小鼠和大鼠外源性唾液乳糖和粘蛋白中唾液酸的代谢。

U Nöhle, R Schauer
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引用次数: 37

摘要

将n -乙酰基-[4,5,6,7,8,9-14C]神经氨酰基- α(2-3(6)-半乳糖- α(1-4-葡萄糖[(14C]唾液酰基乳糖)和n -乙酰基神经氨酰基- α(2-3(6)-半乳糖- β(1-4)-葡萄糖-1-[3H]醇(唾液酰基-[3H]乳酸)的混合物以及用n -乙酰基和n -甘油三酯-[9-(3)H]神经氨酸标记的猪颌下腺粘蛋白口服给鼠。研究了不同同位素在动物血液、组织和排泄产物中的分布。口服[14C]唾液-乳糖/唾液-[3H]乳醇混合物的一半不变地随尿液排出。另一半被唾液酸酶水解,在一定程度上进一步代谢,其次是30%的14的排泄c-radioactivity免费n -乙酰-(4、5、6、7、8日9-14C]神经氨酸和60%的放射性non-anionic化合物的形式包括过期14 co2在24 h。14 c-radioactivity来源于[14 c] sialyl-lactose / sialyl - [3 h]乳糖醇混合物的尸体仍在小鼠禁食24小时后还不到1%。在喂养良好的小鼠中,唾液酸残留物的代谢量更高。粘蛋白的大部分放射性在24小时内被吸收,约40%的放射性在48小时内通过尿液排出;其中30%为唾液酸,70%为其他阴离子和非阴离子代谢产物。60%的放射性物质留在体内,结合的3h标记唾液酸从肝脏中分离出来。大鼠静脉注射唾液醛- α (2-3)-[3H]乳醇;这种物质在尿液中迅速排出而不分解。这些研究表明,部分与低聚糖和糖蛋白结合的唾液酸可在肠内被唾液苷酶水解并被吸收。随后是游离唾液酸排泄或不同程度的代谢,这显然取决于复合饲料和在消化道中的滞留时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolism of sialic acids from exogenously administered sialyllactose and mucin in mouse and rat.

A mixture of N-acetyl-[4,5,6,7,8,9-14C]neuraminosyl-alpha (2-3(6]-galactosyl-beta (1-4-glucose[( 14C]sialyl-lactose) and N-acetylneuraminosyl-alpha (2-3(6]-galactosyl-beta(1-4)-glucit-1-[3H]ol(sialyl-[3H]lactitol) as well as porcine submandibular gland mucin labeled with N-acetyl- and N-glycoloyl-[9-(3)H]neuraminic acid were administered orally to mice. The distribution of the different isotopes was followed in blood, tissues and excretion products of the animals. One half of the [14C]sialyl-lactose/sialyl-[3H]lactitol mixture given orally was excreted unchanged in the urine. The other half was hydrolysed by sialidase and partly metabolized further, followed by the excretion of 30% of the 14C-radioactivity as free N-acetyl-[4,5,6,7,8,9-14C]neuraminic acid and 60% of this radioactivity in the form of non-anionic compounds including expired 14CO2 within 24 h. The 14C-radioactivity derived from the [14C]sialyl-lactose/sialyl-[3H]lactitol mixture which remained in the bodies of fasted mice after 24 h was less than 1%. In the case of well-fed mice, a higher amount of the sialic acid residues was metabolized. The bulk of radioactivity of the mucin was resorbed within 24 h. About 40% of the radioactivity administered was excreted by the urine within 48 h; 30% of this radioactivity represented sialic acid and 70% other anionic and non-anionic metabolic products. 60% of the radioactivity administered remained in the body, and bound 3H-labeled sialic acids were isolated from liver. Sialyl-alpha (2-3)-[3H]lactitol was injected intravenously into rats; the substance was rapidly excreted in the urine without decomposition. These studies show that part of the sialic acids bound to oligosaccharides and glycoproteins can be hydrolysed in intestine by sialidase and be resorbed. This is followed either by excretion as free sialic acid or by metabolization at variable degrees, which apparently depends on the compound fed and on the retention time in the digestive tract.

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