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辐射的急性和慢性效应揭示了mdx小鼠肌病的隐匿性持续存在。

Covert persistence of mdx mouse myopathy is revealed by acute and chronic effects of irradiation.

作者信息

Pagel C N, Partridge T A

机构信息

MRC Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London, UK.

出版信息

J Neurol Sci. 1999 Apr 1;164(2):103-16. doi: 10.1016/s0022-510x(99)00061-1.

Abstract

To compare muscle fiber loss in young and old mdx mice, we have blocked regeneration in one leg with a high dose (18 Gy) of X-rays administered at two ages; 16 days, just prior to the onset of the myopathy, and 15 weeks, when the myopathy is considered to be quiescent. Mice were examined 4 days after irradiation to look for acute effects, or after 6 weeks to look for cumulative effects. Tibial length, muscle weight, muscle fiber size, fiber number and histological changes were recorded. Signs of acute damage to muscle fibers, leakage of Procion Orange dye into fibers and loss of creatine kinase from the fibers were also examined. Irradiation caused no acute or chronic damage to muscle fibers; on the contrary, in the youngest mdx mice, irradiation delayed the onset of the disease. However, in mdx but not in normal mice, there was a loss of muscle mass and fiber number in irradiated by comparison with the non-irradiated contra-lateral muscles. This loss, attributed to fiber necrosis in the absence of regeneration, was as great in animals irradiated at 15 weeks as in those irradiated at 16 days. Such persistence of muscle fiber necrosis contradicts the standard view of the mdx mouse and establishes it as a closer model of Duchenne muscular dystrophy than is generally appreciated.

摘要

为了比较年轻和年老的mdx小鼠的肌纤维损失情况,我们在两个年龄段用高剂量(18 Gy)的X射线阻断了一条腿的再生;一个是在肌病发作前16天,另一个是在15周时,此时肌病被认为处于静止期。在照射后4天检查小鼠以寻找急性效应,或在6周后检查以寻找累积效应。记录胫骨长度、肌肉重量、肌纤维大小、纤维数量和组织学变化。还检查了肌纤维急性损伤的迹象、普施安橙染料渗入纤维以及肌酸激酶从纤维中流失的情况。照射未对肌纤维造成急性或慢性损伤;相反,在最年幼的mdx小鼠中,照射延迟了疾病的发作。然而,与未照射的对侧肌肉相比,mdx小鼠(而非正常小鼠)照射后出现了肌肉质量和纤维数量的损失。这种损失归因于在没有再生的情况下纤维坏死,在15周时照射的动物中与在16天照射的动物中一样严重。这种肌纤维坏死的持续性与mdx小鼠的标准观点相矛盾,并表明它是比通常所认为的更接近杜兴氏肌营养不良症的模型。

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