Taketomi T, Hara A, Kasama T
Adv Exp Med Biol. 1984;174:419-29. doi: 10.1007/978-1-4684-1200-0_35.
Biochemical analyses of the samples of GM1-gangliosidosis Type 1, Type 2, and Chronic type at autopsy showed that GM1 and asialo-GM1 are markedly increased in the whole cerebral tissues of patients with Type 1 and Type 2, but mainly in the basal ganglia including caudate nucleus and putamen in the Chronic Type as already reported by Kobayashi and Suzuki in 1981. On the other hand, the finding that the Type 1 visceral organs contained unusual glycolipids rather than gangliosides was contrasted to those of Type 2 which seemed less abnormal. The unusual glycolipids included particularly fucolipid I and II consisting of glucose:galactose:N-acetylglucosamine:fucose (1:2:1:1) and (1:3:2:2), respectively. The chemical structure of oligosaccharide moiety of fucolipid I may be identical with Lacto-N-fucopentaose II or Lacto-N-fucopentaose III. The fucolipid II may be proposed to be Lacto-N-difucooctanose.
对1型、2型和慢性型GM1神经节苷脂沉积症尸检样本的生化分析表明,1型和2型患者全脑组织中GM1和脱唾液酸GM1明显增加,但如1981年小林和铃木所报道,慢性型主要在包括尾状核和壳核的基底神经节中增加。另一方面,1型内脏器官含有异常糖脂而非神经节苷脂这一发现,与似乎异常程度较轻的2型形成对比。异常糖脂尤其包括岩藻糖脂I和II,分别由葡萄糖:半乳糖:N-乙酰葡糖胺:岩藻糖(1:2:1:1)和(1:3:2:2)组成。岩藻糖脂I寡糖部分的化学结构可能与乳糖-N-岩藻五糖II或乳糖-N-岩藻五糖III相同。岩藻糖脂II可能被认为是乳糖-N-二岩藻辛糖。