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采用红细胞啮齿动物微核试验对吡非尼酮进行遗传毒性评价。

Genotoxic evaluation of pirfenidone using erythrocyte rodent micronucleus assay.

机构信息

Instituto de Biología Molecular en Medicina y Terapia Génica, Centro Universitario de Ciencias de Salud, Universidad de Guadalajara, Mexico.

出版信息

Food Chem Toxicol. 2012 Aug;50(8):2760-5. doi: 10.1016/j.fct.2012.05.049. Epub 2012 Jun 7.

Abstract

Pirfenidone is a non-steroidal antifibrotic compound that has been proposed in clinical protocols and experimental studies as a pharmacological treatment for fibroproliferative diseases. The objective of this study was to determine the genotoxicity or cytotoxicity of three doses of pirfenidone using the micronuclei test in peripheral blood erythrocytes of rodent models. Pirfenidone was administered orally to Balb-C mice for 3 days, and also was administered topically to hairless Sprague Dawley rats during the final stage of gestation. Mice were sampled every 24 h over the course of 6 days; pregnant rats were sampled every 24 h during the last 6 days of gestation, and pups were sampled at birth. Blood smears were analyzed and the frequencies of micronucleated erythrocytes (MNEs), micronucleated polychromatic erythrocytes (MNPCEs), and the proportion of polychromatic erythrocytes (PCEs), were recorded in samples from mice, pregnant rats and rat neonates. Increases in MN frequencies (p<0.03) were noted only in the positive control groups. No genotoxic effects or decreased PCE values were observed neither in newborn rats transplacentally exposed to pirfenidone, or in two adult rodent models when pirfenidone was administered orally or topically.

摘要

吡非尼酮是一种非甾体抗纤维化化合物,已在临床方案和实验研究中被提议作为纤维增生性疾病的药理学治疗方法。本研究的目的是使用外周血红细胞微核试验来确定三种剂量的吡非尼酮的遗传毒性或细胞毒性。将吡非尼酮口服给予 Balb-C 小鼠 3 天,并在无毛 Sprague Dawley 大鼠妊娠末期进行局部给药。在 6 天的过程中,每隔 24 小时对小鼠进行采样;在妊娠的最后 6 天,每隔 24 小时对怀孕的大鼠进行采样,并在出生时对幼鼠进行采样。分析血涂片,并记录来自小鼠、怀孕大鼠和大鼠幼仔的微核红细胞(MNEs)、微核多染红细胞(MNPCEs)和多染红细胞(PCEs)的频率。仅在阳性对照组中观察到 MN 频率增加(p<0.03)。无论是在新生大鼠经胎盘暴露于吡非尼酮,还是在口服或局部给予吡非尼酮的两种成年啮齿动物模型中,均未观察到遗传毒性作用或 PCE 值降低。

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