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醋酸乌利司他在食蟹猴中的 39 周口服毒性研究。

A 39-week oral toxicity study of ulipristal acetate in cynomolgus monkeys.

机构信息

PregLem S.A., Chemin du Pré-Fleuri 3, CH-1228 Plan-les-Ouates, Geneva, Switzerland.

出版信息

Regul Toxicol Pharmacol. 2013 Jun;66(1):6-12. doi: 10.1016/j.yrtph.2013.02.013. Epub 2013 Mar 7.

Abstract

Ulipristal acetate (UPA) is a novel Progesterone Receptor Modulator (PRM) and registered for the pre-operative treatment of symptomatic uterine fibroids during 3months. In a study which assessed the potential toxicity of UPA in female cynomolgus monkeys following daily oral administration of 1, 5, or 25mg/kg for 39weeks, UPA was well tolerated with dose-dependent macroscopic and microscopic observations limited to the uterus and oviducts. These findings were considered to be related to the pharmacological action of UPA and showed evidence of partial reversibility. Findings in the endometrium were similar to PRM-associated-endometrial-changes (PAEC) described in PRM-treated women. No adverse effects were found that would raise concerns about potential pre-malignancy. Although the translation of these findings to human is limited by the small study size and species differences, these results from animals chronically exposed to up to 150times the clinical UPA exposure are considered significant and supportive to the chronic administration of UPA for more than 3months in women of reproductive age.

摘要

屈螺酮醋酸酯(UPA)是一种新型孕激素受体调节剂(PRM),已注册用于治疗 3 个月内有症状的子宫肌瘤的术前治疗。在一项评估每日口服 1、5 或 25mg/kg 屈螺酮醋酸酯长达 39 周后对雌性食蟹猴潜在毒性的研究中,屈螺酮醋酸酯具有良好的耐受性,剂量依赖性的宏观和微观观察仅限于子宫和输卵管。这些发现被认为与屈螺酮醋酸酯的药理作用有关,并显示出部分可逆性的证据。子宫内膜的发现与 PRM 治疗女性的 PRM 相关子宫内膜变化(PAEC)相似。未发现任何可能引起对潜在恶性肿瘤的担忧的不良影响。尽管这些发现与人类的相关性受到研究规模小和物种差异的限制,但这些来自长期暴露于临床屈螺酮醋酸酯暴露量 150 倍的动物的结果被认为是重要的,并支持在育龄妇女中持续使用屈螺酮醋酸酯超过 3 个月。

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