Effect of prostaglandin E2 or prostaglandin synthesis inhibitors on human gonadotrophins and prolactin.

Eicosanoids Pub Date : 1992-01-01
M Toppozada, F Gerges, H Khalil, S Marzouk, A Kholeif
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Abstract

A role for prostaglandins (PGs) in the release of pituitary hormones in humans is controversial. The effect of PGE2 or PG synthesis inhibitors on gonadotrophin and prolactin (PRL) levels was evaluated in 50 volunteers (25 males and 25 females). Forty cases in four equal groups (Group I & II were males and group III & IV were females) received iv infusion of PGE2 in one cycle and non-steroidal anti-inflammatory drugs (NSAID) [Indomethacin or Naproxen] in the subsequent cycle. Control groups A & B (5 males and 5 females) received saline infusions in one cycle and placebo capsules in the next cycle. Neither PGE2 nor any of the two NSAID altered the basal levels of FSH or LH significantly. PGE2 infusions in males depressed PRL levels significantly two hours after the onset of infusions. Indomethacin raised PRL levels while Naproxen did not. In women, a similar response was also observed but prolactin levels decreased earlier (30 min from the PGE2 infusion). These data indicate a probable role for PGE2 or other prostanoids as well in the regulation of human PRL release but not in gonadotrophin secretion.

前列腺素E2或前列腺素合成抑制剂对人促性腺激素和催乳素的影响。
前列腺素(pg)在人类垂体激素释放中的作用是有争议的。在50名志愿者(25名男性和25名女性)中评估了PGE2或PG合成抑制剂对促性腺激素和催乳素(PRL)水平的影响。四组40例患者(男性为I、II组,女性为III、IV组)在一个周期内静脉滴注PGE2,在后续周期内静脉滴注非甾体抗炎药(NSAID)[吲哚美辛或萘普生]。对照组A组和B组(男5名,女5名)在一个周期内注射生理盐水,在下一个周期内服用安慰剂胶囊。PGE2和两种非甾体抗炎药均未显著改变FSH或LH的基础水平。注射PGE2后2小时,雄性小鼠PRL水平明显降低。吲哚美辛提高了PRL水平,而萘普生没有。在女性中,也观察到类似的反应,但催乳素水平较早下降(输注PGE2后30分钟)。这些数据表明,PGE2或其他前列腺素也可能在调节人类PRL释放中发挥作用,但在促性腺激素分泌中不起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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