Neuron specific metabolic adaptations following multi-day exposures to oxygen glucose deprivation

Biochim Biophys Acta. 2010 Nov;1802(11):1095-104. doi: 10.1016/j.bbadis.2010.07.013. Epub 2010 Jul 23.

Abstract

Prior exposure to sub toxic insults can induce a powerful endogenous neuroprotective program known as ischemic preconditioning. Current models typically rely on a single stress episode to induce neuroprotection whereas the clinical reality is that patients may experience multiple transient ischemic attacks (TIAs) prior to suffering a stroke. We sought to develop a neuron-enriched preconditioning model using multiple oxygen glucose deprivation (OGD) episodes to assess the endogenous protective mechanisms neurons implement at the metabolic and cellular level. We found that neurons exposed to a five minute period of glucose deprivation recovered oxygen utilization and lactate production using novel microphysiometry techniques. Using the non-toxic and energetically favorable five minute exposure, we developed a preconditioning paradigm where neurons are exposed to this brief OGD for three consecutive days. These cells experienced a 45% greater survival following an otherwise lethal event and exhibited a longer lasting window of protection in comparison to our previous in vitro preconditioning model using a single stress. As in other models, preconditioned cells exhibited mild caspase activation, an increase in oxidized proteins and a requirement for reactive oxygen species for neuroprotection. Heat shock protein 70 was upregulated during preconditioning, yet the majority of this protein was released extracellularly. We believe coupling this neuron-enriched multi-day model with microphysiometry will allow us to assess neuronal specific real-time metabolic adaptations necessary for preconditioning.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adaptation, Physiological*
  • Animals
  • Blotting, Western
  • Caspase 3 / metabolism
  • Cell Hypoxia
  • Cells, Cultured
  • Energy Metabolism / drug effects
  • Enzyme Activation / drug effects
  • Glucose / metabolism*
  • Glucose / pharmacology
  • HSP70 Heat-Shock Proteins / metabolism
  • Immunohistochemistry
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Oxygen / metabolism*
  • Oxygen / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Stress, Physiological
  • Time Factors

Substances

  • HSP70 Heat-Shock Proteins
  • Reactive Oxygen Species
  • Caspase 3
  • Glucose
  • Oxygen