Prenatal Exposure to Carbamazepine Reduces Hippocampal and Cortical Neuronal Cell Population in New-Born and Young Mice without Detectable Effects on Learning And Memory

被引:14
作者
Aberg, Elin [1 ,2 ]
Holst, Sarah [3 ]
Neagu, Alexandru [1 ,2 ]
Ogren, Sven Ove [3 ]
Lavebratt, Catharina [1 ,2 ]
机构
[1] Karolinska Inst, Dept Mol Med & Surg, Neurogenet Unit, Stockholm, Sweden
[2] Karolinska Univ Hosp, Ctr Mol Med, Stockholm, Sweden
[3] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
基金
英国医学研究理事会;
关键词
UNBIASED STEREOLOGICAL ESTIMATION; MAJOR CONGENITAL-MALFORMATIONS; DRUGS IN-UTERO; ANTIEPILEPTIC DRUGS; CHILDREN BORN; ANTICONVULSANT DRUGS; DEVELOPING BRAIN; WATER-MAZE; EPILEPSY; PREGNANCY;
D O I
10.1371/journal.pone.0080497
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pregnant women with epilepsy have to balance maternal and fetal risks associated with uncontrolled seizures against the potential teratogenic effects from antiepileptic drugs (AEDs). Carbamazepine (CBZ) is among the four most commonly used AEDs for treatment of pregnant epileptic women. We previously reported that new-born children had a decreased head circumference after in utero CBZ exposure. This study investigates how prenatal exposure of CBZ influences the number of neurons in new-born and young mouse hippocampus, amygdala and cortex cerebri. Clinical studies describe inconclusive results on if prenatal CBZ treatment influences cognition. Here we investigate this issue in mice using two well characterized cognitive tasks, the passive avoidance test and the Morris water maze test. Prenatal exposure of CBZ reduced the number of neurons (NeuN-immunoreactive cells) in the new-born mouse hippocampus with 50% compared to non-exposed mice. A reduction of neurons (20%) in hippocampus was still observed when the animals were 5 weeks old. These mice also displayed a 25% reduction of neurons in cortex cerebri. Prenatal CBZ treatment did not significantly impair learning and memory measured in the passive avoidance test and in the Morris water maze. However, these mice displayed a higher degree of thigmotaxic behaviour than the control mice. The body weight of prenatally CBZ exposed five-week old mice were lower compared to control mice not exposed to CBZ (p = 0.001). In conclusion, prenatal exposure to CBZ reduces the number of neurons dramatically in areas important for cognition such as hippocampus and cortex, without severe impairments on learning and memory. These results are in line with some clinical studies, reporting that CBZ has minor negative effects on cognition. The challenge for future studies are to segment out what possible effects a reduction of neurons could have on different types of cognition, like intellectual ability and social interaction.
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页数:8
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共 65 条
[1]   The longer term outcome of children born to mothers with epilepsy [J].
Adab, N ;
Kini, U ;
Vinten, J ;
Ayres, J ;
Baker, G ;
Clayton-Smith, J ;
Coyle, H ;
Fryer, A ;
Gorry, J ;
Gregg, J ;
Mawer, G ;
Nicolaides, P ;
Pickering, L ;
Tunnicliffe, L ;
Chadwick, DW .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2004, 75 (11) :1575-1583
[2]   Additional educational needs in children born to mothers with epilepsy [J].
Adab, N ;
Jacoby, A ;
Smith, D ;
Chadwick, D .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 70 (01) :15-21
[3]  
ADAB N, 2004, COCHRANE DB SYST REV, DOI DOI 10.1002/14651858.CD004848
[4]   Population-based study of antiepileptic drug exposure in utero-Influence on head circumference in newborns [J].
Almgren, Malin ;
Kallen, Bengt ;
Lavebratt, Catharina .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2009, 18 (10) :672-675
[5]   Differential involvement of the dorsal hippocampus in passive avoidance in C57BL/6J and DBA/2J mice [J].
Baarendse, Petra J. J. ;
Van Grootheest, Gerard ;
Jansen, Rene F. ;
Pieneman, Anton W. ;
Ogren, Sven Ove ;
Verhage, Matthijs ;
Stiedl, Oliver .
HIPPOCAMPUS, 2008, 18 (01) :11-19
[6]   Long-Term Developmental Outcome of Children of Women with Epilepsy, Unexposed or Exposed Prenatally to Antiepileptic Drugs A Meta-Analysis of Cohort Studies [J].
Banach, Ryan ;
Boskovic, Radinka ;
Einarson, Thomas ;
Koren, Gideon .
DRUG SAFETY, 2010, 33 (01) :73-79
[7]   HIPPOCAMPAL DEVELOPMENT IN RAT - CYTOGENESIS AND MORPHOGENESIS EXAMINED WITH AUTORADIOGRAPHY AND LOW-LEVEL X-IRRADIATION [J].
BAYER, SA ;
ALTMAN, J .
JOURNAL OF COMPARATIVE NEUROLOGY, 1974, 158 (01) :55-79
[8]   Antiepileptic drugs and apoptotic neurodegeneration in the developing brain [J].
Bittigau, P ;
Sifringer, M ;
Genz, K ;
Reith, E ;
Pospischil, D ;
Govindarajalu, S ;
Dzietko, M ;
Pesditschek, S ;
Mai, I ;
Dikranian, K ;
Olney, JW ;
Ikonomidou, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) :15089-15094
[9]   Cognitive abilities and behaviour of children exposed to antiepileptic drugs in utero [J].
Bromley, Rebecca L. ;
Baker, Gus A. ;
Meador, Kimford J. .
CURRENT OPINION IN NEUROLOGY, 2009, 22 (02) :162-166
[10]   Apoptotic features of selective neuronal death in ischemia, epilepsy and gp120 toxicity [J].
CharriautMarlangue, C ;
AggounZouaoui, D ;
Represa, A ;
BenAri, Y .
TRENDS IN NEUROSCIENCES, 1996, 19 (03) :109-114