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长期镉暴露通过降低大鼠肾脏中促红细胞生成素的水平诱导大鼠贫血。

Long-term cadmium exposure induces anemia in rats through hypoinduction of erythropoietin in the kidneys.

作者信息

Horiguchi H, Sato M, Konno N, Fukushima M

机构信息

Department of Public Health, Fukushima Medical College, Japan.

出版信息

Arch Toxicol. 1996;71(1-2):11-9. doi: 10.1007/s002040050352.

Abstract

Cadmium (Cd), a highly toxic heavy metal, is distributed widely in the general environment of today. The characteristic clinical manifestations of chronic Cd intoxication include renal proximal tubular dysfunction, general osteomalacia with severe pains, and anemia. We have recently reported that the serum level of erythropoietin (EPO) remained low despite the severe anemia in patients with Itai-itai disease, the most severe form of chronic Cd intoxication. In order to prove that the anemia observed in chronic Cd intoxication arises from low production of EPO in the kidneys following the renal injury, we administered Cd to rats for a long period and performed the analysis of EPO mRNA inducibility in the kidneys. The rats administered Cd for 6 and 9 months showed anemia with low levels of plasma EPO as well as biochemical and histological renal tubular damage, and also hypoinduction of EPO mRNA in the kidneys. The results indicate that chronic Cd intoxication causes anemia by disturbing the EPO-production capacity of renal cells.

摘要

镉(Cd)是一种剧毒重金属,在当今的一般环境中广泛分布。慢性镉中毒的典型临床表现包括肾近端小管功能障碍、伴有剧痛的全身性骨软化症以及贫血。我们最近报道,尽管痛痛病(最严重的慢性镉中毒形式)患者存在严重贫血,但其促红细胞生成素(EPO)的血清水平仍较低。为了证明慢性镉中毒时观察到的贫血是由于肾损伤后肾脏中EPO生成减少所致,我们长期给大鼠施用镉,并对肾脏中EPO mRNA的诱导能力进行了分析。施用镉6个月和9个月的大鼠出现贫血,血浆EPO水平较低,同时伴有肾小管的生化和组织学损伤,并且肾脏中EPO mRNA的诱导不足。结果表明,慢性镉中毒通过干扰肾细胞的EPO生成能力而导致贫血。

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