Ability of NAD and Sirt1 to epigenetically suppress albuminuria

Clin Exp Nephrol. 2024 Jul;28(7):599-607. doi: 10.1007/s10157-024-02502-w. Epub 2024 Apr 8.

Abstract

The time for diabetic nephropathy (DN) to progress from mild to severe is long. Thus, methods to continuously repress DN are required to exert long-lasting effects mediated through epigenetic regulation. In this study, we demonstrated the ability of nicotinamide adenine dinucleotide (NAD) and its metabolites to reduce albuminuria through Sirt1- or Nampt-dependent epigenetic regulation. We previously reported that proximal tubular Sirt1 was lowered before glomerular Sirt1. Repressed glomerular Sirt1 was found to epigenetically elevate Claudin-1. In addition, we reported that proximal tubular Nampt deficiency epigenetically augmented TIMP-1 levels in Sirt6-mediated pathways, leading to type-IV collagen deposition and diabetic fibrosis. Altogether, we propose that the Sirt1/Claudin-1 axis may be crucial in the onset of albuminuria at the early stages of DN and that the Nampt/Sirt6/TIMP-1 axis promotes diabetic fibrosis in the middle to late stages of DN. Finally, administration of NMN, an NAD precursor, epigenetically potentiates the regression of the onset of DN to maintain Sirt1 and repress Claudin-1 in podocytes, suggesting the potential use of NAD metabolites as epigenetic medications for DN.

Keywords: Claudin-1; Nicotinamide mononucleotide; Sirtuin 1.

Publication types

  • Review

MeSH terms

  • Albuminuria* / genetics
  • Animals
  • Claudin-1* / genetics
  • Claudin-1* / metabolism
  • Cytokines / metabolism
  • Diabetic Nephropathies* / genetics
  • Diabetic Nephropathies* / metabolism
  • Epigenesis, Genetic*
  • Fibrosis
  • Humans
  • Kidney Tubules, Proximal / drug effects
  • Kidney Tubules, Proximal / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NAD* / metabolism
  • Nicotinamide Mononucleotide / pharmacology
  • Nicotinamide Phosphoribosyltransferase / genetics
  • Nicotinamide Phosphoribosyltransferase / metabolism
  • Podocytes / metabolism
  • Sirtuin 1* / genetics
  • Sirtuin 1* / metabolism
  • Sirtuins / genetics
  • Sirtuins / metabolism
  • Tissue Inhibitor of Metalloproteinase-1* / genetics
  • Tissue Inhibitor of Metalloproteinase-1* / metabolism

Substances

  • Claudin-1
  • Cytokines
  • NAD
  • Nicotinamide Mononucleotide
  • Nicotinamide Phosphoribosyltransferase
  • nicotinamide phosphoribosyltransferase, mouse
  • Sirt1 protein, mouse
  • Sirt6 protein, mouse
  • Sirtuin 1
  • Sirtuins
  • Timp1 protein, mouse
  • Tissue Inhibitor of Metalloproteinase-1