| Literature DB >> 26657022 |
Grace Violeta Espinoza Pardo1, Jéferson Ferraz Goularte2, Ana Lúcia Hoefel3, Alexandre Luz de Castro4, Luiz Carlos Kucharski5, Alex Sander da Rosa Araujo6, Aldo Bolten Lucion7.
Abstract
The present study aimed to analyze the effects of sleep restriction (SR) during pregnancy in rats. The following three groups were studied: home cage (HC pregnant females remained in their home cage), Sham (females were placed in tanks similar to the SR group but with sawdust) and SR (females were submitted to the multiple platform method for 20 h per day from gestational days (GD) 14 to 20). Plasma corticosterone after 6 days of SR was not different among the groups. However, the relative adrenal weight was higher in the SR group compared with the HC group, which suggests possible stress impact. SR during pregnancy reduces the body weight of the female but no changes in liver glycogen, cholesterol and triglycerides, and muscle glycogen were detected. On GD 20, the fetuses of the females submitted to SR exhibited increased brain derived neurotrophic factor (BDNF) in the hippocampus, which indicates that sleep restriction of mothers during the final week of gestation may affect neuronal growth factors in a fetal brain structure, in which active neurogenesis occurs during the deprivation period. However, no changes in the total reactive oxygen species (ROS) in the cortex, hippocampus, or cerebellum of the fetuses were detected. SR females showed no major change in the maternal behavior, and the pups' preference for the mother's odor on postpartum day (PPD) 7 was not altered. On GD 20, the SR females exhibited increased plasma prolactin (PRL) and oxytocin (OT) compared with the HC and Sham groups. The negative outcomes of sleep restriction during delivery could be related, in part, to this hormonal imbalance. Sleep restriction during pregnancy induces different changes compared with the changes described in males and affects both the mother and offspring.Entities:
Keywords: BDNF; Corticosterone; Maternal behavior; Oxytocin; Prolactin; ROS
Mesh:
Substances:
Year: 2015 PMID: 26657022 DOI: 10.1016/j.physbeh.2015.11.037
Source DB: PubMed Journal: Physiol Behav ISSN: 0031-9384