Sex- and age-dependent differences in sleep-wake characteristics of fisher-344 rats.

TitleSex- and age-dependent differences in sleep-wake characteristics of fisher-344 rats.
Publication TypeJournal Article
Year of Publication2020
AuthorsKostin A, Alam MAftab, Siegel JM, McGinty D, Alam MNoor
JournalNeuroscience
Volume427
Pagination29-42
Date Published2020 02 10
ISSN1873-7544
Abstract

Aging is a well-recognized risk factor for sleep disruption. The characteristics of sleep in aging include its disruption by frequent awakenings, a decline in both non-rapid eye movement (nonREM) and REM sleep amounts, and a weaker homeostatic response to sleep loss. Evidence also suggests that sleep in females is more sensitive to changes in the ovarian steroidal milieu. The Fischer-344 rats are commonly used experimental subjects in behavioral and physiological studies, including sleep and aging. Most sleep studies in Fischer-344 rats have used male subjects to avoid interactions between the estrus and sleep-waking cycles. The changes in the sleep-wake organization of female Fischer-344 rats, especially with advancing age, are not well-characterized. We determined sleep-waking features of cycling females across estrus stages. We also compared spontaneous and homeostatic sleep response profiles of young (3-4 months) and old (24-25 months) male and female Fischer-344 rats. The results suggest that: i) sleep-wake architectures across stages of estrus cycle in young females were largely comparable except for a significant suppression of REM sleep at proestrus night and an increase in REM sleep the following day; ii) despite hormonal differences, sleep-wake architecture in male and female rats of corresponding ages were comparable except for the suppression of REM sleep at proestrus night and higher nonREM delta power in recovery sleep; and iii) aging significantly affected sleep-wake amounts, sleep-wake stability, and homeostatic response to sleep loss in both male and female rats and that the adverse effects of aging were largely comparable in both sexes.

DOI10.1016/j.neuroscience.2019.11.046
Alternate JournalNeuroscience
PubMed ID31846749
PubMed Central IDPMC7194174
Grant ListR01 DA034748 / DA / NIDA NIH HHS / United States
R01 HL148574 / HL / NHLBI NIH HHS / United States