Role of AMPK pathway in lead-induced endoplasmic reticulum stress in kidney and in paeonol-induced protection in mice

Food Chem Toxicol. 2018 Dec:122:87-94. doi: 10.1016/j.fct.2018.10.024. Epub 2018 Oct 6.

Abstract

Paeonol is a natural flavonoid isolated from Moutan Cortex, which has been found to exhibit antioxidant, anti-apoptotic, anti-aging and anti-inflammatory bioactivities. Herein, we investigated the nephroprotective efficacy of paeonol against Pb-induced toxicity and elucidated the potential mechanisms. The results revealed that paeonol significantly ameliorated renal dysfunction and histology changes of Pb-treated mice. Paeonol inhibited oxidative stress and increased activities of antioxidant enzyme in the kidneys of Pb-treated mice. Paeonol decreased the nuclear factor-κB activation and over-production of inflammatory cytokines tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). Paeonol suppressed endoplasmic reticulum (ER) stress in kidneys of in the Pb treatment group and primary kidney mesangial cells. Moreover, paeonol increased the denosine 5'-monophosphate-activated protein kinase (AMPK) phosphorylation and decreased the activations of glycogen synthase kinase-3 (GSK-3), protein kinase RNA-like ER kinase (PERK), inositol-requiring protein-1 (IRE1), c-jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK). These results were further confirmed in primary kidney mesangial cells. Taken together, these findings indicate that paeonol could protect kidney form Pb-induced injury by inhibiting oxidative stress, ER stress and inflammation via the AMPK and GSK-3 pathway. Paeonol might be a potential therapeutic agent to inhibit ER stress-associated inflammation in lead-stimulated kidneys.

Keywords: AMPK; ER stress; Inflammation; Lead; Oxidative stress; Paeonol.

MeSH terms

  • Acetophenones / pharmacology*
  • Adenylate Kinase / metabolism*
  • Animals
  • Cells, Cultured
  • Drugs, Chinese Herbal / chemistry
  • Endoplasmic Reticulum Stress / drug effects*
  • Enzyme Activation
  • Glomerular Mesangium / drug effects*
  • Glomerular Mesangium / enzymology*
  • Glomerular Mesangium / metabolism
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Inflammation / prevention & control
  • Inflammation Mediators / metabolism
  • Interleukin-6 / biosynthesis
  • Lead / toxicity*
  • MAP Kinase Kinase 4 / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Mice, Inbred ICR
  • NF-kappa B / metabolism
  • Oxidative Stress / drug effects
  • Paeonia / chemistry
  • Protein Serine-Threonine Kinases / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis
  • eIF-2 Kinase / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Acetophenones
  • Drugs, Chinese Herbal
  • Inflammation Mediators
  • Interleukin-6
  • Membrane Proteins
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse
  • moutan cortex
  • Lead
  • paeonol
  • Ern2 protein, mouse
  • Glycogen Synthase Kinase 3 beta
  • Gsk3b protein, mouse
  • PERK kinase
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase
  • p38 Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Adenylate Kinase