Literature DB >> 17716797

Distinct behavioral and neurochemical alterations induced by intermittent hypoxia or paradoxical sleep deprivation in rats.

Juliana C Perry1, Vânia D'Almeida, Isabela B Antunes, Sergio Tufik.   

Abstract

The current study investigated the effects of paradoxical sleep deprivation and intermittent hypoxia by examining whether a combination of the two would induce anxiety-like alterations in behavior. The neurochemical effects of these manipulations were investigated by measuring cortical, striatal and hippocampal monoamine concentrations. Wistar Hannover rats were submitted to subchronic (3 days) intermittent hypoxia exposure (alternating cycles of 2 min room air-2 min 10% O2 from 0700-1900 h) and paradoxical sleep deprivation using the single platform method. Rats were randomly assigned to four different protocols: 1) control, 2) intermittent hypoxia during the light period (12 h/day), 3) paradoxical sleep deprivation (24 h/day), and 4) intermittent hypoxia combined with paradoxical sleep deprivation. Rats subjected to intermittent hypoxia showed no modification in the behavioral or neurochemical parameters assessed. Although paradoxical sleep deprivation did not produce alterations in anxiety-like behavior, the rats did increase exploratory activity in the elevated plus-maze. Moreover, a significant increase in striatal epinephrine and hippocampal homovanilic acid (HVA) concentrations was found in the paradoxical sleep deprivation groups, but not in the intermittent hypoxia/paradoxical sleep deprivation group. Of note, both paradoxical sleep deprivation and intermittent hypoxia/paradoxical sleep deprivation groups showed an increase in plasma corticosterone concentration. These results suggest that paradoxical sleep deprivation induces behavioral alterations, and these abnormalities may reflect altered neurotransmission in the brain. When paradoxical sleep deprivation was combined with intermittent oxygen depletion, the behavioral and biochemical parameters were comparable to those of control rats.

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Year:  2007        PMID: 17716797     DOI: 10.1016/j.pnpbp.2007.07.017

Source DB:  PubMed          Journal:  Prog Neuropsychopharmacol Biol Psychiatry        ISSN: 0278-5846            Impact factor:   5.067


  7 in total

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2.  Dim light at night interacts with intermittent hypoxia to alter cognitive and affective responses.

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Journal:  PLoS One       Date:  2019-07-03       Impact factor: 3.240

5.  The Prevalence of Anxiety and Depression Symptoms in Obstructive Sleep Apnea.

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6.  NADPH oxidase elevations in pyramidal neurons drive psychosocial stress-induced neuropathology.

Authors:  S Schiavone; V Jaquet; S Sorce; M Dubois-Dauphin; M Hultqvist; L Bäckdahl; R Holmdahl; M Colaianna; V Cuomo; L Trabace; K-H Krause
Journal:  Transl Psychiatry       Date:  2012-05-08       Impact factor: 6.222

7.  Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State.

Authors:  Željko Grubač; Nikola Šutulović; Sonja Šuvakov; Djurdja Jerotić; Nela Puškaš; Djuro Macut; Aleksandra Rašić-Marković; Tatjana Simić; Olivera Stanojlović; Dragan Hrnčić
Journal:  Oxid Med Cell Longev       Date:  2021-08-21       Impact factor: 6.543

  7 in total

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