Pathophysiology and therapeutics of premature ageing in chronic kidney disease, with a focus on glycative stress

Clin Exp Pharmacol Physiol. 2017 Dec:44 Suppl 1:70-77. doi: 10.1111/1440-1681.12777. Epub 2017 Sep 20.

Abstract

Chronic kidney disease (CKD) is a major concern in public health. The pathology of CKD includes premature ageing in the kidney and vessels, which results in a high risk of cardiovascular events and end-stage renal disease. Many factors are involved in premature ageing in CKD, including hormonal imbalance, glycative stress, nitrogenous metabolites, and oxidative stress. Of these, the most important role in premature ageing in CKD is played by glycative stress, namely a massive and unfavourable glycation state, since the kidney is responsible for the clearance of advanced glycation endproducts (AGEs). In an animal model, overexpression of glyoxalase I (GLO-1), a detoxifier of AGEs, has been found to alleviate premature ageing in the kidney and vessels. Both lifestyle changes and drug therapy have shown promise in overcoming premature ageing. Promising drug therapies include a GLO-1 activator and an absorbent against glycotoxin and nitrogenous metabolites.

Keywords: GLO-1; chronic kidney disease; glycative stress; indoxyl sulphate; phosphorus; premature ageing.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging, Premature*
  • Cell Hypoxia
  • Cellular Senescence* / drug effects
  • Enzyme Activation
  • Enzyme Activators / therapeutic use
  • Frailty / metabolism
  • Frailty / physiopathology
  • Glycation End Products, Advanced / metabolism*
  • Health Status
  • Hormones / metabolism
  • Humans
  • Kidney / drug effects
  • Kidney / metabolism*
  • Kidney / pathology
  • Kidney / physiopathology
  • Lactoylglutathione Lyase / metabolism
  • Oxidative Stress
  • Renal Insufficiency, Chronic / diagnosis
  • Renal Insufficiency, Chronic / metabolism*
  • Renal Insufficiency, Chronic / physiopathology
  • Renal Insufficiency, Chronic / therapy
  • Risk Reduction Behavior
  • Signal Transduction
  • Water-Electrolyte Balance

Substances

  • Enzyme Activators
  • Glycation End Products, Advanced
  • Hormones
  • GLO1 protein, human
  • Lactoylglutathione Lyase