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孤立功能肾代偿性适应的生理学与病理生理学

Physiology and Pathophysiology of Compensatory Adaptations of a Solitary Functioning Kidney.

作者信息

McArdle Zoe, Schreuder Michiel F, Moritz Karen M, Denton Kate M, Singh Reetu R

机构信息

Cardiovascular Program, Monash Biomedicine Discovery Institute and Department of Physiology, Monash University, Melbourne, VIC, Australia.

Department of Pediatric Nephrology, Amalia Children's Hospital, Radboud University Medical Center, Nijmegen, Netherlands.

出版信息

Front Physiol. 2020 Jun 26;11:725. doi: 10.3389/fphys.2020.00725. eCollection 2020.

Abstract

Children born with a solitary functioning kidney (SFK) have an increased risk of hypertension and kidney disease from early in adulthood. In response to a reduction in kidney mass, the remaining kidney undergoes compensatory kidney growth. This is associated with both an increase in size of the kidney tubules and the glomeruli and an increase in single nephron glomerular filtration rate (SNGFR). The compensatory hypertrophy and increase in filtration at the level of the individual nephron results in normalization of total glomerular filtration rate (GFR). However, over time these same compensatory mechanisms may contribute to kidney injury and hypertension. Indeed, approximately 50% of children born with a SFK develop hypertension by the age of 18 and 20-40% require dialysis by the age of 30. The mechanisms that result in kidney injury are only partly understood, and early biomarkers that distinguish those at an elevated risk of kidney injury are needed. This review will outline the compensatory adaptations to a SFK, and outline how these adaptations may contribute to kidney injury and hypertension later in life. These will be based largely on the mechanisms we have identified from our studies in an ovine model of SFK, that implicate the renal nitric oxide system, the renin angiotensin system and the renal nerves to kidney disease and hypertension associated with SFK. This discussion will also evaluate current, and speculate on next generation, prognostic factors that may predict those children at a higher risk of future kidney disease and hypertension.

摘要

出生时仅有一个功能肾(SFK)的儿童在成年早期患高血压和肾脏疾病的风险会增加。作为对肾单位数量减少的一种反应,剩余的肾脏会经历代偿性肾生长。这与肾小管和肾小球的增大以及单个肾单位肾小球滤过率(SNGFR)的增加都有关联。单个肾单位水平上的代偿性肥大和滤过增加会使总肾小球滤过率(GFR)恢复正常。然而,随着时间的推移,这些相同的代偿机制可能会导致肾脏损伤和高血压。事实上,大约50%出生时患有SFK的儿童在18岁时会患上高血压,20 - 40%的人在30岁时需要透析。导致肾脏损伤的机制仅部分为人所知,因此需要早期生物标志物来区分那些肾脏损伤风险升高的人。本综述将概述对SFK的代偿性适应,并阐述这些适应如何在以后的生活中导致肾脏损伤和高血压。这些将主要基于我们在SFK绵羊模型研究中所确定的机制,这些机制表明肾一氧化氮系统、肾素 - 血管紧张素系统和肾神经与SFK相关的肾脏疾病和高血压有关。本讨论还将评估当前的,并推测下一代可能预测那些未来患肾脏疾病和高血压风险较高儿童的预后因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f54c/7332829/c45a401b5cc7/fphys-11-00725-g001.jpg

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