Chlorogenic Acid Prevents AMPA-Mediated Excitotoxicity in Optic Nerve Oligodendrocytes Through a PKC and Caspase-Dependent Pathways

Neurotox Res. 2018 Oct;34(3):559-573. doi: 10.1007/s12640-018-9911-5. Epub 2018 Jul 13.

Abstract

In the CNS, including the optic nerve, oligodendrocytes play a critical role in the myelination of axons. Oligodendrocytes are exceptionally sensitive to insults to the CNS, such as injury, ischemia, or inflammation, which result in the loss of oligodendrocytes and myelin and eventually secondary axon degeneration. Oligodendrocytes are sensitive to excitotoxic insults mediated by overactivation of their AMPA ionotropic glutamate receptors. Phenolic compounds, which are widely distributed in fruits and vegetables, received the great attention of scientists due to their antioxidant activities and free radical scavenging abilities. Chlorogenic acid (CGA) has been demonstrated to possess potent neuroprotective activities against oxidative stress in various cellular models and pathological conditions. Hence, CGA protect against oxidative stress and excitotoxic insults mediated by AMPA receptors and that the protective mechanisms involve free radical scavenging, Ca2+ handling in the cytosol, and modulating antioxidant enzyme system. CGA was associated with the protein kinase A (PKC) signaling pathways transduction. Caspases and calpains have been studied as apoptotic mediators and cell death in this model of AMPA toxicity. Inhibitors of caspases initiators, caspases 1, 8, and 9, the upstream of caspase 3 effectors, have totally abrogated the protective activity of CGA. Inhibitors of calpains also totally abrogated the protective activity of CGA. In addition, a potential role for the CGA in inhibiting Bax in oligodendrocyte cell model undergoing AMPA is inducing excitotoxic death. Our results indicate that CGA exhibits a protective potential via antioxidant and apoptosis caspases and calpains dependent against AMPA-mediated excitotoxicity, and these finding indicate that CGA is able to be a good candidate for preventive approach for neurodegenerative disorders associated with loss and damage in oligodendrocytes and AMPA-mediated excitotoxicity.

Keywords: AMPA excitotoxicity; Antioxidant enzymes; Apoptosis pathway; Chlorogenic acid; Oligodendrocyte; PKC; ROS.

MeSH terms

  • Animals
  • Animals, Newborn
  • Caspases / metabolism*
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chlorogenic Acid / pharmacology*
  • Enzyme Inhibitors / pharmacology
  • Excitatory Amino Acid Agonists / toxicity
  • Hydrogen Peroxide / metabolism
  • Iron / metabolism
  • Mitochondria / drug effects
  • Oligodendroglia / drug effects*
  • Optic Nerve / cytology*
  • Protein Kinase C / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects*
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid / toxicity

Substances

  • Enzyme Inhibitors
  • Excitatory Amino Acid Agonists
  • Reactive Oxygen Species
  • Chlorogenic Acid
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • Hydrogen Peroxide
  • Iron
  • Protein Kinase C
  • Caspases