新生大鼠口服n -乙酰-(14C)神经氨酰基乳糖和n -乙酰-(14C)神经氨酸在各器官的吸收和分布。

W Witt, H von Nicolai, F Zilliken
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引用次数: 36

摘要

将CMP-NeuNAc酶促制的n -乙酰-(14C)神经氨酰基-(α,2, 3)乳糖和泌乳大鼠乳腺颗粒酶组分的乳糖口服给新生大鼠,观察其与游离n -乙酰-(14C)神经氨酸的摄取和分布关系。在孵育前和孵育期间,新生儿被允许与母亲呆在一起,孵育时间长达6小时。在这段时间内,70%的给定剂量被排出,30%留在体内。(14C) neunac -乳糖活性在应用1.5 h后出现在血液、尿液和组织中,分别在3 h和6 h后达到最大值。肝、脾和脑的摄取量最高。与游离的(14C)NeuNAc相比,三糖的吸收延迟了30分钟。曲线的时间过程显示(14C)NeuNAc在组织中的积累速度较慢但较高,这表明(14C)NeuNAc从(14C)NeuNAc-乳糖中得到了更好的利用,或者器官对三糖的吸收存在特殊性。
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Uptake and distribution of orally applied N-acetyl-(14C)neuraminosyl-lactose and N-acetyl-(14C)neuraminic acid in the organs of newborn rats.

N-acetyl-(14C)neuraminosyl-(alpha,2 leads to 3)lactose enzymatically prepared of CMP-NeuNAc and lactose by a particulate enzyme fraction from lactating rat mammary gland was applied orally to newborn rats and examined for uptake and distribution in relation to those of free N-acetyl-(14C)neuraminic acid. The neonates were allowed to stay with their mother before and during the incubation time up to 6 h. Within this time 70% of the given dose was excreted while 30% was retained in the body. (14C)NeuNAc-lactose activity appeared 1.5 h after application in blood, urine, and tissues and attained maximum values after 3 and 6 h, respectively. The highest uptake occurred in liver, spleen, and brain. The absorption of the trisaccharide was delayed by 30 min compared with free (14C)NeuNAc. The time courses of the curves show a slower but higher accumulation in the tissues suggesting a better utilization of the (14C)NeuNAc from (14C)NeuNAc-lactose or pecularities in the absorption of the trisaccharide by the organs.

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