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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
Abstract:
This study was aimed at evaluating the role for poly(ADP-ribose) polymerase (PARP) in early nephropathy associated with type 1 diabetes. Control and streptozotocin-diabetic rats were maintained with or without treatment with one of two structurally unrelated PARP inhibitors, 1,5-isoquinolinediol (ISO) and 10-(4-methyl-piperazin-1-ylmethyl)-2H-7-oxa-1,2-diaza-benzo[de] anthracen-3-one (GPI-15427), at 3 mg/kg(-1) x d(-1) ip and 30 mg/kg(-1) x d(-1), respectively, for 10 wk after the first 2 wk without treatment. PARP activity in the renal cortex was assessed by immunohistochemistry and Western blot analysis of poly(ADP-ribosyl)ated proteins. Variables of diabetic nephropathy in urine and renal cortex were evaluated by ELISA, Western blot analysis, immunohistochemistry, and colorimetry. Urinary albumin excretion was increased about 4-fold in diabetic rats, and this increase was prevented by ISO and GPI-15427. PARP inhibition counteracted diabetes-associated increase in poly(ADP-ribose) immunoreactivities in renal glomeruli and tubuli and poly(ADP-ribosyl)ated protein level. Renal concentrations of TGF-beta(1), vascular endothelial growth factor, endothelin-1, TNF-alpha, monocyte chemoattractant protein-1, lipid peroxidation products, and nitrotyrosine were increased in diabetic rats, and all these changes as well as an increase in urinary TNF-alpha excretion were completely or partially prevented by ISO and GPI-15427. PARP inhibition counteracted diabetes-induced up-regulation of endothelin (B) receptor, podocyte loss, accumulation of collagen-alpha1 (IY), periodic acid-Schiff-positive substances, fibronectin, and advanced glycation end-products in the renal cortex. In conclusion, PARP activation is implicated in multiple changes characteristic for early nephropathy associated with type 1 diabetes. These findings provide rationale for development and further studies of PARP inhibitors and PARP inhibitor-containing combination therapies.
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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