Literature DB >> 1909851

Epileptogenic effect of hypoxia in the immature rodent brain.

F E Jensen1, C D Applegate, D Holtzman, T R Belin, J L Burchfiel.   

Abstract

The response to cerebral hypoxia/ischemia may be different in the neonate compared to other age groups. An in vivo model was developed in the rat to determine whether there are age-dependent differences in the effects of hypoxia on electroencephalographic (EEG) activity. EEG recordings were obtained from Long Evans hooded rats deprived of oxygen at five ages: postnatal days 5 to 7, 10 to 12, 15 to 17, 25 to 27, and 50 to 60. Oxygen concentration was varied from 0, 2, 3, and 4% between animals. EEGs were recorded in all animals before, during, and at 1 hour after exposure to the hypoxic condition and at 1 to 7 days afterward in a subset of animals. All animals were deprived of oxygen until the onset of apnea and bradycardia to 20 to 40% of baseline heart rate values. Hypoxia resulted in isoelectric EEG significantly more frequently in the animals deprived of oxygen at postnatal days 25 to 27 and 50 to 60 than in the younger age groups. A highly significant effect was that the animals deprived at postnatal days 5 to 17 revealed a high incidence of epileptiform EEG activity during hypoxia. In contrast, the older animals exhibited only rare isolated EEG spikes before reaching an isoelectric EEG. The severity of hypoxia-induced epileptiform EEG changes was highest in the animals subjected to moderately hypoxic conditions (3% and 4% oxygen) at postnatal days 10 to 12. Furthermore, epileptiform changes persisted for hours to days following prolonged episodes of hypoxia in the younger animals. This study demonstrates a unique response of the immature brain to exhibit epileptiform activity during hypoxia.

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Year:  1991        PMID: 1909851     DOI: 10.1002/ana.410290610

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  52 in total

1.  Acute hypoxia differentially affects the NMDA receptor NR1, NR2A and NR2B subunit mRNA levels in the developing chick optic tectum: stage-dependent plasticity in the 2B-2A ratio.

Authors:  Marina Vacotto; Melina Rapacioli; Vladimir Flores; Sara Fiszer de Plazas
Journal:  Neurochem Res       Date:  2010-07-02       Impact factor: 3.996

2.  Downregulation of hippocampal GABA after hypoxia-induced seizures in neonatal rats.

Authors:  Yanmei Wang; Lixuan Zhan; Wei Zeng; Ke Li; Weiwen Sun; Zao C Xu; En Xu
Journal:  Neurochem Res       Date:  2011-08-11       Impact factor: 3.996

3.  Carbon dioxide and oxygen levels in disposable individually ventilated cages after removal from mechanical ventilation.

Authors:  Claude M Nagamine; C Tyler Long; Gabriel P McKeon; Stephen A Felt
Journal:  J Am Assoc Lab Anim Sci       Date:  2012-03       Impact factor: 1.232

4.  Hypoxia results in GABAergic channelopathy.

Authors:  Nicholas P Poolos
Journal:  Epilepsy Curr       Date:  2005 Nov-Dec       Impact factor: 7.500

5.  Developmental emergence of transient and persistent hippocampal events and oscillations and their association with infant seizure susceptibility.

Authors:  Ethan J Mohns; Karl A E Karlsson; Mark S Blumberg
Journal:  Eur J Neurosci       Date:  2007-10-31       Impact factor: 3.386

6.  Relationship between evolving epileptiform activity and delayed loss of mitochondrial activity after asphyxia measured by near-infrared spectroscopy in preterm fetal sheep.

Authors:  L Bennet; V Roelfsema; P Pathipati; J S Quaedackers; A J Gunn
Journal:  J Physiol       Date:  2006-02-16       Impact factor: 5.182

Review 7.  Living or dying in three quarter time: neonatal orchestration of hippocampal cell death pathways by androgens and excitatory GABA.

Authors:  C D Foradori; R J Handa
Journal:  Exp Neurol       Date:  2008-05-11       Impact factor: 5.330

Review 8.  Epileptogenesis in the immature brain: emerging mechanisms.

Authors:  Sanjay N Rakhade; Frances E Jensen
Journal:  Nat Rev Neurol       Date:  2009-07       Impact factor: 42.937

Review 9.  An animal model of hypoxia-induced perinatal seizures.

Authors:  F E Jensen
Journal:  Ital J Neurol Sci       Date:  1995 Feb-Mar

Review 10.  Neuropeptide-mediated excitability: a key triggering mechanism for seizure generation in the developing brain.

Authors:  T Z Baram; C G Hatalski
Journal:  Trends Neurosci       Date:  1998-11       Impact factor: 13.837

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