PPARγ in Kidney Physiology and Pathophysiology

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Abstract
Involvement of the nuclear receptor peroxisome proliferator‐activated receptor gamma (PPARγ) in kidney physiology has been explored recently. Synthetic PPARγ ligands can ameliorate the diabetic kidney disease through different mechanisms, involving inhibition of mesangial cell growth, reduction of mesangial matrix, and cytokine production of glomerular cells as well as promoting endothelial cell survival within the kidney glomeruli. Activation of PPARγ has additional profibrotic consequences, which can contribute to wound healing in diabetic glomerulonephritis. Beside many beneficial effects, PPARγ activation, however, can lead to severe water retention, a common side effect of thiazolidinedione therapy. This unwanted effect is due to the activation of PPARγ in the mesonephric distal collecting system, where PPARγ positively regulates sodium and water resorbtion leading to the expansion of interstitial fluid volume. Recent studies indicate that PPARγ is also involved in the normal kidney development, renal lipid metabolism, and activation of the renin‐angiotensin system. In this paper, we give a synopsis of the current knowledge on PPARγ functions in kidney phyisology and pathophysiology.
Funding Information
  • Hungarian Scientific Research Fund (76091)

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