Suppr超能文献

雄性大鼠十氢化萘吸入性肾毒性短期模型的建立。

Development of a short-term model of decalin inhalation nephrotoxicity in the male rat.

作者信息

Stone L C, McCracken M S, Kanerva R L, Alden C L

出版信息

Food Chem Toxicol. 1987 Jan;25(1):35-41. doi: 10.1016/0278-6915(87)90305-x.

Abstract

Fischer 344 male rats and C57BL/6 male mice were exposed 'continuously' (22 hr/day, 7 days/wk) for 20, 28 or 35 days to a model compound, decalin, at 0, 25, 62.5 or 125 ppm. Fischer 344 female rats were exposed 'continuously' to decalin at 0 or 125 ppm for 28 days. No histopathological changes were observed in selected organs of female rats or male mice exposed to up to 125 ppm decalin for 28 or 35 days, respectively. However, kidney lesions were observed in all three test groups of male rats after 20, 28 and 35 days' exposure. The nephrotoxicity was characterized by the formation of hyaline droplets in the cytoplasm of proximal convoluted tubule epithelial cells, by the presence of granular casts at the outer zone of the medulla, and by chronic nephrosis. These changes were time and dose dependent and were identical to the renal toxicity that has been reported to occur in male rats following 90 days of continuous exposure to decalin by inhalation. No histopathological effects were observed in the heart, liver, lung or nasal turbinates of male rats. Our results indicate a sex and species specificity for the kidney toxicity. This leads to questions with regard to the appropriateness of using the male rat to assess the potential inhalation toxicity of volatile hydrocarbons. By producing nephrotoxicity in less than 90 days, decalin may now be used to examine, in a well-defined manner, the effect on nephrotoxicity of variables such as dose, exposure regimen, sex, species, and route of exposure. Data from these studies can be used to ascertain whether or not the male rat is an appropriate test animal for predicting potential human nephrotoxic responses to volatile chemicals such as perfumes and perfume raw materials.

摘要

将Fischer 344雄性大鼠和C57BL/6雄性小鼠“持续”(每天22小时,每周7天)暴露于浓度为0、25、62.5或125 ppm的模型化合物萘满中20、28或35天。将Fischer 344雌性大鼠“持续”暴露于浓度为0或125 ppm的萘满中28天。分别暴露于浓度高达125 ppm萘满28天或35天的雌性大鼠或雄性小鼠的选定器官中未观察到组织病理学变化。然而,在暴露20、28和35天后,所有三个雄性大鼠试验组均观察到肾脏病变。肾毒性的特征是近端曲管上皮细胞胞质中形成透明滴、髓质外区出现颗粒管型以及慢性肾病。这些变化具有时间和剂量依赖性,并且与据报道雄性大鼠连续吸入萘满90天后发生的肾毒性相同。在雄性大鼠的心脏、肝脏、肺或鼻甲中未观察到组织病理学影响。我们的结果表明肾脏毒性存在性别和物种特异性。这引发了关于使用雄性大鼠评估挥发性烃潜在吸入毒性的适用性的问题。通过在不到90天的时间内产生肾毒性,萘满现在可用于以明确的方式研究剂量、暴露方案、性别、物种和暴露途径等变量对肾毒性的影响。这些研究的数据可用于确定雄性大鼠是否是预测人类对香水和香料原料等挥发性化学品潜在肾毒性反应的合适试验动物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验