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大鼠体内的铜中毒与耐受性。I——肝脏和肾脏铜含量的变化。

Copper toxicosis and tolerance in the rat. I--Changes in copper content of the liver and kidney.

作者信息

Haywood S

出版信息

J Pathol. 1985 Feb;145(2):149-58. doi: 10.1002/path.1711450203.

Abstract

Rats can tolerate toxic copper diets; the extent of this adaptation and the changes that take place in the liver and kidney with respect to copper are studied. Rats were fed diets containing 3000-6000 mg/kg copper for 15 weeks and groups were killed at regular intervals. Their livers and kidneys were examined for pathological changes and for their copper content. Liver copper rose rapidly in the 3000 mg/kg trial to 4780 +/- 636 micrograms/g copper between 4 and 5 weeks with marked liver damage. Stainable copper protein was present at 2 weeks in the hepatocytes but had disappeared by 5 weeks. Liver copper subsequently fell with recovery by 15 weeks. Kidney copper rose to plateau from 4 weeks. Stainable copper protein was present from 2 weeks in the cells of the proximal tubules and was apparently excreted. Tubular necrosis occurred at 4-5 weeks followed by regeneration. In the 6000 mg/kg trial the toxicosis was prolonged. Copper toxicosis in the rat can be a temporary phenomenon during the transformation of copper protein synthesis in the liver from a stainable to a non stainable form. Adaptation occurs after the removal of excess liver copper, facilitated probably by renal excretion, and the animals become tolerant.

摘要

大鼠能够耐受含毒铜的饮食;研究了这种适应的程度以及肝脏和肾脏中与铜相关的变化。给大鼠喂食含3000 - 6000毫克/千克铜的饮食15周,并定期处死各组大鼠。检查它们的肝脏和肾脏是否有病理变化以及铜含量。在3000毫克/千克的试验中,肝脏铜在4至5周内迅速升至4780±636微克/克铜,同时伴有明显的肝脏损伤。在2周时,肝细胞中出现可染色的铜蛋白,但在5周时消失。随后肝脏铜随着恢复在15周时下降。肾脏铜从4周开始升至平稳状态。从2周起,近端小管细胞中出现可染色的铜蛋白,且显然被排泄掉。在4至5周时发生肾小管坏死,随后再生。在6000毫克/千克的试验中,中毒情况持续时间更长。大鼠的铜中毒可能是肝脏中铜蛋白合成从可染色形式转变为不可染色形式过程中的一种暂时现象。在多余的肝脏铜被清除后出现适应,这可能是通过肾脏排泄来促进实现的,并且动物变得具有耐受性。

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