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通过接种源自麻风瘤且可培养的分支杆菌HI-75在裸鼠中产生模拟麻风性神经病的实验性神经损伤

[An experimental nerve lesion simulating leprous neuropathy produced in the nude mice by the inoculation of a leproma-derived and cultivable mycobacterium HI-75].

作者信息

Sidik H

机构信息

1st Department of Pathology, Kyorin University School of Medicine, Tokyo, Japan.

出版信息

Nihon Hansenbyo Gakkai Zasshi. 1996 Nov;65(3):174-9. doi: 10.5025/hansen.65.174.

Abstract

Among the lesions caused by mycobacteriosis, peripheral neuropathy has been regarded as the pathognomonic one peculiar to leprosy which is caused only by M. leprae (ML) which can not be cultivated. If that whole sentence is correct, no past report should be in existence concerning the peripheral neuropathy caused by the experimental inoculation of certain cultivated mycobacterium and not of ML. There was, however an exception challenging to that theory which was done by Sasaki et al. in 1985. The author, therefore, tried to reproduce this type of lesion in the nude mice modifying their method to know whether a leproma derived and cultivable mycobaceterium HI 75 (III 75) still have the ability to cause neuropathy as they observed. The mycobacterium utilized in the study was originally separated from a leproma by Skinsnes et al. as M. leprae (ML) III 75 in 1975 and was identified as M scrofulaceum (MS) by Stanford et al. in 1977. The strain was kept on cultivating in his laboratory till 1984 and in our thereafter. The groups of mice served for the present experiments consisted of two. The mice in the first group were infected intravenously and those in the latter group were by subcutaneous injections in the cheeks mixed with hyaluronic acid. The first one was unsuccessful to make remarkable neuropathy, however, the second one showed the marked invasions of the bacilli in peripheral nerves encompassed by numerous macrophages which were heavily loaded with the mycobacteria. The author believes that the present result is helpful to solve the question about the differences of the characteristics of HI-75 before and after causing neuropathy in vivo, the mutual relationship between ML, MS and III 75 and the causative organism beside ML if present.

摘要

在分枝杆菌病引起的病变中,周围神经病变一直被视为仅由不能培养的麻风分枝杆菌(ML)引起的麻风病所特有的特征性病变。如果整个句子是正确的,那么就不应该有关于通过实验接种某些可培养分枝杆菌而非ML引起周围神经病变的既往报告。然而,1985年Sasaki等人的研究是对该理论的一个挑战例外。因此,作者尝试通过修改他们的方法在裸鼠中重现这种类型的病变,以了解源自麻风瘤且可培养的分枝杆菌HI 75(III 75)在体内是否仍具有如他们所观察到的引起神经病变的能力。本研究中使用的分枝杆菌最初由Skinsnes等人于1975年从麻风瘤中分离出来,鉴定为麻风分枝杆菌(ML)III 75,1977年被Stanford等人鉴定为瘰疬分枝杆菌(MS)。该菌株在他的实验室一直培养到1984年,之后在我们实验室培养。用于本实验的小鼠分为两组。第一组小鼠通过静脉注射感染,后一组通过皮下注射到脸颊并与透明质酸混合感染。然而,第一种方法未能引起明显的神经病变,而第二种方法显示杆菌明显侵入周围神经,周围有大量巨噬细胞包围,这些巨噬细胞大量负载着分枝杆菌。作者认为,目前的结果有助于解决关于HI - 75在体内引起神经病变前后特征差异、ML、MS和III 75之间的相互关系以及除ML外是否存在致病生物体的问题。

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