Dehydroascorbic acid-induced endoplasmic reticulum stress and leptin resistance in neuronal cells

Biochem Biophys Res Commun. 2016 Sep 16;478(2):716-20. doi: 10.1016/j.bbrc.2016.08.013. Epub 2016 Aug 4.

Abstract

Due to its anti-obesity effects, an adipocyte-derived hormone, leptin, has become important for the treatment of obesity. However, most obese subjects are in a state of leptin resistance, and endoplasmic reticulum (ER) stress is suggested to be involved in the pathophysiology of leptin resistance. Dehydroascorbic acid (DHAA), an oxidized form of vitamin C, was found to be increased in diabetes. In the present study, we investigated the possible effects of DHAA on the activation of ER stress and leptin resistance. A human neuroblastoma cell line, stably transfected with the Ob-Rb leptin receptor (SH-SY5Y-ObRb), was treated with DHAA. We found that DHAA upregulated ER stress-related genes such as GRP78, CHOP, and spliced XBP1. Moreover, leptin-induced STAT3 phosphorylation was hindered by DHAA. These results suggested that increases in the levels of DHAA might be harmful to neurons, contributing to defective leptin-responsive signaling.

Keywords: Dehydroascorbic acid (DHAA); Endoplasmic reticulum (ER) stress; Leptin; Leptin resistance; Unfolded protein response (UPR).

MeSH terms

  • Cell Line, Tumor
  • Dehydroascorbic Acid / pharmacology*
  • Endoplasmic Reticulum / drug effects*
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum Chaperone BiP
  • Endoplasmic Reticulum Stress / drug effects*
  • Gene Expression Regulation
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Humans
  • Leptin / genetics
  • Leptin / metabolism
  • Leptin / pharmacology*
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Oxidation-Reduction
  • Phosphorylation / drug effects
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Transcription Factor CHOP / genetics
  • Transcription Factor CHOP / metabolism
  • Unfolded Protein Response / drug effects
  • X-Box Binding Protein 1 / genetics
  • X-Box Binding Protein 1 / metabolism

Substances

  • DDIT3 protein, human
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Leptin
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • X-Box Binding Protein 1
  • XBP1 protein, human
  • Transcription Factor CHOP
  • Dehydroascorbic Acid