Effect of Aflatoxin B1 and Corticosterone on Ribosome-distributions between Free and Membrane-bound States and between Monosomes and Polysomes in Mouse Liver

Y. Umemura, T. Inoue, Tadashi Inoue, M. Takagi
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引用次数: 2

Abstract

The aim of this research was to examine the inhibitory effect of aflatoxin B1, one of the most potent hepatocarcinogen, on the translational step in mouse liver. It has been shown that polysomes were released in vitro from microsomal membrane prepared from rat liver by incubation with aflatoxin B1 and that this release of ribosomes was prevented by addition of corticosterone in the incubation medium. In this paper, the same phenomenon was proved to occur in vivo by an improved fractionation methods, in which ribosome-distributions can be analyzed quantitatively, not only between free and membrane-bound states but also between monosomes and polysomes. Administration of aflatoxin B1 to mice induced reductions of membrane-bound ribosomes and polysomes, with concomitant increases of free ribosomes and monosomes in liver. Simultaneous administration of corticosterone prevented this alteration of ribosome-distributions. From these results, it was deduced that a release of polysomes from membrane occurred primarily by administrating aflatoxin, which then caused a shortening of half-life of mRNA on polysomes, resulting in an increase of the amount of monosomes.
黄曲霉毒素B1和皮质酮对小鼠肝脏游离态和膜结合态及单体和多体核糖体分布的影响
本研究的目的是研究黄曲霉毒素B1对小鼠肝脏转化过程的抑制作用,黄曲霉毒素B1是最有效的肝癌原之一。研究表明,用黄曲霉毒素B1孵育大鼠肝脏制备的微粒体膜在体外释放多体,而在孵育培养基中添加皮质酮可阻止核糖体的释放。在本文中,通过改进的分离方法证明了同样的现象在体内也会发生,该方法不仅可以定量分析游离状态和膜结合状态之间的核糖体分布,还可以定量分析单体和多体之间的核糖体分布。给小鼠黄曲霉毒素B1可导致肝内膜结合核糖体和多体减少,同时增加游离核糖体和单体。同时给予皮质酮可防止核糖体分布的这种改变。从这些结果推断,多体从膜上的释放主要是通过施用黄曲霉毒素,然后引起多体上mRNA半衰期的缩短,导致单体数量的增加。
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