Tanaka Masaharu, Homma Kengo, Soejima Aki
Research Unit/Neuroscience, Sohyaku. Innovation Research Division, Mitsubishi Tanabe Pharma Corporation, 1000 Kamoshida-cho, Aoba-ku, Yokohama-shi 227-0033, Japan.
J Toxicol Pathol. 2022 Jan;35(1):129-133. doi: 10.1293/tox.2021-0056. Epub 2021 Oct 1.
We analyzed the histopathological changes and the number of motor neurons (MNs) in the lumbar spinal cord of Cu/Zn superoxide dismutase transgenic (SOD1Tg) mice, which are frequently used as a disease model of amyotrophic lateral sclerosis (ALS). In SOD1Tg mice, hyaline inclusions and foamy vacuoles in the neuronal cell body were observed at 7 weeks of age before neurologic symptoms, and large vacuoles, spheroid formation, and nerve cell aggregation became prominent after 13 weeks of age. The number of healthy MNs was 28.7 to 37.1 cells/animal in wild-type mice and 9.3 to 13.6 cells/animal in transgenic (Tg) mice. Furthermore, the number of MNs, including degenerative neurons, in Tg mice was 27.3-36.1 cells/animal at 18 weeks of age and 17.8-19.6 cells/animal at 21 weeks of age. The present results provide useful information for the development of drugs in ALS treatment.
我们分析了经常用作肌萎缩侧索硬化症(ALS)疾病模型的铜/锌超氧化物歧化酶转基因(SOD1Tg)小鼠腰脊髓中的组织病理学变化和运动神经元(MN)数量。在SOD1Tg小鼠中,在出现神经症状前的7周龄时,在神经元细胞体中观察到透明包涵体和泡沫状空泡,而在13周龄后,大空泡、球状体形成和神经细胞聚集变得明显。野生型小鼠中健康MN的数量为28.7至37.1个细胞/动物,转基因(Tg)小鼠中为9.3至13.6个细胞/动物。此外,Tg小鼠中包括退化神经元在内的MN数量在18周龄时为27.3 - 36.1个细胞/动物,在21周龄时为17.8 - 19.6个细胞/动物。本研究结果为ALS治疗药物的开发提供了有用信息。