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蛋白结合型尿毒症毒素:心肾综合征中一个长期被忽视的罪魁祸首。

Protein-bound uremic toxins: a long overlooked culprit in cardiorenal syndrome.

作者信息

Lekawanvijit Suree, Kompa Andrew R, Krum Henry

机构信息

Department of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand; and

Centre of Cardiovascular Research and Education in Therapeutics, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.

出版信息

Am J Physiol Renal Physiol. 2016 Jul 1;311(1):F52-62. doi: 10.1152/ajprenal.00348.2015. Epub 2016 May 4.

Abstract

Protein-bound uremic toxins (PBUTs) accumulate once renal excretory function declines and are not cleared by dialysis. There is increasing evidence that PBUTs exert toxic effects on many vital organs, including the kidney, blood vessels, and heart. It has been suggested that PBUTs are likely to be a potential missing link in cardiorenal syndrome, based on the high incidence of cardiovascular events and mortality in the dialysis population, which are dramatically reduced in successful kidney transplant recipients. These data have led the call for more effective dialysis or additional adjunctive therapy to eradicate these toxins and their adverse biological effects. Indoxyl sulfate and p-cresyl sulfate are the two most problematic PBUTs, conferring renal and cardiovascular toxicity, and are derived from dietary amino acid metabolites by colonic microbial organisms. Therefore, targeting the colon where these toxins are initially produced appears to be a potential therapeutic alternative for patients with chronic kidney disease. This strategy, if approved, is likely to be applicable to predialysis patients, thereby potentially preventing progression of chronic kidney disease to end-stage renal disease as well as preventing the development of cardiorenal syndrome.

摘要

随着肾功能衰退,蛋白结合型尿毒症毒素(PBUTs)会蓄积,且无法通过透析清除。越来越多的证据表明,PBUTs会对包括肾脏、血管和心脏在内的许多重要器官产生毒性作用。鉴于透析人群中心血管事件和死亡率的高发生率,而在成功接受肾移植的受者中这些情况会显著降低,有人提出PBUTs可能是心肾综合征中一个潜在的缺失环节。这些数据促使人们呼吁采用更有效的透析或额外的辅助治疗来清除这些毒素及其不良生物学效应。硫酸吲哚酚和对甲酚硫酸酯是两个最成问题的PBUTs,具有肾脏和心血管毒性,它们由结肠微生物从膳食氨基酸代谢产物中产生。因此,针对这些毒素最初产生的结肠进行干预,似乎是慢性肾脏病患者的一种潜在治疗选择。如果该策略获得批准,可能适用于透析前患者,从而有可能预防慢性肾脏病进展至终末期肾病,以及预防心肾综合征的发生。

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