Metabolic injury in a variable rat model of post-status epilepticus

Epilepsia. 2016 Dec;57(12):1978-1986. doi: 10.1111/epi.13588. Epub 2016 Nov 7.

Abstract

Objective: In vivo studies of epilepsy typically use prolonged status epilepticus to generate recurrent seizures. However, reports on variable status duration have found discrete differences in injury after 40-50 min of seizures, suggesting a pathophysiologic sensitivity to seizure duration. In this report we take a multivariate cluster analysis to study a short duration status epilepticus model using in vivo 7T magnetic resonance spectroscopy (MRS) and histologic evaluation.

Methods: The Hellier Dudek model was applied with 45 min of status epilepticus after which the animals were imaged twice, at 3 days and 3 weeks post-status epilepticus. Single voxel point resolved spectroscopy (PRESS) MRS was used to acquire data from the dentate gyrus and CA3 region of the hippocampus, assessing metabolite ratios to total creatine (tCr). In a subset of animals after the second imaging study, brains were analyzed histologically by Nissl staining.

Results: A hierarchical cluster analysis performed on the 3-day data from 21 kainate-treated animals (dentate gyrus voxel) segregated into two clusters, denoted by KM (more injured, n = 6) and KL (less injured, n = 15). Although there was no difference in kainate dosing or seizure count between them, the metabolic pattern of injury was different. The KM group displayed the largest significant changes in neuronal and glial parameters; the KL group displayed milder but significant changes. At 3 weeks, the KL group returned to normal compared to controls, whereas the KM group persisted with depressed N-acetyl aspartate (NAA)/tCr, glutamate/tCr, and increased inositol/tCr and glutamine/tCr. The classification was also consistent with subsequent histologic patterns at 3 weeks.

Significance: Although a short status period might be expected to generate a continuous distribution of metabolic injury, these data show that the short Hellier Dudek model appears to generate two levels of injury. The changes seen in segregated groups persisted into 3 weeks, and can be interpreted according to neuronal and glial biomarkers consistent with histology results.

Keywords: Glutamate; Kainate; Status epilepticus.

Publication types

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

MeSH terms

  • Animals
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / metabolism
  • Cluster Analysis
  • Creatine / metabolism
  • Disease Models, Animal
  • Electroencephalography
  • Excitatory Amino Acid Agonists / toxicity
  • Hippocampus / metabolism*
  • Kainic Acid / toxicity
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy
  • Male
  • Metabolic Diseases / diagnostic imaging
  • Metabolic Diseases / etiology*
  • Rats
  • Rats, Sprague-Dawley
  • Status Epilepticus / chemically induced
  • Status Epilepticus / complications*
  • Status Epilepticus / diagnostic imaging
  • Status Epilepticus / pathology
  • Time Factors
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Excitatory Amino Acid Agonists
  • Aspartic Acid
  • gamma-Aminobutyric Acid
  • N-acetylaspartate
  • Creatine
  • Kainic Acid