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盐酸替马沙星对食蟹猴(猕猴)的发育毒性。

Developmental toxicity of temafloxacin hydrochloride in the long-tailed macaque (Macaca fascicularis).

作者信息

Tarantal A F, Lehrer S B, Lasley B L, Hendrickx A G

机构信息

California Primate Research Center, University of California, Davis 95617-8542.

出版信息

Teratology. 1990 Sep;42(3):233-42. doi: 10.1002/tera.1420420307.

DOI:10.1002/tera.1420420307
PMID:2274889
Abstract

The potential developmental toxicity of temafloxacin hydrochloride was studied in the long-tailed macaque (Macaca fascicularis). Ten animals in each of the three drug-treated groups (25, 50, and 100 mg/kg) were administered temafloxacin via nasogastric intubation during gestational days (GD) 20-50. A control group of ten animals received vehicle only. The dams were monitored daily for adverse physical signs and maternal blood samples were collected for analyses of serum progesterone (P), 17 beta-estradiol (E2), and chorionic gonadotropin (CG). In addition, the conceptus was monitored periodically by ultrasound during gestation to confirm growth and viability. Increased maternal toxicity (weight loss, anorexia, emesis) and embryolethality were observed at 100 mg/kg, and a no-observable-adverse-effect-level (NOAEL) of 50 mg/kg was established. The incidence of prenatal mortality was as follows: Control = 1/10 (10%); 25 mg/kg = 1/10 (10%); 50 mg/kg = 2/10 (20%); and 100 mg/kg = 5/10 (50%). Analysis of P, E2, and CG indicated no significant effect of treatment. In addition, no significant differences were observed in embryonic/fetal growth and development when compared to historical controls. No gross structural changes were observed in fetuses exposed to 50 or 100 mg/kg, although one fetus exposed to 25 mg/kg exhibited microphthalmia. This anomaly was considered spontaneous and, therefore, unrelated to treatment.

摘要

在食蟹猴(猕猴属)中研究了盐酸替马沙星的潜在发育毒性。三个药物治疗组(25、50和100 mg/kg)每组10只动物,在妊娠第20至50天通过鼻胃管给予替马沙星。一个由10只动物组成的对照组仅接受赋形剂。每天监测母猴的不良身体体征,并采集母猴血液样本分析血清孕酮(P)、17β-雌二醇(E2)和绒毛膜促性腺激素(CG)。此外,在妊娠期通过超声定期监测胚胎,以确认其生长和活力。在100 mg/kg剂量下观察到母猴毒性增加(体重减轻、厌食、呕吐)和胚胎致死率,并确定无观察到不良反应水平(NOAEL)为50 mg/kg。产前死亡率如下:对照组=1/10(10%);25 mg/kg组=1/10(10%);50 mg/kg组=2/10(20%);100 mg/kg组=5/10(50%)。对P、E2和CG的分析表明治疗无显著影响。此外,与历史对照相比,在胚胎/胎儿生长发育方面未观察到显著差异。暴露于50或100 mg/kg的胎儿未观察到明显的结构变化,尽管一只暴露于25 mg/kg的胎儿出现了小眼畸形。这种异常被认为是自发的,因此与治疗无关。

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