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外源性GM1神经节苷脂的唾液酸残基在大鼠肝脏中被循环利用以用于唾液糖缀合物的生物合成。

The sialic acid residue of exogenous GM1 ganglioside is recycled for biosynthesis of sialoglycoconjugates in rat liver.

作者信息

Ghidoni R, Trinchera M, Sonnino S, Chigorno V, Tettamanti G

机构信息

Department of Medical Chemistry and Biochemistry, University of Milan, Italy.

出版信息

Biochem J. 1987 Oct 1;247(1):157-64. doi: 10.1042/bj2470157.

Abstract

In order to assess metabolic recycling of sialic acid, GM1 ganglioside [nomenclature of Svennerholm (1964) J. Lipid. Res. 5, 145-155; IUPAC-IUB Recommendations (1977) Lipids 12, 455-468], 14C-radiolabelled at the acetyl group of sialic acid, was intravenously injected into Wistar rats, and the presence of radioactive sialic acid in liver sialoglycolipids (gangliosides) and sialoglycoproteins was ascertained. A time-course study (20 min-72 h) showed that the radioactivity present in the liver distributed in the following fractions, with reciprocal proportion varying with time: the protein (glycoprotein) fraction, the ganglioside fraction and the diffusible fraction, which contained low-Mr compounds, including sialic acid. Ganglioside-linked radioactivity gradually decreased with time; protein-linked radioactivity appeared soon after injection (20 min), reached a maximum around 20 h, then slowly diminished; diffusible radioactivity provided a sharp peak at 4 h, then rapidly decreased till disappearing after 40 h. The behaviour of bound radioactivity in the individual liver gangliosides was as follows: (a) rapid diminution with time in GM1, although with a lower rate at the longer times after injection; (b) early appearance (20 min) with a peak at 1 h, followed by continuous diminution, in GM2; (c) early appearance (20 min), peak at 1 h, diminution till 4 h, followed by a plateau, in GM3; (d) appearance at 60 min, maximum around 40 h and slow diminution thereafter, in GD1a, GD1b and GT1b. A detailed study, accomplished at 40 h after injection, demonstrated that almost all radioactivity present in the protein fraction was released by mild acid treatment and recovered in purified sialic acid; most of radioactive glycoprotein-bound sialic acid was releasable by sialidase action. In addition, the radioactivity present in the different gangliosides was exclusively carried by sialic acid and present in both sialidase-resistant and sialidase-labile residues. Only in the case of GD1a was the specific radioactivity of sialidase-resistant sialic acid superior to that of sialidase-releasable sialic acid. The results obtained lead to the following conclusions: (a) radioactive GM3 and GM2 were produced by degradation of GM1 taken up; GM3 originated partly by a process of neosynthesis; (b) radioactive GM1 consisted in part of residual exogenous GM1 and in part of a neosynthetized product; (c) radioactive GD1a originated in part by direct sialylation of GM1 taken up and in part by a neosynthetic process; (d) radioactive GD1b and GT1b resulted only from neosynthesis.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

为了评估唾液酸的代谢循环,将在唾液酸乙酰基处用(^{14}C)放射性标记的GM1神经节苷脂[斯文纳霍尔姆(1964年)《脂质研究杂志》5卷,145 - 155页;国际纯粹与应用化学联合会 - 国际生物化学联合会建议(1977年)《脂质》12卷,455 - 468页]静脉注射到Wistar大鼠体内,并确定肝脏唾液糖脂(神经节苷脂)和唾液糖蛋白中放射性唾液酸的存在情况。一项时间进程研究(20分钟 - 72小时)表明,肝脏中存在的放射性物质分布在以下组分中,其相互比例随时间变化:蛋白质(糖蛋白)组分、神经节苷脂组分和可扩散组分,可扩散组分包含低分子量化合物,包括唾液酸。与神经节苷脂相连的放射性随时间逐渐降低;与蛋白质相连的放射性在注射后不久(20分钟)出现,在约20小时达到最大值,然后缓慢减少;可扩散放射性在4小时出现一个尖峰,然后迅速下降,直至40小时后消失。各个肝脏神经节苷脂中结合放射性的行为如下:(a)GM1中随时间迅速减少,尽管在注射后较长时间速率较低;(b)GM2中早期出现(20分钟),在1小时达到峰值,随后持续减少;(c)GM3中早期出现(20分钟),在1小时达到峰值,在4小时减少,随后趋于平稳;(d)GD1a、GD1b和GT1b中在60分钟出现,在约40小时达到最大值,此后缓慢减少。在注射后40小时进行的详细研究表明,蛋白质组分中几乎所有存在的放射性物质经温和酸处理后释放,并在纯化的唾液酸中回收;大多数与糖蛋白结合的放射性唾液酸可通过唾液酸酶作用释放。此外,不同神经节苷脂中存在的放射性仅由唾液酸携带,且存在于抗唾液酸酶和对唾液酸酶敏感的残基中。仅在GD1a的情况下,抗唾液酸酶唾液酸的比放射性高于可被唾液酸酶释放的唾液酸。所得结果得出以下结论:(a)放射性GM3和GM

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b430/1148383/4e0b4674e42e/biochemj00246-0162-a.jpg

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