Blood Thiol Redox State in Chronic Kidney Disease.
Maria Lisa GaravagliaDaniela GiustariniGraziano ColomboFrancesco ReggianiSilvia FinazziMarta CalatroniLucia LandoniNicola Marcello PortinaroAldo MilzaniSalvatore BadalamentiRanieri RossiIsabella Dalle-DonnePublished in: International journal of molecular sciences (2022)
Thiols (sulfhydryl groups) are effective antioxidants that can preserve the correct structure of proteins, and can protect cells and tissues from damage induced by oxidative stress. Abnormal levels of thiols have been measured in the blood of patients with moderate-to-severe chronic kidney disease (CKD) compared to healthy subjects, as well as in end-stage renal disease (ESRD) patients on haemodialysis or peritoneal dialysis. The levels of protein thiols (a measure of the endogenous antioxidant capacity inversely related to protein oxidation) and S -thiolated proteins (mixed disulphides of protein thiols and low molecular mass thiols), and the protein thiolation index (the molar ratio of the S -thiolated proteins to free protein thiols in plasma) have been investigated in the plasma or red blood cells of CKD and ESRD patients as possible biomarkers of oxidative stress. This type of minimally invasive analysis provides valuable information on the redox status of the less-easily accessible tissues and organs, and of the whole organism. This review provides an overview of reversible modifications in protein thiols in the setting of CKD and renal replacement therapy. The evidence suggests that protein thiols, S -thiolated proteins, and the protein thiolation index are promising biomarkers of reversible oxidative stress that could be included in the routine monitoring of CKD and ESRD patients.
Keyphrases
- end stage renal disease
- chronic kidney disease
- peritoneal dialysis
- oxidative stress
- protein protein
- binding protein
- amino acid
- healthcare
- gene expression
- newly diagnosed
- acute kidney injury
- cell proliferation
- signaling pathway
- diabetic rats
- red blood cell
- clinical practice
- early onset
- cell cycle arrest
- heat stress
- high speed
- atomic force microscopy