Study of embryotoxic and teratogenic properties of Medicine No. 60 and evaluation of its effect on the reproductive function of rats.

Pletnev Vladimir Vladimirovich
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引用次数: 1

Abstract

Intramuscular administration of medicine No. 60 at a dose of 1.281 mg/kg (30 times the estimated highest daily dose for humans) when diluted with 1:5 saline solution to pregnant rats from Day 1 to Day 19 of pregnancy does not affect the indicators of pre- and postimplantation death of baby rats. The body weight of the rats exposed to the medicine No. 60 during the prenatal period of development did not differ from the indicators in the control group. The development of offspring in the experimental group during the entire observation period took place without deviation from the terms characteristic of the normal physiological development of animals of this species. As a result of the studies conducted, it was found that intramuscular administration of drug No. 60 at a dose of 1.281 mg/kg in a 1:10 dilution with saline solution, which was 30 times the estimated maximum daily therapeutic dose for humans, did not affect the sexual activity of animals, reproductive indicators (number of live fetuses, body weight of embryos, their craniocaudal size, number of yellow bodies, implantation sites, resorption), or the neonatal development of baby rats. Thus, there was no effect of medicine No. 60 in the test dose of 1.281 mg/kg on the reproductive function of healthy mature rats and does not exhibit embryotoxic and teratogenic activity.
药物60号胚胎毒性和致畸性的研究及其对大鼠生殖功能影响的评价。
在妊娠第1天至第19天,用1:5的生理盐水稀释后,以1.281 mg/kg(人估计最高日剂量的30倍)的剂量肌内给药60号药物,对幼鼠植入前后死亡指标无影响。暴露于60号药的大鼠在产前发育期间的体重与对照组的各项指标没有差异。在整个观察期内,实验组子代的发育均未偏离该物种动物正常生理发育的特征。经研究发现,以生理盐水1:10稀释1.281 mg/kg的剂量肌注60号药物,即人体估计最大日治疗剂量的30倍,不影响动物的性活动、生殖指标(活胎数、胚胎体重、颅趾大小、黄体数、着床部位、吸收),也不影响幼鼠的新生发育。由此可见,试验剂量为1.281 mg/kg的60号药对健康成熟大鼠生殖功能无影响,不表现出胚胎毒性和致畸活性。
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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