Wenger D A, Sattler M, Kudoh T, Snyder S P, Kingston R S
Science. 1980 Jun 27;208(4451):1471-3. doi: 10.1126/science.7189903.
Three Siamese cats were found to have a progressive neurological disease that became obvious when they were 4 to 5 months of age. Their brains contained an excess of GM2 and GM3 gangliosides, and their livers a nine- to tenfold excess of sphingomyelin and cholesterol. A total deficiency of lysosomal (pH 5.0) sphingomyelinase was found in the leukocytes, liver, and brain of the cats, although the activity of the microsomal (pH 7.4, magnesium-dependent) sphingomyelinase was normal in brain. These cats appear to have a genetic disease identical to Niemann-Pick disease type A.
三只暹罗猫被发现患有进行性神经疾病,在4至5个月大时症状变得明显。它们的大脑中含有过量的GM2和GM3神经节苷脂,肝脏中的鞘磷脂和胆固醇含量则高出九至十倍。在这些猫的白细胞、肝脏和大脑中发现溶酶体(pH 5.0)鞘磷脂酶完全缺乏,尽管微粒体(pH 7.4,依赖镁)鞘磷脂酶在大脑中的活性正常。这些猫似乎患有与A型尼曼-匹克病相同的遗传疾病。