Igisu H
Department of Environmental Toxicology, University of Occupational and Environmental Health, Kitakyushu, Japan.
J UOEH. 1989 Dec 1;11(4):487-93. doi: 10.7888/juoeh.11.487.
Psychosine (galactosylsphingosine) is enzymatically synthesized from UDP-galactose and sphingosine and degraded by galactosylceramidase. Galactosylceramidase is genetically deficient in Krabbe disease (globoid cell leukodystrophy) and psychosine accumulates in the brain of humans, dogs or mice affected by the disease. Psychosine has a very potent inhibitory effect on cytochrome c oxidase (COX) in mitochondria. When COX is purified, psychosine does not suppress the enzyme activity. However, a clear inhibitory effect is seen when the enzyme is "reconstituted" with sonicated phosphatidylcholine, suggesting that the inhibition of the enzymatic activity is caused by perturbation of the environment of COX in the mitochondrial membrane. Studies using analogues suggest that the free amino group in the sphingosine moiety plays an important role in exerting the effects of psychosine. The effects of psychosine are not only potent but fast and reversible. It is noteworthy that a powerful inhibitor of cellular respiration is synthesized in mammals' brain, an organ vulnerable to hypoxia.
神经鞘氨醇半乳糖苷(psychosine)可由尿苷二磷酸半乳糖(UDP - galactose)和鞘氨醇通过酶促反应合成,并由半乳糖神经酰胺酶降解。在克拉伯病(球形细胞脑白质营养不良症)中,半乳糖神经酰胺酶存在基因缺陷,导致神经鞘氨醇半乳糖苷在患该病的人类、犬类或小鼠的大脑中蓄积。神经鞘氨醇半乳糖苷对线粒体中的细胞色素c氧化酶(COX)具有非常强的抑制作用。当COX被纯化时,神经鞘氨醇半乳糖苷不会抑制其酶活性。然而,当用超声处理的磷脂酰胆碱对该酶进行“重组”时,可观察到明显的抑制作用,这表明酶活性的抑制是由线粒体膜中COX环境的扰动引起的。使用类似物的研究表明,鞘氨醇部分的游离氨基在发挥神经鞘氨醇半乳糖苷的作用中起重要作用。神经鞘氨醇半乳糖苷的作用不仅强大,而且迅速且可逆。值得注意的是,一种强大的细胞呼吸抑制剂在哺乳动物易受缺氧影响的大脑中合成。