Volume 40, Issue 9 pp. 1177-1183

Cognitive Functions After Pilocarpine-Induced Status Epilepticus: Changes During Silent Period Precede Appearance of Spontaneous Recurrent Seizures

Jakub Hort

Jakub Hort

Department of Physiology, Charles University, Prague, Czech Republic

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Gustav Broźek

Corresponding Author

Gustav Broźek

Institute of Physiology, Academy of Sciences of the Czech Republic

Department of Physiology, Charles University, Prague, Czech Republic

Address correspondence and reprint requests to Dr. G. Broźek at Institute of Physiology, Academy of Sciences of the Czech Republic, Videnská 1083, CZ-142 20 Prague 4, Czech Republic. E-mail: [email protected]Search for more papers by this author
Pavel Mareš

Pavel Mareš

Institute of Physiology, Academy of Sciences of the Czech Republic

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Miloš Langmeier

Miloš Langmeier

Department of Physiology of the 1st Medical School, Charles University, Prague, Czech Republic

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Vladimír Komárek

Vladimír Komárek

Department of Child Neurology of the 2nd Medical School, Charles University, Prague, Czech Republic

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First published: 02 August 2005
Citations: 69

Abstract

Summary: Purpose: To study the possible relation between spontaneous recurrent seizures (SRS) and the derangement of cognitive memory.

Methods: Status epilepticus (SE) was induced in adult Long-Evans rats by pilocarpine (320 mg/kg, i.p.) and interrupted after 2 h by clonazepam (CZPs mg/kg, i.p.). In addition to the animals that were given pilocarpine and CZP (group P), two groups received ketamine (100 mg/kg, i.p.): the first group 15 minutes after SE onset (group K15), and the second immediately after the CZP (group K120). Control groups were formed from animals not treated with pilocarpine as well as animals that received pilocarpine but did not develop motor seizures. Spatial cognitive memory was tested in the Morris water maze.

Results: Testing was impossible for more than 6 days after SE in group P. Ketamine shortened this period for the two groups that received it. During the silent period, deteriorated cognitive memory progressively improved, but the performance of group P started to worsen before the appearance of SRS. Group K120 only expressed a tendency toward declining performance, whereas group K15 never developed SRS, and the behavior of these animals did not differ from that of the controls after the postseizure period was over. Histologically, massive hippocampal cell loss was seen in group P. Ketamine protected hippocampal cells in a time-dependent manner; group K15 did not exhibit any obvious necrosis in the hippocampus.

Conclusions: There is no close relation between cognitive functions and the appearance of SRS, because ketamine, administered 120 min after the beginning of SE, prevented the derangment of cognitive functions but not the appearance of SRSs.

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