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滤过蛋白的肾小管毒性。

Tubular toxicity of filtered proteins.

作者信息

Ledingham J G

机构信息

Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Headington, UK.

出版信息

Am J Nephrol. 1990;10 Suppl 1:52-7. doi: 10.1159/000168194.

Abstract

The mechanisms by which low-molecular-weight proteins filtered at the glomerulus might damage the kidney are reviewed. Despite a strong association between Bence-Jones proteinuria and impairment of renal function, many patients excrete light chains in large amounts and for long periods without evidence of renal abnormality. This critical paradox has still not been resolved despite suggestions, and investigations to explore them, that physicochemical properties of individual proteins might determine toxicity. The data suggest contributions, not mutually exclusive, from toxicity to proximal tubular cells via lysosomal uptake and from tubular obstruction by casts containing light chain and Tamm-Horsfall protein. The mechanisms, if any, of nephrotoxicity of haem proteins are equally uncertain.

摘要

本文综述了肾小球滤过的低分子量蛋白质可能损害肾脏的机制。尽管本-周蛋白尿与肾功能损害之间存在密切关联,但许多患者长期大量排泄轻链却无肾脏异常证据。尽管有人提出并进行了相关研究,认为单个蛋白质的物理化学性质可能决定毒性,但这一关键悖论仍未得到解决。数据表明,通过溶酶体摄取对近端肾小管细胞产生毒性以及由含有轻链和Tamm-Horsfall蛋白的管型导致肾小管梗阻,这两种机制并非相互排斥,都对肾脏损害有作用。血红素蛋白的肾毒性机制(如果存在的话)同样不明确。

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