年轻瑞士小鼠自发性眼部病变。

Laboratory animal science Pub Date : 1999-06-01
M F Hubert, G Gerin, G Durand-Cavagna
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引用次数: 0

摘要

背景与目的:近交系小鼠是毒性评价的常用方法。由于它们的体积小,这些动物的眼科检查在限制和使用为人类医学设计的仪器方面是困难的。自发性眼部病变的临床表现和发生率应该有助于选择小鼠进行毒性研究,并允许区分并发的自发性眼部病变和可归因于药物或化学物质的病变。方法:于1995年和1996年对约3000只4 ~ 5周龄瑞士小鼠进行眼前检查,了解自发性眼部病变及其发生率。瞳孔扩张(滴入0.5%托品酰胺)后,使用间接检眼镜进行视力评估,必要时使用便携式裂隙灯。结果:晶状体混浊和异质性/突出是前段最常见的表现(高达19%)。在高达4%的小鼠中检测到角膜和虹膜异常。12% ~ 17%的小鼠玻璃体可见玻璃体动脉残余,并有游离体或出血。大约2 - 4%的小鼠患有结缔组织性眼底、视网膜褶皱或视网膜萎缩。少数小鼠出现视网膜萎缩、出血或视网膜血管异常。其余表现包括不完全性睑裂、小眼、突出眼、眼出血和巩膜肿块。结论:由于病情严重或干扰眼部检查,应将受影响的小鼠排除在实验研究之外。因此,在安全性评估毒性研究中需要对小鼠进行眼部检查。
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Spontaneous ophthalmic lesions in young Swiss mice.

Background and purpose: Outbred mice are frequently used in toxicity evaluation. Due to their small size, ophthalmologic examination of such animals is difficult with regard to restraint and use of instruments designed for human medicine. The clinical appearance and incidence of spontaneous ophthalmic lesions should be helpful in selecting mice for toxicity studies and allow distinction between intercurrent spontaneous ocular changes and those attributable to drugs or chemicals.

Methods: Pretest ophthalmologic examinations of about 3,000 4- to 5-week-old Swiss mice, Crl:CD1 (ICR)BR, conducted in 1995 and 1996, provided information about spontaneous ocular changes and their incidence. Eye evaluations were performed after pupil dilatation (0.5% tropicamide instillation), using indirect ophthalmoscopy, and when indicated, a portable slit lamp.

Results: Lenticular opacities and heterogeneity/prominence were the most common findings (up to 19%) in the anterior segment. Abnormalities of the cornea and iris were detected in up to 4% of mice. Hyaloid artery remnant, as well as isolated cases of floating bodies or hemorrhage, was observed in the vitreous of 12 to 17% of mice. Approximately 2 to 4% of mice had colobomatous fundus, retinal fold, or retinal atrophy. A few mice had chorioretinal atrophy, hemorrhage, or abnormal pattern of the retinal vasculature. Remaining findings consisted of incomplete palpebral fissure, microphthalmia, exophthalmia, ophthalmic hemorrhage, and scleral mass.

Conclusions: Due to severity of the condition or interference with ocular examination, affected mice should be eliminated from experimental studies. Hence, pretest ocular examinations of mice are indicated in safety-assessment toxicity studies.

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