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血小板生成素受体激动剂对妊娠小鼠的影响。

Effect of Thrombopoietin Receptor Agonist on Pregnant Mice.

作者信息

Nakai Kensaku, Misugi Takuya, Kitada Kohei, Kurihara Yasushi, Tahara Mie, Hamuro Akihiro, Nakano Akemi, Koyama Masayasu, Kira Yukimi, Tachibana Daisuke

机构信息

Department of Obstetrics and Gynecology, Osaka City University Graduate School of Medicine, 1-4-3 Asahimachi Abeno-ku Osaka, Osaka 545-8585, Japan.

Department of Research Support Platform, Osaka City University Graduate School of Medicine, 1-4-3 Asahimachi Abeno-ku Osaka, Osaka 545-8585, Japan.

出版信息

Pharmaceutics. 2022 Feb 25;14(3):514. doi: 10.3390/pharmaceutics14030514.

Abstract

Thrombopoietin receptor agonists (TPO-RAs) are an effective treatment for refractory immune thrombocytopenia (ITP). However, the use of TPO-RAs is limited for ITP in pregnant women due to concerns about fetal toxicity. In this study, we examined the effects of romiplostim, one of the TPO-RAs, on pregnant mice. The mice were injected subcutaneously with romiplostim (1, 5, 10, 30, and 100 μg/kg) on gestational days (GD) 1, 8, and 15. We evaluated maternal and fetal platelet and megakaryocyte counts (MK), fetal weight at birth, placental morphology, and miscarriage rates. Romiplostim increased platelet and MK counts in pregnant mice at all doses and in fetuses at doses above 10 µg/kg. Fetal weight at birth was slightly reduced at a dose of 100 μg/kg, but there were no significant differences in placental weight, spiral artery wall thickness, placental growth factor signal changes, or the rate of resorption at that dosage. The dose of romiplostim used clinically for ITP patients (1-10 μg/kg) did not show any adverse effects on pregnant mice. Although the results of the present study are encouraging, until there are more conclusive data, the use of romiplostim should be evaluated individually in severe, life-threatening cases, and all relevant ethical aspects should be considered.

摘要

血小板生成素受体激动剂(TPO-RAs)是治疗难治性免疫性血小板减少症(ITP)的有效药物。然而,由于担心胎儿毒性,TPO-RAs在孕妇ITP治疗中的应用受到限制。在本研究中,我们检测了TPO-RAs之一的罗米司亭对妊娠小鼠的影响。在妊娠第1、8和15天,给小鼠皮下注射罗米司亭(1、5、10、30和100μg/kg)。我们评估了母体和胎儿的血小板及巨核细胞计数(MK)、出生时的胎儿体重、胎盘形态以及流产率。罗米司亭在所有剂量下均增加了妊娠小鼠的血小板和MK计数,在剂量高于10μg/kg时增加了胎儿的血小板和MK计数。在100μg/kg剂量下,出生时的胎儿体重略有降低,但该剂量下胎盘重量、螺旋动脉壁厚度、胎盘生长因子信号变化或吸收速率均无显著差异。临床上用于ITP患者的罗米司亭剂量(1-10μg/kg)对妊娠小鼠未显示任何不良反应。尽管本研究结果令人鼓舞,但在获得更多确凿数据之前,对于严重的、危及生命的病例,应单独评估罗米司亭的使用情况,并应考虑所有相关的伦理问题。

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