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氯米帕明引起的睡眠障碍并不损害其催乳素释放作用。

Clomipramine-induced sleep disturbance does not impair its prolactin-releasing action.

作者信息

Follenius M, Spiegel K, Gronfier C, Saini J, Brandenberger G

机构信息

Laboratoire de Physiologie et de Psychologie Environnementales CNRS, Strasbourg, France.

出版信息

J Endocrinol Invest. 1994 Jun;17(6):417-23. doi: 10.1007/BF03347728.

Abstract

The present study was undertaken to examine the role of sleep disturbance, induced by clomipramine administration, on the secretory rate of prolactin (PRL) in addition to the direct drug effect. Two groups of supine subjects were studied under placebo-controlled conditions, one during the night, when sleeping (n = 7) and the other at daytime, when awake (n = 6). Each subject received a single 50 mg dose of clomipramine given orally 2 hours before blood collection. Plasma PRL concentrations were analysed at 10 min intervals and underlying secretory rates calculated by a deconvolution procedure. For both experiments the drug intake led to significant increases in PRL secretion, acting preferentially on tonic secretion as pulse amplitude and frequency did not differ significantly from corresponding control values. During the night clomipramine ingestion altered the complete sleep architecture in that it suppressed REM sleep and the sleep cycles and induced increased wakefulness. As the relative increase in PRL secretion expressed as a percentage of the mean did not significantly differ between the night and day time studies (46 +/- 19% vs 34 +/- 10%), it can be concluded that the observed sleep disturbance did not interfere with the drug action per se. The presence of REM sleep was shown not to be a determining factor either for secretory pulse amplitude and frequency, as, for both, mean nocturnal values were similar with and without prior clomipramine ingestion.

摘要

本研究旨在探讨由氯米帕明给药引起的睡眠障碍对催乳素(PRL)分泌率的作用,以及药物的直接效应。在安慰剂对照条件下对两组仰卧受试者进行了研究,一组在夜间睡眠时(n = 7),另一组在白天清醒时(n = 6)。在采血前2小时,每位受试者口服50 mg单剂量氯米帕明。每隔10分钟分析血浆PRL浓度,并通过反卷积程序计算潜在分泌率。在两个实验中,药物摄入均导致PRL分泌显著增加,主要作用于紧张性分泌,因为脉冲幅度和频率与相应的对照值无显著差异。夜间服用氯米帕明改变了整个睡眠结构,抑制了快速眼动睡眠和睡眠周期,并导致清醒增加。由于以平均值的百分比表示的PRL分泌相对增加在夜间和白天研究之间无显著差异(46±19%对34±10%),可以得出结论,观察到的睡眠障碍本身并未干扰药物作用。快速眼动睡眠的存在也不是分泌脉冲幅度和频率的决定因素,因为对于这两者,夜间平均值在服用氯米帕明前后相似。

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