Poly(Adenosine 5'-diphosphate-ribose) polymerase inhibition counteracts multiple manifestations of experimental type

Viktor R Drel1, Weizheng Xu, Jie Zhang

  • 1Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana 70808, USA. obrosoig@pbrc.edu

Endocrinology
|October 27, 2009
PubMed

Insights

Poly(ADP-ribose) polymerase (PARP) plays a role in early diabetic nephropathy. Inhibiting PARP in diabetic rats prevented kidney damage and reduced markers of disease progression, suggesting therapeutic potential.

Area of Science:

  • Biochemistry
  • Nephrology
  • Pharmacology

Background:

  • Type 1 diabetes is associated with early-onset nephropathy.
  • Poly(ADP-ribose) polymerase (PARP) activation is implicated in cellular stress and damage.

Purpose of the Study:

  • To evaluate the role of PARP in the development of early nephropathy in type 1 diabetes.
  • To assess the therapeutic potential of PARP inhibitors in diabetic kidney disease.

Main Methods:

  • Streptozotocin-induced diabetic rats were treated with PARP inhibitors (ISO and GPI-15427).
  • PARP activity, markers of kidney damage (albuminuria, TGF-β1, VEGF, ET-1, TNF-α, MCP-1), oxidative stress, and structural changes were assessed.

Main Results:

  • PARP inhibition prevented increased urinary albumin excretion and reduced markers of inflammation and oxidative stress in diabetic rats.
  • PARP inhibitors counteracted diabetes-induced increases in renal TGF-β1, VEGF, ET-1, TNF-α, MCP-1, lipid peroxidation, and nitrotyrosine.
  • Inhibition of PARP also prevented podocyte loss and accumulation of collagen, fibronectin, and advanced glycation end-products in the renal cortex.

Conclusions:

  • PARP activation is a key factor in the pathogenesis of early diabetic nephropathy.
  • PARP inhibitors demonstrate significant renoprotective effects in experimental type 1 diabetes.
  • These findings support the development of PARP inhibitors for treating diabetic kidney disease.

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