Igisu H, Suzuki K
Science. 1984 May 18;224(4650):753-5. doi: 10.1126/science.6719111.
Progressive accumulation of a cytotoxic metabolite, galactosylsphingosine (psychosine), was found in the brain of the twitcher mouse, a mutant caused by genetic deficiency of galactosylceramidase. Similar abnormal accumulation was also found in the brain of the genetic galactosylceramidase deficiency disease in the dog and in human patients (globoid cell leukodystrophy or Krabbe disease). Galactosylphingosine was absent in the brains of normal and heterozygous mice. The finding provides support for the psychosine hypothesis as the biochemical pathogenetic mechanism of globoid cell leukodystrophy. Analogous mechanisms may be important in the pathogenesis of other genetic lysosomal diseases.
在震颤小鼠(一种因半乳糖基神经酰胺酶基因缺陷导致的突变小鼠)的大脑中发现了具有细胞毒性的代谢产物半乳糖基鞘氨醇(精神鞘氨醇)的进行性积累。在患有遗传性半乳糖基神经酰胺酶缺乏症的犬类和人类患者(球状细胞脑白质营养不良或克拉伯病)的大脑中也发现了类似的异常积累。正常小鼠和杂合子小鼠的大脑中不存在半乳糖基鞘氨醇。这一发现为精神鞘氨醇假说作为球状细胞脑白质营养不良的生化发病机制提供了支持。类似的机制可能在其他遗传性溶酶体疾病的发病过程中起重要作用。