A 5-month period of epilepsy impairs spatial memory, decreases anxiety, but spares object recognition in the lithium-pilocarpine model in adult rats

Epilepsia. 2005 Apr;46(4):499-508. doi: 10.1111/j.0013-9580.2005.38704.x.

Abstract

Purpose: In temporal lobe epilepsy (TLE), interictal behavioral disorders affect patients' quality of life. Therefore we studied long-term behavioral impairments in the lithium-pilocarpine (li-pilo) model of TLE.

Methods: Eleven li-pilo adult rats exhibiting spontaneous recurrent seizures (SRSs) during 5 months were compared with 11 li-saline rats. Spatial working memory was tested in a radial arm maze (RAM), anxiety in an elevated plus-maze (EPM), and nonspatial working memory in an object-recognition paradigm. Neuronal loss was assessed on thionine brain sections after behavioral testing.

Results: In the RAM, the time to complete each session and the number of errors per session decreased over a 5-day period in li-saline rats but remained constant and significantly higher in li-pilo rats. In the EPM, the number of entries in and time spent on open arms were significantly higher in li-pilo than li-saline rats. In the object-recognition task, the two groups exhibited a comparable novelty preference for the new object. Neuronal loss reached 47-90% in hilus, CA1, amygdala, and piriform and entorhinal cortex.

Conclusions: In li-pilo rats having experienced SRS for 5 months, performance in the object-recognition task is spared, which suggests that object discrimination remains relatively intact despite extensive damage. Neuronal loss in regions mediating memory and anxiety, such as hippocampus, entorhinal cortex, and amygdala, may relate to impaired spatial orientation and decreased anxiety.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anxiety / etiology
  • Anxiety / pathology
  • Anxiety / psychology*
  • Behavior, Animal* / drug effects
  • Behavior, Animal* / physiology
  • Cell Count
  • Disease Models, Animal*
  • Entorhinal Cortex / drug effects
  • Entorhinal Cortex / pathology
  • Entorhinal Cortex / physiology
  • Epilepsy, Temporal Lobe / chemically induced*
  • Epilepsy, Temporal Lobe / pathology
  • Epilepsy, Temporal Lobe / psychology*
  • Exploratory Behavior / drug effects
  • Exploratory Behavior / physiology
  • Hippocampus / drug effects
  • Hippocampus / pathology
  • Hippocampus / physiology
  • Lithium / administration & dosage
  • Lithium / pharmacology
  • Maze Learning / drug effects
  • Maze Learning / physiology
  • Memory Disorders / pathology
  • Memory Disorders / psychology*
  • Neurons / drug effects
  • Neurons / pathology
  • Neurons / physiology
  • Parahippocampal Gyrus / drug effects
  • Parahippocampal Gyrus / pathology
  • Parahippocampal Gyrus / physiology
  • Pilocarpine / administration & dosage
  • Pilocarpine / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Seizures / chemically induced
  • Seizures / pathology
  • Seizures / psychology
  • Spatial Behavior* / drug effects*
  • Spatial Behavior* / physiology

Substances

  • Pilocarpine
  • Lithium