Literature DB >> 12193683

Impaired spatial learning and hyperactivity in developing rats exposed to intermittent hypoxia.

Barry W Row1, Leila Kheirandish, Jennifer J Neville, David Gozal.   

Abstract

Obstructive sleep apnea (OSA) is a frequent medical condition and is associated with cognitive impairments in adults and with hyperactivity and decreased school performance in children. In an adult rodent model, intermittent hypoxia (IH), such as occurs in OSA, is associated with neurodegenerative changes in the hippocampus and cortex and with spatial learning deficits. Because a unique developmental window of neural vulnerability to IH is present, we hypothesized that exposure to IH throughout the vulnerable ages would result in increased behavioral impairments in the juvenile rat. Rat pups were therefore exposed to either room air or IH beginning at postnatal (PN) d 10 until PN d 30. Learning and memory were assessed via a standard place-training version of the Morris water maze beginning at PN d 25. Locomotor activity was assessed on PN d 29 and 30. Pups exposed to IH displayed significant spatial learning impairments, and exposed male rats but not female rats displayed increased locomotor activity in the open field. Collectively, these findings indicate that exposure to IH at an age that corresponds to the peak incidence of OSA in children induces substantial learning impairment and gender-dependent behavioral hyperactivity in the juvenile rat. We postulate that this novel experimental model may allow for future exploration of mechanisms underlying the neurobehavioral deficits of children with OSA.

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Year:  2002        PMID: 12193683     DOI: 10.1203/00006450-200209000-00024

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  57 in total

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2.  Cholinesterase inhibitors ameliorate spatial learning deficits in rats following hypobaric hypoxia.

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Review 3.  Sex differences in neurodevelopmental abnormalities caused by early-life anaesthesia exposure: a narrative review.

Authors:  Omar H Cabrera; Thomas Gulvezan; Breanna Symmes; Nidia Quillinan; Vesna Jevtovic-Todorovic
Journal:  Br J Anaesth       Date:  2020-01-21       Impact factor: 9.166

4.  Neuronal death during combined intermittent hypoxia/hypercapnia is due to mitochondrial dysfunction.

Authors:  Robert M Douglas; Julie Ryu; Amjad Kanaan; Maria Del Carmen Rivero; Laura L Dugan; Gabriel G Haddad; Sameh S Ali
Journal:  Am J Physiol Cell Physiol       Date:  2010-03-31       Impact factor: 4.249

5.  SLEEP DISORDERED BREATHING AND METABOLIC EFFECTS: EVIDENCE FROM ANIMAL MODELS.

Authors:  Jonathan Jun; Vsevolod Y Polotsky
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6.  Exogenous growth hormone attenuates cognitive deficits induced by intermittent hypoxia in rats.

Authors:  R C Li; S Z Guo; M Raccurt; E Moudilou; G Morel; K R Brittian; D Gozal
Journal:  Neuroscience       Date:  2011-08-23       Impact factor: 3.590

Review 7.  Hypoxia-inducible factors and obstructive sleep apnea.

Authors:  Nanduri R Prabhakar; Ying-Jie Peng; Jayasri Nanduri
Journal:  J Clin Invest       Date:  2020-10-01       Impact factor: 14.808

Review 8.  Hypoxia-induced phrenic long-term facilitation: emergent properties.

Authors:  Michael J Devinney; Adrianne G Huxtable; Nicole L Nichols; Gordon S Mitchell
Journal:  Ann N Y Acad Sci       Date:  2013-03       Impact factor: 5.691

9.  Hippocampal spine-associated Rap-specific GTPase-activating protein induces enhancement of learning and memory in postnatally hypoxia-exposed mice.

Authors:  X-J Lu; X-Q Chen; J Weng; H-Y Zhang; D T Pak; J-H Luo; J-Z Du
Journal:  Neuroscience       Date:  2009-05-12       Impact factor: 3.590

10.  Network analysis of temporal effects of intermittent and sustained hypoxia on rat lungs.

Authors:  Wei Wu; Nilesh B Dave; Guoying Yu; Patrick J Strollo; Elizabeta Kovkarova-Naumovski; Stefan W Ryter; Stephen R Reeves; Ehab Dayyat; Yang Wang; Augustine M K Choi; David Gozal; Naftali Kaminski
Journal:  Physiol Genomics       Date:  2008-09-30       Impact factor: 3.107

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