摘要
利用＾３Ｈ标记Ｄ－聚甘酯，观察了小鼠口服Ｄ－聚甘酯后在各组织和器官尤其是脑的分布特点，并对春血脑屏障的机制进行了初步探讨。实验结果显示，Ｄ－了矣甘酯可以迅速透过血脑屏障，并且除肾脏外，其在脑中的显著性地高于其他组织与器官。Ｄ－聚甘酯在中脑的２显著的高于脑的其他部位。给药３ｈ以后，脑内的Ｄ－聚甘酯９５．８％以原形存在。给小鼠等量的＾３Ｈ－Ｄ－聚甘酯和不同量的Ｄ－聚甘酯，随着Ｄ－聚甘酯量的增加。
The amount of Mannuronicate in the brain was significantly higher than that in other organs except in kidneys after mannuronicate was given rats by oral administration after 48h. Mannuronicate could penetrate blood-brain barrier and was more concentrated in midbrain than in other part of brain. After 3h administration, 95. 8% of Mannuronicate remained intact form. We assumed that Mannuronicate could cross blood-brain barrier aided by a saturable transport system on the basis of the observation that radioactivity in the brain was lower with the increase of Mannuronicate and the same amount of ~3H Mannuronicate
出处
《中国海洋药物》
CAS
CSCD
1999年第2期35-38,23,共5页
Chinese Journal of Marine Drugs
基金
教育部博士点基金资助项目!(编号:97042309)
关键词
D-聚甘酯
分布
血脑屏障
转运机制
Mannuronicate
distribution
blood brain barrier
transport system
