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锂诱导的大鼠尿毒症——一种慢性肾衰竭的新模型。

Lithium-induced uremia in rats - a new model of chronic renal failure.

作者信息

Christensen S, Ottosen P D

出版信息

Pflugers Arch. 1983 Nov;399(3):208-12. doi: 10.1007/BF00656716.

Abstract

Three groups of new-born rats were studied: Group Li/Li treated with Li for 16 weeks, group Li/C treated for 8 weeks followed by 8 weeks without Li, and Group C/C 16 weeks old controls. Both Li-treated groups showed severe reduction of renal function, particularly group Li/Li, where the mean GFR was reduced by 80%. Plasma urea, creatinine, and osmolality were increased, blood hemoglobin and hematocrit were reduced, whereas plasma Na, K, and standard bicarbonate were unchanged. Na clearance was maintained and fractional Na excretion thus increased. Fractional Li excretion was also increased, indicating inhibition of proximal tubular salt and water reabsorption. Renal concentrating ability was markedly reduced. When Li was withdrawn, plasma urea levels remained unchanged or continued to rise, and the concentrating defect persisted. The results demonstrate that Li administration to new-born rats causes irreversible chronic renal failure which may progress even in the absence of Li. This model of chronic renal failure has several characteristics in common with chronic renal failure in humans.

摘要

对三组新生大鼠进行了研究

锂/锂组用锂治疗16周,锂/对照(Li/C)组先治疗8周,然后停用锂8周,以及16周龄的对照/对照(C/C)组。两个锂治疗组均显示出严重的肾功能减退,尤其是锂/锂组,其平均肾小球滤过率(GFR)降低了80%。血浆尿素、肌酐和渗透压升高,血血红蛋白和血细胞比容降低,而血浆钠、钾和标准碳酸氢盐未发生变化。钠清除率得以维持,因此钠排泄分数增加。锂排泄分数也增加,表明近端肾小管对盐和水的重吸收受到抑制。肾脏浓缩能力明显降低。停用锂后,血浆尿素水平保持不变或继续升高,浓缩缺陷持续存在。结果表明,给新生大鼠施用锂会导致不可逆的慢性肾衰竭,即使在没有锂的情况下也可能进展。这种慢性肾衰竭模型与人类慢性肾衰竭有几个共同特征。

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