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窒息的肾脏:终末期肾病中的肾小管间质性缺氧。

The suffocating kidney: tubulointerstitial hypoxia in end-stage renal disease.

机构信息

Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Bunkyo ku, Tokyo, Japan.

出版信息

Nat Rev Nephrol. 2010 Nov;6(11):667-78. doi: 10.1038/nrneph.2010.124. Epub 2010 Sep 28.

Abstract

Chronic kidney disease (CKD) is characterized by irreversible pathological processes that result in the development of end-stage renal disease (ESRD). Accumulating evidence has emphasized the important role of chronic hypoxia in the tubulointerstitium in the final common pathway that leads to development of ESRD. The causes of chronic hypoxia in the tubulointerstitium are multifactorial and include mechanisms such as hemodynamic changes and disturbed oxygen metabolism of resident kidney cells. Epidemiological studies have revealed an association between CKD and systemically hypoxic conditions, such as chronic obstructive pulmonary disease and sleep apnea syndrome. In addition to tubulointerstitial hypoxia, glomerular hypoxia can occur and is a crucial factor in the development of glomerular disorders. Chemical compounds, polarographic sensors, and radiographical methods can be used to detect hypoxia. Therapeutic approaches that target chronic hypoxia in the kidney should be effective against a broad range of kidney diseases. Amelioration of hypoxia is one mechanism of inhibiting the renin-angiotensin system, the current gold standard of CKD therapy. Future therapeutic approaches include protection of the vascular endothelium and appropriate activation of hypoxia-inducible factor, a key transcription factor involved in adaptive responses against hypoxia.

摘要

慢性肾脏病(CKD)的特征为不可逆转的病理过程,导致终末期肾病(ESRD)的发生。越来越多的证据强调了慢性缺氧在肾小管间质中的重要作用,它是导致 ESRD 发生的共同途径。肾小管间质慢性缺氧的原因是多因素的,包括血流动力学改变和固有肾细胞氧代谢紊乱等机制。流行病学研究表明,CKD 与慢性阻塞性肺疾病和睡眠呼吸暂停综合征等系统性低氧状态之间存在关联。除了肾小管间质缺氧外,还会发生肾小球缺氧,这是肾小球疾病发展的关键因素。可以使用化学化合物、极谱传感器和放射方法来检测缺氧。针对肾脏慢性缺氧的治疗方法应该对广泛的肾脏疾病有效。改善缺氧是抑制肾素-血管紧张素系统的机制之一,该系统是 CKD 治疗的当前金标准。未来的治疗方法包括保护血管内皮和适当激活缺氧诱导因子,这是一种涉及对缺氧适应性反应的关键转录因子。

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