大鼠体内镉与植物螯合素结合的命运。

Y Fujita, H I el Belbasi, K S Min, S Onosaka, Y Okada, Y Matsumoto, N Mutoh, K Tanaka
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引用次数: 0

摘要

利用合成的109Cd-PC,研究了大鼠体内镉(Cd)与植物螯合素[PC, (γ - glu - cys)n-Gly)]的结合情况。通过消化道吸收的Cd比CdCl2少,但肾Cd与肝Cd的比值较高。经肠外给药Cd- pc后,Cd主要分布于肝脏、肾脏、小肠和胰腺。Cd- pc给药后肾脏中Cd含量高于肝脏(n = 5)。给药0.5小时后,大部分Cd结合到肝细胞质中的高分子量部分,并在6小时后转移到金属硫蛋白部分。即使在Cd注射后或前3小时给予游离PC (n = 5),也不影响Cd的组织分布。仅在同时给药Cd和PC的情况下,其在肾脏中的分布增加。这些结果表明,虽然吸收的Cd比CdCl2更多地分布到肾脏,但与PC结合的Cd从消化道的吸收比CdCl2低,并且Cd在被细胞摄取后很快从PC中释放出来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fate of cadmium bound to phytochelatin in rats.

The fate cadmium(Cd) bound to phytochelatin [PC, (gamma-Glu-Cys)n-Gly)] was studied in rats using synthesized 109Cd-PC. Less Cd was absorbed through the digestive tracts than CdCl2, but the ratio of renal Cd to hepatic Cd was higher. After parenteral administration of Cd-PC, Cd was distributed mainly in the liver, kidney, small intestine and pancreas. More Cd was found in the kidney than the liver after Cd-PC (n = 5) administration. Most of the Cd was bound to the high molecular weight fraction in the hepatic cytosol 0.5 hr after administration and moved to the metallothionein fraction at 6 hr. The tissue distribution of Cd was not affected even when free PC (n = 5) was administered 3 hr after or before Cd injection. The distribution in the kidney increased only in the case of the simultaneous administration of Cd with PC. These findings show that the absorbance of Cd bound to PC from the alimentary tract is lower than that of CdCl2 although absorbed Cd is distributed to the kidney more than CdCl2, and Cd is liberated from PC soon after uptake by the cells.

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