Subscribe to RSS

DOI: 10.1590/0004-282X20160070
Impaired executive functions in experimental model of temporal lobe epilepsy
Prejuízo das funções executivas no modelo experimental de epilepsia do lobo temporal Supported: This work was sponsored by grants from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-302528/2011-3) and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP-2011/50680-2). Fabiane Ochai Ramos was fellow from CNPq.
ABSTRACT
Objective The present study aimed to investigate cognitive and behavioural changes consistent with attention deficit hyperactivity disorder (ADHD -like behavior in male Wistar rats with temporal lobe epilepsy (TLE).
Method Male Wistar rats at 25 day of age were submitted to animal model of TLE by pilocarpine injection (350 mg/kg, ip) and a control group received saline 0.9%. The animals were continuously video monitored up to the end of experiments. The behavioural tests (open field, elevated plus maze and operant conditioning box) started from 60 days postnatal.
Results Animals with TLE exhibited elevated locomotor activity, reduced level of anxiety-related behavior, impulsivity and impaired visuospatial working memory.
Conclusion Taken as a whole, we concluded that animals with TLE exhibited some cognitive and behavioural changes consistent with ADHD-like behavior.
RESUMO
Objetivo O presente estudo teve como objetivo investigar as alterações cognitivas e comportamentais consistentes com o comportament de transtorno de deficit de atenção e hiperatividade (TDAH) -like em ratos Wistar machos com epilepsia do lobo temporal (ELT).
Método Ratos Wistar machos com 25 dias de vida foram submetidos a modelo animal de ELT pela injeção de pilocarpina (350 mg / kg, ip) e grupo controle recebeu salina 0,9%. Os animais foram monitorados continuamente por vídeo até ao final dos experimentos. Os testes comportamentais (campo aberto, labirinto em cruz elevado e caixa de condicionamento operante) começaram a partir de 60 dias pós-natal.
Resultados Os animais com ELT exibiram aumento da atividade locomotora, redução do comportamento relacionado com a ansiedade, impulsividade e prejuízo da memória de trabalho visuospatial.
Conclusão Em conjunto, concluímos que os animais com ELT apresentaram algumas alterações cognitivas e comportamentais consistentes com o comportamento TDAH-like.
Support:
Supported: This work was sponsored by grants from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-302528/2011-3) and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP-2011/50680-2). Fabiane Ochai Ramos was fellow from CNPq.
Publication History
Received: 11 November 2015
Accepted: 15 March 2016
Article published online:
06 September 2023
© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
-
References
- 1 Sander JW. The epidemiology of epilepsy revisited. Curr Opin Neurol. 2003;16(2):165-70. doi:10.1097/00019052-200304000-00008
- 2 Boer HM, Mula M, Sander JW. The global burden and stigma of epilepsy. Epilepsy Behavior. 2008;12(4):540-6. doi:10.1016/j.yebeh.2007.12.019
- 3 Thurman DJ, Beghi E, Begley CE, Berg AT, Buchhalter JR, Ding D. Standards for epidemiologic studies and surveillance of epilepsy. Epilepsia. 2011;52(suppl 7):2-26. doi:10.1111/j.1528-1167.2011.03121.x
- 4 Laxer KD, Trinka E, Hirsch LJ, Cendes F, Langfitt J, Delanty N et al. The consequences of refractory epilepsy and its treatment. Epilepsy Behav. 2014;37:59-70. doi:10.1016/j.yebeh.2014.05.031
- 5 Duncan JS, Sander JW, Sisodiya SM, Walker MC. Adult epilepsy. Lancet. 2006;367(9516):14. doi:10.1016/S0140-6736(06)68477-8
- 6 Kwan P, Sander JW. The natural history of epilepsy: an epidemiological view. J Neurol Neurosurg Psychiatry. 2004;75(10):1376-81. doi:10.1136/jnnp.2004.045690
- 7 Sander JW. Some aspects of prognosis in the epilepsies: a review. Epilepsia. 1993;34(6):1007-16. doi:10.1111/j.1528-1157.1993.tb02126.x
- 8 Zamarian L, Trinka E, Bonatti E, Kuchukhidze G, Bodner T, Benke T et al. Executive functions in chronic mesial temporal lobe epilepsy. Epilepsy Res Treat. 2011;2011:ID596174. doi:10.1155/2011/596174
- 9 Stretton J, Winston GP, Sidhu M, Bonelli S, Centeno M, Vollmar C et al. Disrupted segregation of working memory networks in temporal lobe epilepsy. Neuroimage Clin. 2013;2:273-81. doi:10.1016/j.nicl.2013.01.009
- 10 Cohen R, Senecky Y, Shuper A, Inbar D, Chodick G, Shalev V et al. Prevalence of epilepsy and attention-deficit hyperactivity (ADHD) disorder: a population-based study. J Child Neurol. 2013;28(1):120-3. doi:10.1177/0883073812440327
- 11 Dunn DW, Austin JK, Harezlak J, Ambrosius WT. ADHD and epilepsy in childhood. Develop Med Child Neurol. 2003;45(1):50-4. doi:10.1111/j.1469-8749.2003.tb00859.x
- 12 Loutfi KS, Carvalho AM. Possíveis interfaces entre TDAH e epilepsia. J Bras Psiquiatr. 2010;59(2):146-55. doi:10.1590/S0047-20852010000200011
- 13 Turski WA, Cavalheiro EA, Schwarz M, Czuczwar SJ, Kleinrok Z, Turski L. Limbic seizures produced by pilocarpine in rats: behavioural, electroencephalographic and neuropathological study. Behav Brain Res. 1983;9(3):315-35. doi:10.1016/0166-4328(83)90136-5
- 14 Levant B, Zarcone TJ, Davis PF, Ozias MK, Fowler SC. Differences in methylphenidate dose response between periadolescent and adult rats in the familiar arena-novel alcove task. J Pharmacol Exp Ther. 2011;337(1):83-91. doi:10.1124/jpet.110.174425
- 15 Kubová H, Haugvicová R, Suchomelová L, Mares P. Does status epilepticus influence the motor development of immature rats? Epilepsia. 2000;41(Suppl 6):S64-9. doi:10.1111/j.1528-1157.2000.tb01559.x
- 16 Detour J, Schroeder H, Desor D, Nehlig A. 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;46(4):499-508. doi:10.1111/j.0013-9580.2005.38704.x
- 17 Inostroza M, Cid E, Menendez de la Prida L, Sandi C. Different emotional disturbances in two experimental models of temporal lobe epilepsy in rats. PLoS One. 2012;7(6):e38959. doi:10.1371/journal.pone.0038959
- 18 Pineda E, Jentsch JD, Shin D, Griesbach G, Sankar R, Mazarati A. Behavioral impairments in rats with chronic epilepsy suggest comorbidity between epilepsy and attention deficit/hyperactivity disorder. Epilepsy Behav. 2014;31:267-75. doi:10.1016/j.yebeh.2013.10.004
- 19 Faure JB, Marques-Carneiro JE, Akimana G, Cosquer B, Ferrandon A, Herbeaux K et al. Attention and executive functions in a rat model of chronic epilepsy. Epilepsia. 2014;55(5):644-53. doi:10.1111/epi.12549
- 20 Arida RM, Scorza FA, Peres CA, Cavalheiro EA. The course of untreated seizures in the pilocarpine model of epilepsy. Epilepsy Res. 1999;34(2-3):99-107. doi:10.1016/S0920-1211(98)00092-8
- 21 Bajorat R, Wilde M, Sellmann T, Kirschstein T, Köhling R. Seizure frequency in pilocarpine-treated rats is independent of circadian rhythm. Epilepsia. 2011;52(9):e118-22. doi:10.1111/j.1528-1167.2011.03200.x
- 22 Liu RS, Lemieux L, Bell GS, Hammers A, Sisodiya SM, Bartlett PA et al. Progressive neocortical damage in epilepsy. Ann Neurol. 2003;53(3):312-24. doi:10.1002/ana.10463
- 23 Cascino GD. Progressive damage in epilepsy. Epilepsy Curr. 2003;3(6):214-5. doi:10.1046/j.1535-7597.2003.03615.x
- 24 Fuerst D, Shah J, Shah A, Watson C. Hippocampal sclerosis is a progressive disorder: a longitudinal volumetric MRI study. Ann Neurol. 2003;53(3):413-6. doi:10.1002/ana.10509
- 25 Briellmann RS, Berkovic SF, Syngeniotis A, King MA, Jackson GD. Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy. Ann Neurol. 2002;51(5):641-4. doi:10.1002/ana.10171
- 26 Liu RS, Lemieux L, Bell GS, Sisodiya SM, Bartlett PA, Shorvon SD et al. Cerebral damage in epilepsy: a population-based longitudinal quantitative MRI study. Epilepsia. 2005;46(9):1482-94. doi:10.1111/j.1528-1167.2005.51603.x
- 27 Pacagnella D, Lopes TM, Morita ME, Yasuda CL, Cappabianco FA, Bergo F et al. Memory impairment is not necessarily related to seizure frequency in mesial temporal lobe epilepsy with hippocampal sclerosis. Epilepsia. 2014;55(8):1197-204. doi:10.1111/epi.12691
- 28 Abrahams S, Morris RG, Polkey CE, Jarosz JM, Cox TC, Graves M et al. Hippocampal involvement in spatial and working memory: a structural MRI analysis of patients with unilateral mesial temporal lobe sclerosis. Brain Cogn. 1999;41(1):39-65. doi:10.1006/brcg.1999.1095
- 29 Krauss GL, Summerfield M, Brandt J, Breiter S, Ruchkin D. Mesial temporal spikes interfere with working memory. Neurology. 1997;49(4):975-80. doi:10.1212/WNL.49.4.975
- 30 Owen AM, Morris RG, Sahakian BJ, Polkey CE, Robbins TW. Double dissociations of memory and executive functions in working memory tasks following frontal lobe excisions, temporal lobe excisions or amygdalo-hippocampectomy in man. Brain. 1996;119(5):1597-615. doi:10.1093/brain/119.5.1597
- 31 Doucet G, Osipowicz K, Sharan A, Sperling MR, Tracy JI. Hippocampal functional connectivity patterns during spatial working memory differ in right versus left temporal lobe epilepsy. Brain Connect. 2013;3(4):398-406. doi:10.1089/brain.2013.0158