大鼠体内镤-233的生化结合与分布。

U Schuppler, F Planas-Bohne, D M Taylor
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引用次数: 7

摘要

静脉注射到雄性Sprague-Dawley大鼠体内后,233Pa与其他元素一样,主要沉积在骨骼中(约70- 80%),但与Pu和Am不同的是,233Pa的肝脏沉积较低,在1至7天内约为2- 3%。大约99%的注入的233Pa在3天内从血浆室中丢失,其清除速度与Pu相当,但远慢于Np, Am或Cm。在进入肝细胞细胞质后,233Pa迅速与一个分子量为200 kDa的未知蛋白和一个分子量为80 kDa的蛋白结合,该蛋白可能是转铁蛋白。在几个小时内,金属迁移到一个大于400kda的蛋白质上,这个蛋白质暂时被确定为铁蛋白。一些233Pa仍然与小配体结合,直到几乎所有的细胞内233Pa都沉积在溶酶体中,或在较小程度上沉积在其他一些尚未确定的细胞器中。
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Biochemical binding and distribution of protactinium-233 in the rat.

Following intravenous injection into male Sprague-Dawley rats 233Pa, like other elements, deposits predominantly in the skeleton (ca. 70-80 per cent), but unlike Pu and Am the liver deposition of 233Pa is low, about 2-3 per cent between 1 and 7 days. About 99 per cent of the injected 233Pa is lost from the plasma compartment in 3 days, a clearance comparable to that of Pu but much slower than that of Np, Am or Cm. On entering the liver cell cytosol 233Pa is bound rapidly to an unidentified protein of molecular mass 200 kDa and to a protein of 80 kDa, which is probably transferrin. Within a few hours the metal migrates to bind to a protein of greater than 400 kDa which has been tentatively identified as ferritin. Some 233Pa remains bound to small ligands until virtually all the intracellular 233Pa has been deposited in the lysosomes, or to a lesser extent in some other, as yet, unidentified organelles.

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