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镉硫蛋白与镉对汞肾毒性的保护作用。

Cadmium-thionein and the protection by cadmium against the nephrotoxicity of mercury.

作者信息

Webb M, Magos L

出版信息

Chem Biol Interact. 1976 Aug;14(3-4):357-69. doi: 10.1016/0009-2797(76)90114-9.

Abstract

Uptake of Hg2+ into the renal and hepatic metallothioneins of rats is increased by pretreatment with Cd2+. This increased uptake occurs both by displacement of Cd2+ (and of Zn2+) from the presynthesized cadmium-thionein, and by further synthesis of thionein. The former mechanism predominates in the kidney of the male rat, which is more sensitive than the female to Hg2+. The latter mechanism, which occurs particularly in the kidney of the female, also is considered to involve an initial displacement of Cd2+ from cadmium-thionein, but is followed by further synthesis of the metalloprotein, which is induced by the liberated cation. Pretreatment with Cd2+ increases not only the incorporation of Hg2+ into the renal metallothionein, but also the uptake of Hg2+ into other components of the kidney. At dose levels of Hg2+ at which Cd2+-pretreatment gives complete protection against the nephrotoxicity in male and female rats, the increase in Hg2+-uptake into both the particulate components and into the soluble fraction of the kidney is greater than into metallothionein. It is concluded, therefore, that binding of Hg2+ by pre-induced cadmium-thionein alone cannot explain the protection by Cd2+ against the nephrotoxicity of Hg2+.

摘要

用Cd2+预处理可增加大鼠肾和肝金属硫蛋白对Hg2+的摄取。这种摄取增加既通过从预先合成的镉硫蛋白中置换出Cd2+(以及Zn2+),也通过硫蛋白的进一步合成来实现。前一种机制在雄性大鼠肾脏中占主导,雄性大鼠对Hg2+比雌性更敏感。后一种机制尤其发生在雌性大鼠肾脏中,也被认为涉及从镉硫蛋白中最初置换出Cd2+,但随后是金属蛋白的进一步合成,这是由释放的阳离子诱导的。用Cd2+预处理不仅增加了Hg2+掺入肾金属硫蛋白,还增加了Hg2+进入肾脏其他成分的摄取。在Cd2+预处理能完全保护雄性和雌性大鼠免受Hg2+肾毒性的Hg2+剂量水平下,Hg2+进入肾脏颗粒成分和可溶性部分的摄取增加量大于进入金属硫蛋白的增加量。因此得出结论,仅靠预先诱导的镉硫蛋白结合Hg2+不能解释Cd2+对Hg2+肾毒性的保护作用。

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