PGC-1α ameliorates kidney fibrosis in mice with diabetic kidney disease through an antioxidative mechanism

Mol Med Rep. 2018 Mar;17(3):4490-4498. doi: 10.3892/mmr.2018.8433. Epub 2018 Jan 16.

Abstract

The production of reactive oxygen species (ROS) is a common phenomenon in podocyte impairment, which leads to the irreversible progression of chronic kidney diseases, such as diabetic kidney disease (DKD). Previous research has indicated that peroxisome proliferator‑activated receptor γ (PPARγ) coactivator‑1α (PGC‑1α) participates in mitochondrial biogenesis and energy metabolism in certain mitochondria‑enriched cells, including myocardial and skeletal muscle cells. Therefore, we hypothesized that PGC‑1α may be a protective nuclear factor against energy and oxidative stress in DKD. To investigate this hypothesis, db/db diabetic mice were used to establish a DKD model and the PPARγ agonist rosiglitazone was employed to induce PGC‑1α expression in vivo. Additionally, immortalized mouse podocytes and SV40 MES 13 renal mesangial cells were utilized for in vitro experiments. The expression levels of PGC‑1α and genes associated with kidney and cell injury were determined by western blotting or reverse transcription-quantitative polymerase chain reaction and intracellular ROS levels were assessed by 2',7'-dichlorodihydrofluorescein diacetate. The results of the present study demonstrated that endogenous PGC‑1α expression exhibited protective effects against oxidative stress, glomerulosclerosis and tubulointerstitial fibrosis in experimental DKD. These results indicated a potential role of PGC‑1α in the amelioration of key pathophysiological features of DKD and provided evidence for PGC‑1α as a potential therapeutic target in DKD.

Keywords: peroxisome proliferator-activated receptor γ coactivator-1α; diabetic kidney disease; oxidative damage.

MeSH terms

  • Animals
  • Cell Line
  • Diabetic Nephropathies / etiology
  • Diabetic Nephropathies / pathology*
  • Diabetic Nephropathies / veterinary
  • Fibrosis
  • Kidney / metabolism
  • Kidney / pathology*
  • Mesangial Cells / cytology
  • Mesangial Cells / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Nuclear Respiratory Factor 1 / genetics
  • Nuclear Respiratory Factor 1 / metabolism
  • PPAR gamma / agonists
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / antagonists & inhibitors
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism*
  • Podocytes / cytology
  • Podocytes / metabolism
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Reactive Oxygen Species / metabolism
  • Rosiglitazone
  • Serum Albumin / analysis
  • Superoxide Dismutase / metabolism
  • Thiazolidinediones / pharmacology
  • Up-Regulation / drug effects

Substances

  • Nrf1 protein, mouse
  • Nuclear Respiratory Factor 1
  • PPAR gamma
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Serum Albumin
  • Thiazolidinediones
  • Rosiglitazone
  • Superoxide Dismutase