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Localization of mercury in the kidney during experimental acute tubular necrosis studied by the cytochemical Silver Amplification method.

机译:通过细胞化学银放大法研究了急性急性肾小管坏死过程中汞在肾脏中的定位。

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摘要

An intravenous injection of 3.0 mg HgCl2/kg bw was given to Balb/c mice. The concentration of mercury in the red blood cells, serum, and kidney was determined after 5 min, 30 min, 2 h and 24 h by atomic absorption spectrophotometry. The concentration of mercury in the serum showed a maximum after 5 min, and reached a constant low level after 30 min, whereas the concentration of mercury in the red blood cells gradually decreased and reached a similar low level at 24 h. The concentration of mercury in the kidney was greatest after 2 h and was markedly reduced at 24 h. The distribution of mercury in the kidney was followed for up to 17 days by the cytochemical Silver Amplification method applied at the light and electron microscopical levels. Mercury accumulated rapidly, but only in the proximal tubular epithelial cells, preferentially in the S2 and S3 segments. At the subcellular level mercury was only found in endocytic structures, and accumulated in the lysosomes. Very large mercury-containing lysosomes developed in the distal S3 segment. Cell necrosis was severest in the S2 and proximal S3 segments. Regenerated and differentiating epithelial cells in the proximal tubules still showed many mercury-containing lysosomes 17 days after the injection.
机译:向Balb / c小鼠静脉注射3.0 mg HgCl2 / kg bw。通过原子吸收分光光度法测定5分钟,30分钟,2小时和24小时后,红细胞,血清和肾脏中汞的浓度。血清中的汞浓度在5分钟后达到最大值,并在30分钟后达到恒定的低水平,而红细胞中的汞浓度逐渐降低并在24 h达到类似的低水平。肾脏中汞的浓度在2 h后最大,并在24 h时明显降低。通过在光和电子显微镜下应用的细胞化学银放大方法,追踪了汞在肾脏中的分布长达17天。汞迅速积累,但仅在近端肾小管上皮细胞中积累,优先在S2和S3段中积累。在亚细胞水平上,汞仅在胞吞结构中发现,并在溶酶体中积累。在S3远端节段发育了非常大的含汞溶酶体。 S2和S3近端细胞坏死最严重。注射后第17天,近端小管中的再生和分化上皮细胞仍显示出许多含汞溶酶体。

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