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对震颤小鼠(克拉伯病的酶学真实模型)发病机制的研究。

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease.

作者信息

Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H

机构信息

Department of Pediatrics, Osaka University, Japan.

出版信息

J Neurol Sci. 1990 Dec;100(1-2):124-30. doi: 10.1016/0022-510x(90)90022-f.

Abstract

The twitcher mouse was investigated by examining in vivo synthesis of galactosylceramide (Galcer) and galactosylsphingosine (Galsph) in a sciatic nerve culture, and in vitro enzymic activities for synthesis of Galcer and Galsph in the spinal cord from normal and affected mice. For the in vivo study, the sciatic nerve was incubated for 24 h in medium containing [3H]galactose, or [3H]-sphingosine-labeled Galcer or Galsph. With [3H]galactose, reduced synthesis of Galcer was found as early as 1 week of age and synthesis decreased to about 15% of normal value at 4 weeks. Increased Galsph was detected after 7 days of feeding with galactose. In a study of [3H]sphingosine-labeled Galcer and Galsph feeding, Galcer did not induce Galsph synthesis in either normal or affected mice, and synthesis of Galcer from Galsph was found only in normal mice, suggesting that Galcer was synthesized from sphingosine after hydrolysis of Galsph. In vitro, the activities of UDP-galactose: ceramide galactosyltransferase and UDP-galactose: sphingosine galactosyltransferase were reduced to less than 50% of control after 2 weeks of age in affected mice. We conclude that (1) decreased Galcer was due to impaired synthesis of Galcer, (2) Galsph was synthesized from galactose and not from deacylation of Galcer, and (3) Galsph accumulation was due not to increased synthesis but to decreased hydrolysis.

摘要

通过检测坐骨神经培养物中半乳糖基神经酰胺(Galcer)和半乳糖基鞘氨醇(Galsph)的体内合成,以及正常和患病小鼠脊髓中Galcer和Galsph合成的体外酶活性,对震颤小鼠进行了研究。在体内研究中,将坐骨神经在含有[3H]半乳糖、或[3H]鞘氨醇标记的Galcer或Galsph的培养基中孵育24小时。用[3H]半乳糖时,早在1周龄时就发现Galcer合成减少,4周时合成降至正常值的约15%。用半乳糖喂养7天后检测到Galsph增加。在一项[3H]鞘氨醇标记的Galcer和Galsph喂养研究中,Galcer在正常或患病小鼠中均未诱导Galsph合成,并且仅在正常小鼠中发现从Galsph合成Galcer,这表明Galcer是在Galsph水解后由鞘氨醇合成的。在体外,患病小鼠在2周龄后,UDP-半乳糖:神经酰胺半乳糖基转移酶和UDP-半乳糖:鞘氨醇半乳糖基转移酶的活性降至对照的50%以下。我们得出结论:(1)Galcer减少是由于Galcer合成受损;(2)Galsph是由半乳糖合成而非Galcer的去酰化作用合成;(3)Galsph积累不是由于合成增加而是由于水解减少。

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