Literature DB >> 20156487

Lateralized and sex-dependent behavioral and morphological effects of unilateral neonatal cerebral hypoxia-ischemia in the rat.

N S Arteni1, L O Pereira, A L Rodrigues, D Lavinsky, M E Achaval, C A Netto.   

Abstract

Neonatal cerebral hypoxia-ischemia (HI) is an important cause of neurological deficits. The Levine-Rice model of unilateral HI is a useful experimental tool, but the resulting brain damage is mainly restricted to one hemisphere. Since the rat presents morphological and biochemical asymmetries between brain hemispheres, behavioral outcome from this model is probably dependent on which hemisphere is damaged. We here investigated the effects of sex and lesioned hemisphere on the outcome of open field, plus maze, inhibitory avoidance and water maze tasks in adult rats previously submitted to neonatal unilateral HI. Females were more active than males in some of studied parameters and males presented better spatial learning. Hypoxia-ischemia caused spatial deficits independently of sex or damaged hemisphere. Right-HI increased locomotion only in males and caused working memory in females and on aversive learning in both males and females. Morphological analysis showed that right-HI animals presented greater reduction of ipsilateral striatum area, with females being more affected. Interestingly, males showed greater hippocampal volume. These results show that task performance and cerebral damage extension are lateralized and sex-dependent, and that the right hemisphere, irrespective of sex, is more vulnerable to neonatal cerebral hypoxia-ischemia.

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Year:  2010        PMID: 20156487     DOI: 10.1016/j.bbr.2010.02.015

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  23 in total

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2.  Chronic neurological deficits in mice after perinatal hypoxia and ischemia correlate with hemispheric tissue loss and white matter injury detected by MRI.

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3.  Administration of Huperzia quadrifariata Extract, a Cholinesterase Inhibitory Alkaloid Mixture, has Neuroprotective Effects in a Rat Model of Cerebral Hypoxia-Ischemia.

Authors:  F K Odorcyk; E F Sanches; F C Nicola; J Moraes; L F Pettenuzzo; J Kolling; C Siebert; A Longoni; E L Konrath; A Wyse; C A Netto
Journal:  Neurochem Res       Date:  2016-11-24       Impact factor: 3.996

4.  Sex differences in cell genesis, hippocampal volume and behavioral outcomes in a rat model of neonatal HI.

Authors:  Jaylyn Waddell; Marie Hanscom; N Shalon Edwards; Mary C McKenna; Margaret M McCarthy
Journal:  Exp Neurol       Date:  2015-09-12       Impact factor: 5.330

5.  Severe Hyperhomocysteinemia Decreases Creatine Kinase Activity and Causes Memory Impairment: Neuroprotective Role of Creatine.

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6.  Sexual dimorphism in BDNF signaling after neonatal hypoxia-ischemia and treatment with necrostatin-1.

Authors:  R Chavez-Valdez; L J Martin; S Razdan; E B Gauda; F J Northington
Journal:  Neuroscience       Date:  2013-12-17       Impact factor: 3.590

7.  Intracardiac Injection of Dental Pulp Stem Cells After Neonatal Hypoxia-Ischemia Prevents Cognitive Deficits in Rats.

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Journal:  Neurochem Res       Date:  2018-09-25       Impact factor: 3.996

8.  TrkB receptor agonist 7, 8 dihydroxyflavone triggers profound gender- dependent neuroprotection in mice after perinatal hypoxia and ischemia.

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Journal:  CNS Neurol Disord Drug Targets       Date:  2013-05-01       Impact factor: 4.388

Review 9.  Sex and steroid hormones in early brain injury.

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Journal:  Rev Endocr Metab Disord       Date:  2012-09       Impact factor: 6.514

10.  Early postnatal hypoxia induces behavioral deficits but not morphological damage in the hippocampus in adolescent rats.

Authors:  V Riljak; Z Laštůvka; J Mysliveček; V Borbélyová; J Otáhal
Journal:  Physiol Res       Date:  2019-12-19       Impact factor: 1.881

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