.0-7.5 mg of bromocriptine daily for two weeks between weeks 6-9 of normal gestation. Plasma Prl, oestradiol-17 beta (Oe2), progesterone (P), testosterone (T) and human placental lactogen (hPL) were measured before, and one and two weeks after the start of bromocriptine, and they were compared with those in 22 control women who were followed similarly but without bromocriptine treatment. Bromocriptine treatment induced a significant Prl depression at one week (7.3 +/- 4.3 ng/ml vs 23.7 +/- 11.4 ng/ml) and two weeks (5.3 +/- 2.5 ng/ml vs 31.9 +/- 16.4 ng/ml). Oe2, P, T and hPL levels, however, showed no significant differences between the groups. Two women undergoing bromocriptine treatment (7.1%) and one control women (4.5%) experienced spontaneous incomplete abortion during the study period, but these three already had a low Oe2 level and a low/or undetectable hPL level at the beginning of the study. It is obvious that neither maternal 'hypoprolactinaemia' nor bromocriptine during early human pregnancy interfere with the normal progress of pregnancy or with the normal synthesis of sex steroids and hPL at this time.

摘要

为阐明催乳素(Prl)在人类早期妊娠内分泌学中的作用,28名健康女性在正常妊娠第6至9周期间,每天服用5.0 - 7.5毫克溴隐亭,持续两周。在开始服用溴隐亭之前、之后1周和2周时,测定血浆Prl、雌二醇 - 17β(Oe2)、孕酮(P)、睾酮(T)和人胎盘催乳素(hPL),并与22名同样进行随访但未接受溴隐亭治疗的对照女性进行比较。溴隐亭治疗在1周时(7.3±4.3纳克/毫升对23.7±11.4纳克/毫升)和2周时(5.3±2.5纳克/毫升对31.9±16.4纳克/毫升)引起显著的Prl降低。然而,两组之间的Oe2、P、T和hPL水平没有显著差异。在研究期间,两名接受溴隐亭治疗的女性(7.1%)和一名对照女性(4.5%)发生了自然不全流产,但这三名女性在研究开始时Oe2水平就较低且hPL水平较低或无法检测到。显然,在人类妊娠早期,母体“低催乳素血症”或溴隐亭均不会干扰妊娠的正常进程,也不会干扰此时性类固醇和hPL的正常合成。

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