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肾上腺素能阻滞剂美托洛尔及其代谢产物OH-美托洛尔在母体血浆、羊水和新生儿毛细血管血中的分布情况。

Disposition of the adrenergic blocker metoprolol and its metabolite OH-metoprolol in maternal plasma, amniotic fluid and capillary blood of the neonate.

作者信息

Lindeberg S, Lundborg P, Regårdh C G, Sandström B

机构信息

Department of Obstetrics and Gynecology, Orebro Medical Center Hospital, Sweden.

出版信息

Eur J Clin Pharmacol. 1987;33(4):363-8. doi: 10.1007/BF00637631.

Abstract

Seven women were treated with metoprolol 50-100 mg twice daily for hypertension in pregnancy. The disposition of metoprolol and one of its metabolites alfa-OH-metoprolol was studied in venous plasma and amniotic fluid during labour, in mixed cord plasma and in capillary blood of the newborn. Peak concentrations of metoprolol and alfa-OH-metoprolol were reached 60 to 120 min after dosing in maternal plasma while the amniotic fluid levels of these compounds continued to increase from 60 to 180 min to the end of the study and were substantially higher than in the plasma after 4 to 5 h. It is postulated that a major fraction of metoprolol and alfa-OH-metoprolol reaches the amniotic fluid via the fetal urine and that the elimination from the amniotic fluid mainly proceeds via diffusion across fetal membranes and transfer across the fetal capillary bed. No measurable concentrations of metoprolol were found in two of the newborns 2 h after delivery. In the remaining four neonates the 2-h concentrations exceeded the corresponding cord plasma levels. In all neonates the alfa-OH-metoprolol levels in the capillary blood were higher 2 h after birth than in cord blood. In two newborns the metabolite levels continued to increase for 5 h and in one the highest blood concentrations of this metabolite was found 20 h after birth. Redistribution of metoprolol from tissue stores followed by metabolism might be the cause of these temporary elevations of the blood levels of metoprolol and alfa-OH-metoprolol.

摘要

七名患有妊娠期高血压的女性接受了美托洛尔治疗,剂量为每日两次,每次50 - 100毫克。在分娩期间,对美托洛尔及其一种代谢物α-羟基美托洛尔在静脉血浆和羊水中的处置情况进行了研究,同时也研究了其在混合脐血和新生儿毛细血管血中的情况。在母体血浆中,给药后60至120分钟达到美托洛尔和α-羟基美托洛尔的峰值浓度,而这些化合物在羊水中的水平从60分钟到180分钟持续升高,直至研究结束,并且在4至5小时后显著高于血浆中的水平。据推测,美托洛尔和α-羟基美托洛尔的大部分是通过胎儿尿液进入羊水的,并且羊水的消除主要是通过跨胎儿膜的扩散和跨胎儿毛细血管床的转运进行的。在两名新生儿出生后2小时未检测到美托洛尔的可测量浓度。在其余四名新生儿中,2小时时的浓度超过了相应的脐血血浆水平。在所有新生儿中,出生后2小时毛细血管血中的α-羟基美托洛尔水平高于脐血中的水平。在两名新生儿中,代谢物水平持续升高5小时,在一名新生儿中,该代谢物的最高血药浓度在出生后20小时被发现。美托洛尔从组织储存中重新分布,随后进行代谢,可能是美托洛尔和α-羟基美托洛尔血药水平暂时升高的原因。

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