Literature DB >> 16997287

Adult neurological function following neonatal hypoxia-ischemia in a mouse model of the term neonate: water maze performance is dependent on separable cognitive and motor components.

John J McAuliffe1, Lili Miles, Charles V Vorhees.   

Abstract

BACKGROUND AND
PURPOSE: Hypoxic-ischemic injury in term neonates remains a significant cause of long-term neurological morbidity. The post-natal day 10 (P10) mouse is accepted as a model for the term human. This study was designed to assess the relationships between the duration of hypoxia-ischemia (HI) on P10 and the structural and functional neurological deficits that appear in the adult mouse as a consequence.
METHODS: Post-natal day 10 129T2xC57Bl/6 F1 hybrid mice were subjected to 0, 45, 60 or 75 min of hypoxia-ischemia using the Rice-Vannucci model. Beginning on P50 these mice were tested over the next 8 weeks using zero maze, locomotor activity, novel object recognition, cued, hidden and reduced Morris water mazes, delayed probe trials and response to apomorphine injection. Brain weights and histology were obtained at the end of testing.
RESULTS: The degree of structural and behavioral abnormalities in adult mice correlated with the duration of hypoxia-ischemia on P10. Useful behavioral tests for separating adult mice according to duration of hypoxia-ischemia on P10 include locomotor activity, the Morris water mazes and response to apomorphine. We found cued "learning" persisted, although latencies increased, with increasing HI time while spatial learning decayed as a function of HI time. Severe HI injury involving the ventral hippocampus resulted in excessive locomotor activity.
CONCLUSIONS: After correcting for motor deficits, there is evidence for persistence of "cued" learning but not spatial learning with increasing hypoxia-ischemia time on P10 in this model system.

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Year:  2006        PMID: 16997287     DOI: 10.1016/j.brainres.2006.08.030

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  8 in total

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2.  Suppression of microglia activation after hypoxia-ischemia results in age-dependent improvements in neurologic injury.

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4.  Inhibition of Na+/H+ exchanger isoform 1 is neuroprotective in neonatal hypoxic ischemic brain injury.

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Review 5.  Brain development in rodents and humans: Identifying benchmarks of maturation and vulnerability to injury across species.

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6.  Altered behavioral phenotypes in soluble epoxide hydrolase knockout mice: effects of traumatic brain injury.

Authors:  Kenneth I Strauss; Artiom Gruzdev; Darryl C Zeldin
Journal:  Prostaglandins Other Lipid Mediat       Date:  2012-08-16       Impact factor: 3.072

7.  Short and long-term analysis and comparison of neurodegeneration and inflammatory cell response in the ipsilateral and contralateral hemisphere of the neonatal mouse brain after hypoxia/ischemia.

Authors:  Kalpana Shrivastava; Mariela Chertoff; Gemma Llovera; Mireia Recasens; Laia Acarin
Journal:  Neurol Res Int       Date:  2012-06-03

8.  Nesting Environment Provides Sex-Specific Neuroprotection in a Rat Model of Neonatal Hypoxic-Ischemic Injury.

Authors:  Briana Mason; L G Rollins; Evans Asumadu; Christina Cange; Najah Walton; S Tiffany Donaldson
Journal:  Front Behav Neurosci       Date:  2018-10-02       Impact factor: 3.558

  8 in total

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