Pathophysiology of Chronic Kidney Disease Progression: Organ and Cellular Considerations

Anupam Agarwal, Karl A. Nath

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Progression of chronic kidney disease (CKD) involves the recruitment and engagement of cellular processes originating in specific compartments of the kidney on the one hand and biochemical pathways of cell injury that contribute to these processes on the other hand. Many of these processes possess the capacity to ramify broadly beyond the compartment where they initially arose. It is this essential consideration that contributes so fundamentally to the increasing loss of functional nephrons and the progression of CKD. A number of different biochemical pathways contribute to CKD progression: angiotensin II induces TGF-β1 and the consequent elaboration of extracellular matrix; angiotensin II also induces oxidative stress which itself can upregulate TGF-β1 in vicinal cells and thus the propagation of a fibrosing response. This lack of containment of compartmental processes, and this versatility of injurious biochemical pathways, not only underlies the pathogenesis of CKD but also holds substantial therapeutic significance. Namely, the best hope for retarding or preventing the progression of CKD resides in a combined, multipronged therapeutic approach that interrupts these processes and pathways at separate and several steps.

Original languageEnglish (US)
Title of host publicationChronic Renal Disease
PublisherElsevier
Pages263-278
Number of pages16
ISBN (Electronic)9780128158760
ISBN (Print)9780128158777
DOIs
StatePublished - Jan 1 2019

Keywords

  • Endothelin
  • Heme oxygenase
  • Injury
  • Kidney compartments
  • Oxidative stress
  • Progression
  • TGF-β1

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Fingerprint

Dive into the research topics of 'Pathophysiology of Chronic Kidney Disease Progression: Organ and Cellular Considerations'. Together they form a unique fingerprint.

Cite this