Literature DB >> 23973645

Maturation-dependent behavioral deficits and cell injury in developing animals during the subacute postictal period.

Lauren M Mlsna1, Sookyong Koh.   

Abstract

Prolonged early-life seizures are associated with disruptions of affective and cognitive function. Postictal disturbances, temporary functional deficits that persist for hours to days after seizures, have not yet been thoroughly characterized. Here, we used kainic acid (KA) to induce status epilepticus (SE) in immature rats at three developmental stages (postnatal day (P) 15, 21, or 30) and subsequently assessed spatial learning and memory in a Barnes maze, exploratory behavior in an open field, and the spatiotemporal distribution of cell injury during the first 7-10 days of the postictal period. At 1 day post-SE, P15-SE rats showed no deficit in the Barnes maze but were hyperexploratory in an open field compared with their littermate controls. In contrast, P21- and P30-SE rats exhibited markedly impaired performance in the Barnes maze and exhibited significantly reduced open field exploration suggestive of anxiety-like behavior. These behavioral changes were transient in P15 rats but more persistent in P21 and enduring in P30 rats after KA-SE. The time course of behavioral deficits in P21 and P30 rats was temporally correlated with the presence of neuronal injury in the lateral septal nuclei, amygdala, and ventral subiculum/CA1, regions involved in modulation of the hypothalamic-pituitary-adrenal stress response.
© 2013. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amygdala; Anxiety; BLA; Cell death; Epilepsy; HPA; ISEL; Immature brain; KA; LS; P; PBS; Postictal state; SE; Seizure; basolateral amygdala; hypothalamic–pituitary–adrenal; in situ end labeling; kainic acid; lateral septum; phosphate buffered saline; postnatal; status epilepticus; vSub/CA1; ventral subiculum/cornu ammonis 1

Mesh:

Substances:

Year:  2013        PMID: 23973645      PMCID: PMC3927371          DOI: 10.1016/j.yebeh.2013.07.018

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  91 in total

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