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经插管注入大鼠体内的[1-14C]多萜醇的吸收与分布。

Absorption and distribution of [1-14C]dolichol intubated into rats.

作者信息

Crick D C, Carroll K K

出版信息

Biochem Cell Biol. 1987 Apr;65(4):317-20. doi: 10.1139/o87-041.

Abstract

[1-14C]Dolichol was mixed in vitro with sunflower seed oil and intubated into rats. Radioactivity began to appear in the blood at 3 h and peaked after about 6 h. The absorbed radioactivity was rapidly cleared from the blood. At 7.5 h postintubation two thirds of the radioactivity in the serum was associated with chylomicrons and about one quarter with the high density lipoproteins. At 12 h the proportion of the radioactivity in the chylomicrons had fallen to one third and that in the high density lipoproteins had increased to one half of the total. Less than 0.02% of the dose was found in the tissues after 12 h. Liver and blood each contained about one third of the total, with smaller amounts in the lungs and spleen. The heart, testes, brain, and kidneys contained only traces of radioactivity. After 12 h most of the radioactivity in the tissues and feces was present as [1-14C]dolichol. The radioactive compounds in the urine (about 0.05% of the dose) were more polar than [1-14C]dolichol as determined by thin-layer chromatography.

摘要

将[1-14C]多萜醇在体外与向日葵籽油混合后给大鼠插管注入。3小时后血液中开始出现放射性,约6小时后达到峰值。吸收的放射性物质迅速从血液中清除。插管后7.5小时,血清中三分之二的放射性与乳糜微粒相关,约四分之一与高密度脂蛋白相关。12小时时,乳糜微粒中放射性的比例降至三分之一,高密度脂蛋白中的比例增至总量的二分之一。12小时后,组织中发现的剂量不到0.02%。肝脏和血液各占总量的约三分之一,肺和脾脏中的量较少。心脏、睾丸、大脑和肾脏仅含有微量放射性。12小时后,组织和粪便中的大部分放射性以[1-14C]多萜醇形式存在。通过薄层色谱法测定,尿液中的放射性化合物(约占剂量的0.05%)比[1-14C]多萜醇极性更强。

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