Accumulation of uremic solutes in the cerebrospinal fluid in experimental acute renal failure

Am J Physiol Renal Physiol. 2019 Aug 1;317(2):F296-F302. doi: 10.1152/ajprenal.00100.2019. Epub 2019 May 29.

Abstract

The accumulation of uremic solutes in kidney failure may impair mental function. The present study profiled the accumulation of uremic solutes in the cerebrospinal fluid (CSF) in acute renal failure. CSF and plasma ultrafiltrate were obtained from rats at 48 h after sham operation (control; n = 10) or bilateral nephrectomy (n = 10) and analyzed using an established metabolomic platform. Two hundred forty-eight solutes were identified as uremic based on their accumulation in the plasma ultrafiltrate of nephrectomized compared with control rats. CSF levels of 124 of these solutes were sufficient to allow calculation of CSF-to-plasma ultrafiltrate concentration ratios. Levels of many of the uremic solutes were normally lower in the CSF than in the plasma ultrafiltrate, indicating exclusion of these solutes from the brain. CSF levels of the great majority of the uremic solutes increased in renal failure. The increase in the CSF was, however, relatively less than in the plasma ultrafiltrate for most solutes. In particular, for the 31 uremic solutes with CSF-to-plasma ultrafiltrate ratios of <0.25 in control rats, the average CSF-to-plasma ultrafiltrate ratio decreased from 0.13 ± 0.07 in control rats to 0.09 ± 0.06 in nephrectomized rats, revealing sustained ability to exclude these solutes from the brain. In summary, levels of many uremic solutes are normally kept lower in the CSF than in the plasma ultrafiltrate by the action of the blood-brain and blood-CSF barriers. These barriers remain functional but cannot prevent accumulation of uremic solutes in the CSF when the kidneys fail.

Keywords: brain; cerebrospinal fluid; end-stage renal disease; uremic encephalopathy; uremic toxins.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acute Kidney Injury / blood
  • Acute Kidney Injury / cerebrospinal fluid*
  • Acute Kidney Injury / complications
  • Acute Kidney Injury / physiopathology
  • Animals
  • Biomarkers / blood
  • Blood-Brain Barrier / metabolism
  • Blood-Brain Barrier / physiopathology
  • Brain Diseases / blood
  • Brain Diseases / cerebrospinal fluid*
  • Brain Diseases / etiology
  • Brain Diseases / physiopathology
  • Chromatography, High Pressure Liquid
  • Disease Models, Animal
  • Disease Progression
  • Kidney / metabolism
  • Kidney / physiopathology
  • Male
  • Metabolomics / methods
  • Nephrectomy
  • Rats, Sprague-Dawley
  • Spectrometry, Mass, Electrospray Ionization
  • Tandem Mass Spectrometry
  • Uremia / blood
  • Uremia / cerebrospinal fluid*
  • Uremia / etiology
  • Uremia / physiopathology

Substances

  • Biomarkers