- Open Access
Maternal sleep deprivation at different stages of pregnancy impairs the emotional and cognitive functions, and suppresses hippocampal long-term potentiation in the offspring rats
- Yan Peng†1, 2,
- Wei Wang†1, 2,
- Tao Tan1, 2,
- Wenting He1, 2,
- Zhifang Dong1, 2,
- Yu Tian Wang1, 2, 3 and
- Huili Han1, 2Email author
© Peng et al. 2016
- Received: 17 December 2015
- Accepted: 3 February 2016
- Published: 15 February 2016
Sleep deprivation during pregnancy is a serious public health problem as it can affect the health of pregnant women and newborns. However, it is not well studied whether sleep deprivation at different stages of pregnancy has similar effects on emotional and cognitive functions of the offspring, and if so, the potential cellular mechanisms also remain poorly understood.
In the present study, the pregnant rats were subjected to sleep deprivation for 6 h per day by gentle handling during the first (gestational days 1–7), second (gestational days 8–14) and third trimester (gestational days 15–21) of pregnancy, respectively. The emotional and cognitive functions as well as hippocampal long-term potentiation (LTP) were tested in the offspring rats (postnatal days 42-56).
The offspring displayed impaired hippocampal-dependent spatial learning and memory, and increased depressive- and anxiety-like behaviors. Quantification of BrdU-positive cells revealed that adult hippocampal neurogenesis was significantly reduced compared to control. Electrophysiological recording showed that maternal sleep deprivation impaired hippocampal CA1 LTP and reduced basal synaptic transmission, as reflected by a decrease in the frequency and amplitude of miniature excitatory postsynaptic current in the hippocampal CA1 pyramidal neurons.
Taken together, these results suggest that maternal sleep deprivation at different stages of pregnancy disrupts the emotional and cognitive functions of the offspring that might be attributable to the suppression of hippocampal LTP and basal synaptic transmission.
- Maternal sleep deprivation
- Spatial learning and memory
- Long-term potentiation
Sleep is a basic necessity for survival, since long-term sleep deprivation leads to severe physical and cognitive impairment, even death . However, about 50 % people throughout the world encounter one or more sleep disorders including insomnia, narcolepsy, somnambulism and the circadian rhythm sleep disorders . Sleep disorders are especially prevalent in pregnancy due to a series of obvious reasons including pregnancy-associated hormonal, physical and behavioral changes [3, 4]. Accumulating evidence shows that sleep deprivation during pregnancy not only increases the risk of maternal psychiatric disorders , but also leads to several harmful consequences to the offspring. For example, maternal sleep deprivation impairs adult neurogenesis and hippocampus-dependent spatial learning and memory in the offspring rats [6, 7]. Furthermore, sleep deprivation during pregnancy leads to the lower sexual behavior of the male offspring  and increased risk-taking behavior in offspring [9, 10].
Although maternal sleep deprivation has been shown to cause behavioral alterations in offspring [6–11], there are few reports on the effects of sleep deprivation at different stages of pregnancy on emotional and cognitive functions of the offspring. And potential mechanisms underlying such effects also remain poorly understood. The hippocampal dentate gyrus plays a critical role in learning and memory throughout life, in part due to continuing neurogenesis occurrence in this area. There is a growing body of evidence showing that sleep deprivation reduces dentate gyrus neurogenesis, which may contribute to the deficit of hippocampal-dependent cognitive function [12–14]. However, the effects of sleep deprivation at different stages of pregnancy on adult hippocampal neurogenesis have not been extensively studied, although a recent report has showed that maternal sleep deprivation inhibits hippocampal neurogenesis in the young offspring rats . In addition, several forms of synaptic plasticity in the CA1 area of the hippocampus, such as long-term potentiation (LTP) and long-term depression (LTD), have been proposed as the cellular mechanisms of information processing and memory formation [15–18]. Recent studies have demonstrated that sleep deprivation impairs hippocampal LTP [19, 20], which may be attributed to the disruption of cyclic adenosine monophosphate signaling . However, there is no report about the influence of maternal sleep deprivation on hippocampal CA1 LTP in offspring.
Thus, the present study aimed to determine whether sleep deprivation at different stages of pregnancy affects emotional and cognitive functions of the offspring, and if so, whether this influence is related to adult hippocampal neurogenesis and hippocampal CA1 LTP in the offspring.
Female and male Sprague–Dawley rats were obtained from Chongqing Medical University Animal Care Centre, and they mated in the laboratory colony of Children’s Hospital of Chongqing Medical University. The offspring of these rats were used in the present study. Pregnant females were housed individually in plastic cages in the temperature-controlled (21 °C) colony room on a 12/12 h light/dark cycle (8:00 a.m.–8:00 p.m.), and were free to food and water. The pregnant rats were divided into 4 groups: normal rearing (control), sleep deprivation at early pregnancy stage (ESD, gestational days 1–7), sleep deprivation at middle pregnancy stage (MSD, gestational days 8–14) and sleep deprivation at late pregnancy stage (LSD, gestational days 15–21). Within 24 h of birth, all litters were culled to 10 pups with a goal of balancing the number of males and females equally. Young adult rats from postnatal day (PND) 42–56 were used for behavioral and electrophysiological experiments. All experimental protocols were approved by Chongqing Medical University Animal Care Committee.
The sleep deprivation was performed by gentle handling for 6 h per day (12:00–18:00) as previously described [10, 20]. Briefly, pregnant rats were kept awake by gentle tapping or rattling of the cage and, if necessary, by gently being touched with a soft brush if behavioral signs of sleep were observed, such as closed eyes and immobility. Food and water were available ad libitum throughout the sleep deprivation period.
Reagents and antibodies
All drugs were purchased from Sigma-Aldrich. Mouse Anti-BrdU monoclonal antibody was purchased from Sigma-Aldrich. Rabbit anti-NeuN monoclonal antibody was purchased from Millipore. Rabbit anti-GFAP monoclonal was purchased from Abcam. Complete protease inhibitor cocktail tablets and phosphatase inhibitor cocktail tablets were purchased from Roche Applied Science.
Morris water maze
Spatial learning and memory were examined with the Morris water maze using programs similar to those described previously [21, 22]. Briefly, rats were trained in a circular fiberglass pool (180-cm diameter) over 4 trials per day for 6 consecutive days to find a hidden platform. During each trial, the rats that cannot find the hidden platform within 60 s were guided to the platform where they remained for 20 s. A probe test was performed 24 h after the last learning trial. All trials were recorded and analyzed by using an Any-maze tracking system (Stoelting, USA).
Elevated plus maze test
The plus maze apparatus consisted of two opposite open arms and two opposite closed arms (20-cm-tall walls on the closed arms) arranged at right angles. At the beginning of the test, rats were put in the center of the apparatus, which is elevated 1 m above the floor. The number of entries and the time spent in each arm were recorded for 10 min by ANY-maze video tracking system.
Novelty-suppressed feeding test
Novelty-suppressed feeding test was performed as described previously . In brief, rats were deprived of food for 48 h prior to the test. During test, a single pellet of food was placed on a white filter paper located in the center of the arena (60 × 60 cm), and rat was placed in a corner of the arena to explore the arena for 12 min. The latency to begin eating food and the amount of food consumption were recorded. The rats were immediately returned to their home cages after test, where food consumption was monitored for another 30 min.
Forced swimming test
Rats were forced to swim in a cylinder filled with water (temperature 24–25 °C; 20 cm in diameter, 40 cm in height) for 10 min. The latency to immobility and total immobility time were recorded and analyzed by using ANY-maze video tracking system.
To label newborn cells, rats were subjected to BrdU injection (100 mg/kg, i.p.) at age of 2 weeks or 6 weeks, and were sacrificed 4 weeks or 24 h after the last BrdU injection, respectively. The animals were deeply anesthetized and transcardially perfused with 4 % paraformaldehyde in 100 mM phosphate buffer, pH 7.4. Immunohistochemistry was performed on 30-μm coronal sections as previously described [23, 24]. Every sixth slice with the same reference position was stained. Positive cells were quantitated using a 40× objective (Leica). Obtaining numbers were multiplied by 6 to determine the estimated total number of positive cells per dentate gyrus (DG) of rat.
Electrophysiology in vivo
Rats were deeply anesthetized with sodium pentobarbital at a dose of 60 mg/kg (i.p.) and then mounted to a stereotaxic frame (Stoelting Co.). The core temperature was monitored and kept at 36.5 °C ± 0.5 °C. Stimulating and recording electrodes (a pair of 100 μm outer diameter Teflon-coated wires; A-M Systems Inc.) were located at the Schaffer collaterals of dorsal hippocampus and ipsilateral striatum radiatum of hippocampal CA1 area, respectively. Final positions of the electrodes were determined when an optimal response of field excitatory post-synaptic potential (fEPSP) was obtained. Baseline responses were recorded at 0.033 Hz for 30 min, with an intensity that evoked half of maximum amplitude. Once the stable baseline was obtained, a HFS consisted of 100 pulses at 100 Hz was delivered to induce LTP.
Electrophysiology in vitro
Rats were deeply anesthetized with 25 % urethane (1.5 g/kg, i.p.) and transcardially perfused with NMDG artificial cerebral spinal fluid (in mM: NMDG 93, HCl 93, KCl 2.5, NaH2PO4 1.2, CaCl2 0.5, MgSO4 10, NaHCO3 30, HEPES 20, Na-ascorbate 5.0, Na-pyruvate 3.0, Thiourea 2.0, NAC 12, and D-glucose 25, pH = 7.3.) prior to decapitation. The brain was rapidly dissected and placed in ice-cold NMDG ACSF. Hippocampal slices (400 μm) were coronally sectioned with a vibratome (VT1200S, Leica Microsystems, Bannockburn, IL) and then were incubated in HEPES ACSF (in mM: NaCl 92, KCl 2.5, NaH2PO4 1.2, CaCl2 0.5, MgSO4 10, NaHCO3 30, HEPES 20, Na-ascorbate 5.0, Na-pyruvate 3.0, Thiourea 2.0, NAC 12, and 25 D-glucose, pH = 7.3.) for 1 h at 30 °C.
Miniature excitatory postsynaptic currents (mEPSCs) of hippocampal CA1 pyramidal neurons were recorded with pipette filled with internal solution (in mM: Cs-methanesulfonate 130, MgCl2 2.0, EGTA 0.5, HEPES 10, QX-314 5.0, K2ATP 5.0, and Na2GTP 0.3, pH = 7.3), resistance of which was 3–5 MΩ. Bicuculline methiodide (10 μM) and TTX (1 μM) were added in ACSF (in mM: NaCl 120, KCl 2.5, NaH2PO4 1.25, CaCl2 2.0, MgSO4 2.0, NaHCO3 26, glucose 10, pH = 7.3) to block GABA receptors and Na+ channels respectively. Data acquisition (filtered at 3 kHz and digitized at 10 kHz) was performed with PatchMaster v2.73 (HEKA Electronic, Lambrecht/Pfalz, Germany) with holding potential at −70 mV. Mini Analysis Program 6.0.3 (Synaptosoft Inc., Decatur, GA) was used to automatically detected mEPSCs.
All data are presented as mean ± SEM. Spatial learning data were analyzed by a two-way ANOVA, with treatment (group) as the between-subjects factor and learning day as the within-subjects factor. All the other data were analyzed by a one-way ANOVA, with treatment (group) as the between-subjects factor. Significance level was set at p < 0.05.
Maternal sleep deprivation impairs spatial learning and memory in the offspring rats
Maternal sleep deprivation increases anxiety and depressive behaviors in the offspring rats
Taken together, these results indicate that maternal sleep deprivation increases anxiety and depression in the offspring rats.
Maternal sleep deprivation reduces adult hippocampal neurogenesis in the offspring rats
Thus, these results suggest that maternal sleep deprivation leads to a significant reduction in adult hippocampal neurogenesis including neuronal proliferation and survival in the offspring rats.
Maternal sleep deprivation impairs hippocampal LTP and basal synaptic transmission in the offspring rats
The physiological and biochemical changes of pregnancy may place women at risk for developing specific sleep disorders [3, 4]. Indeed, recent report shows that about two-thirds of the pregnant women are subjected to sleep disorders . Although it is widely accepted that maternal sleep restriction may lead to several harmful consequences to the offspring, human studies on sleep deprivation during pregnancy and the child’s development are difficult and even impossible to be conducted due to ethical and other issues. Therefore, the present study was designed to investigate the effects of maternal sleep deprivation by gentle handling in the rat model on cognitive and emotional functions in the offspring. Gentle handling protocols for sleep deprivation in animal models are widely used in research under laboratory conditions [10, 20], as it is a simple method for sleep deprivation .
Previous studies have shown that pregnancy-related hormones such as progesterone, estrogen, cortisol and oxytocin are gradually increased during pregnancy, especially in the third trimester of gestation, which markedly affect sleep quality . Thus, a large number of reports have focused on the influence of sleep deprivation during the last trimester of pregnancy on the development of the offspring [7, 9, 10, 28, 29]. Recently, a report shows that paradoxical sleep deprivation using the multiple platform method at different pregnant period impairs hippocampus-dependent spatial learning and memory in the young offspring rats . In full agreement with this finding, we here reported that maternal sleep deprivation through the gentle handling method at the different stages of pregnancy displayed a similar deficit in spatial learning and memory, especially for the first 3 days of learning in the Morris water maze task (Fig. 1), suggesting a delayed acquisition of spatial memory in the offspring rats. In addition, Gulia and colleagues have recently reported that pups born to sleep deprived mothers displayed a decrease in ultrasonic vocalizations , indicating a depressive-like symptom. Consistent with this result, we here found that rats born to mothers undergoing sleep deprivation displayed apparently depression during forced-swimming test (Fig. 2). However, we also found that maternal sleep deprivation significantly induced anxiety-like behaviors in the offspring in both elevated-plus maze and novelty-suppressed feeding tests (Fig. 3 and Fig. 4), which is not consistent with a previous report that sleep deprivation during late pregnancy produces a decrease in anxiety-related behavior, as reflected by hyperactivity and increased risk-taking behavior in the offspring . Given this controversy, further studies are required to determine the exact reason for the different results.
Although our findings, along with evidence accumulated from previous studies [6, 7], reveal that sufficient sleep at any stage of pregnancy is critical for the development of cognitive and emotional functions in the offspring, how maternal sleep deprivation disrupts cognitive and emotional functions in the offspring remains poorly understood. Consistent with recent reports [6, 7], we here confirmed that maternal sleep deprivation resulted in a dramatic decrease in the number of newborn neurons in the DG of the hippocampal formation (Fig. 5 and Fig. 6). Although the function of adult neurogenesis is still under debate, integration of newborn neurons into the existing neuronal circuits may be involved in memory processing and emotional regulation in the hippocampus [30, 31]. Thus, the inhibition of hippocampal neurogenesis induced by maternal sleep deprivation in the present study may contribute to the impairment of hippocampus-dependent spatial learning and memory as well as the increase in depression and anxiety in the offspring. In addition, more recent study has proposed that maternal sleep deprivation may lead to dysregulation in microglial pro- and anti-inflammatory activation, and consequently inhibit adult hippocampal neurogenesis and impair hippocampal-dependent spatial learning and memory, as anti-inflammatory treatment can relief cognitive impairment caused by maternal sleep deprivation in offspring. . Furthermore, activity-dependent hippocampal synaptic plasticity such as LTP has been considered as a cellular mechanism underlying information processing and memory formation [15–17]. We therefore speculate that maternal sleep deprivation may impair hippocampal LTP induction, and subsequently leads to memory deficit in the young offspring rats. Indeed, we here found that both hippocampal LTP (Fig. 7) and basal synaptic transmission (Fig. 8) were significantly suppressed in the young offspring rats born to mothers undergoing sleep deprivation during pregnancy, which may contribute, at least partially, to the disruption of cognitive and emotional functions.
Notably, although we used gentle handling that minimizes stress , to perform maternal sleep deprivation, it may still be a stressful procedure. It has been documented that maternal stress produces memory deficits and hippocampal synaptic plasticity impairment in the offspring [33–36]. Thus, the effects of acute stress resulting from sleep deprivation on cognitive and emotional functions in the young offspring rats cannot be occluded in the present study. Additionally, maternal sleep deprivation during their inactive phase may lead to sleep compensation during their active phase. Previous studies have shown that phase-shifting circadian rhythms may influence hippocampus-dependent memory [37, 38]. Thus, maternal sleep deprivation may result in the disruption of circadian rhythms, and subsequently contributes to memory deficits in the offspring.
Although our results show that maternal sleep deprivation suppresses hippocampal neurogenesis and synaptic plasticity that may contribute to memory deficits in the young offspring rats, the exact mechanism still remains unclear. Further research is needed to enhance our understanding of the effect of maternal sleep deprivation on offspring development and the physiological mechanisms underlying this influence.
Overall, our study shows that maternal sleep deprivation at different stages of pregnancy leads to a significant increase in depression and anxiety, and dramatic deficits in spatial learning and memory. These behavioral changes are associated with the impairments of excitatory synaptic transmission and LTP in the hippocampus.
This work was supported by the 973 Program of the Ministry of Science and Technology of China (2014CB548100), the National Natural Science Foundation of China (81271221, 81400874, 81571042 and 81501143), the Natural Science Foundation of Chongqing (cstc2015jcyjA00037), the China Postdoctoral Science Foundation (2014M562505XB) and the Chongqing Postdoctoral Foundation (xm2014051).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Rechtschaffen A, Bergmann BM, Everson CA, Kushida CA, Gilliland MA. Sleep deprivation in the rat: X. Integration and discussion of the findings. Sleep. 1989;12(1):68–87.PubMedGoogle Scholar
- WHO. Worldwide project on sleep and health. WHO/MSA/MND. 1998;98.3:1–12.Google Scholar
- Mindell JA, Jacobson BJ. Sleep disturbances during pregnancy. J Obstet Gynecol Neonatal Nurs. 2000;29(6):590–7.View ArticlePubMedGoogle Scholar
- Pien GW, Schwab RJ. Sleep disorders during pregnancy. Sleep. 2004;27(7):1405–17.PubMedGoogle Scholar
- Ross LE, Murray BJ, Steiner M. Sleep and perinatal mood disorders: a critical review. J Psychiatry Neurosci. 2005;30(4):247–56.PubMed CentralPubMedGoogle Scholar
- Zhao Q, Peng C, Wu X, Chen Y, Wang C, You Z. Maternal sleep deprivation inhibits hippocampal neurogenesis associated with inflammatory response in young offspring rats. Neurobiol Dis. 2014;68:57–65.View ArticlePubMedGoogle Scholar
- Zhao Q, Xie X, Fan Y, Zhang J, Jiang W, Wu X, Yan S, Chen Y, Peng C, You Z. Phenotypic dysregulation of microglial activation in young offspring rats with maternal sleep deprivation-induced cognitive impairment. Sci Rep. 2015;5:9513.Google Scholar
- Alvarenga TA, Aguiar MF, Mazaro-Costa R, Tufik S, Andersen ML. Effects of sleep deprivation during pregnancy on the reproductive capability of the offspring. Fertil Steril. 2013;100(6):1752–7.View ArticlePubMedGoogle Scholar
- Gulia KK, Patel N, Kumar VM. Increased ultrasonic vocalizations and risk-taking in rat pups of sleep-deprived dams. Physiol Behav. 2015;139:59–66.View ArticlePubMedGoogle Scholar
- Radhakrishnan A, Aswathy BS, Kumar VM, Gulia KK. Sleep deprivation during late pregnancy produces hyperactivity and increased risk-taking behavior in offspring. Brain Res. 2015;1596:88–98.View ArticlePubMedGoogle Scholar
- Gulia KK, Patel N, Radhakrishnan A, Kumar VM. Reduction in ultrasonic vocalizations in pups born to rapid eye movement sleep restricted mothers in rat model. PLoS One. 2014;9(1), e84948.PubMed CentralView ArticlePubMedGoogle Scholar
- Guzman-Marin R, Suntsova N, Methippara M, Greiffenstein R, Szymusiak R, McGinty D. Sleep deprivation suppresses neurogenesis in the adult hippocampus of rats. Eur J Neurosci. 2005;22(8):2111–6.View ArticlePubMedGoogle Scholar
- Mirescu C, Peters JD, Noiman L, Gould E. Sleep deprivation inhibits adult neurogenesis in the hippocampus by elevating glucocorticoids. Proc Natl Acad Sci U S A. 2006;103(50):19170–5.PubMed CentralView ArticlePubMedGoogle Scholar
- Sportiche N, Suntsova N, Methippara M, Bashir T, Mitrani B, Szymusiak R, McGinty D. Sustained sleep fragmentation results in delayed changes in hippocampal-dependent cognitive function associated with reduced dentate gyrus neurogenesis. Neuroscience. 2010;170(1):247–58.Google Scholar
- Bliss TV, Collingridge GL. A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 1993;361(6407):31–9.View ArticlePubMedGoogle Scholar
- Collingridge GL, Peineau S, Howland JG, Wang YT. Long-term depression in the CNS. Nat Rev Neurosci. 2010;11(7):459–73.View ArticlePubMedGoogle Scholar
- Malenka RC, Nicoll RA. Long-term potentiation--a decade of progress? Science. 1999;285(5435):1870–4.View ArticlePubMedGoogle Scholar
- Martin SJ, Grimwood PD, Morris RG. Synaptic plasticity and memory: an evaluation of the hypothesis. Annu Rev Neurosci. 2000;23:649–711.View ArticlePubMedGoogle Scholar
- Campbell IG, Guinan MJ, Horowitz JM. Sleep deprivation impairs long-term potentiation in rat hippocampal slices. J Neurophysiol. 2002;88(2):1073–6.PubMedGoogle Scholar
- Vecsey CG, Baillie GS, Jaganath D, Havekes R, Daniels A, Wimmer M, Huang T, Brown KM, Li XY, Descalzi G et al. Sleep deprivation impairs cAMP signalling in the hippocampus. Nature. 2009;461(7267):1122–5.Google Scholar
- Dong Z, Bai Y, Wu X, Li H, Gong B, Howland JG, Huang Y, He W, Li T, Wang YT. Hippocampal long-term depression mediates spatial reversal learning in the Morris water maze. Neuropharmacology. 2013;64:65–73.Google Scholar
- Wang W, Tan T, Tu M, He W, Dong Z, Han H. Acute pentobarbital treatment impairs spatial learning and memory and hippocampal long-term potentiation in rats. Physiol Behav. 2015;149:169–73.View ArticlePubMedGoogle Scholar
- Wu X, Bai Y, Tan T, Li H, Xia S, Chang X, Zhou Z, Zhou W, Li T, Wang YT et al. Lithium ameliorates autistic-like behaviors induced by neonatal isolation in rats. Front Behav Neurosci. 2014;8:234.Google Scholar
- Dong Z, Han H, Li H, Bai Y, Wang W, Tu M, Peng Y, Zhou L, He W, Wu X et al. Long-term potentiation decay and memory loss are mediated by AMPAR endocytosis. J Clin Invest. 2015;125(1):234–47.Google Scholar
- Lopes EA, Carvalho LB, Seguro PB, Mattar R, Silva AB, Prado LB, Prado GF. Sleep disorders in pregnancy. Arq Neuropsiquiatr. 2004;62(2A):217–21.Google Scholar
- Rechtschaffen A, Bergmann BM, Gilliland MA, Bauer K. Effects of method, duration, and sleep stage on rebounds from sleep deprivation in the rat. Sleep. 1999;22(1):11–31.PubMedGoogle Scholar
- Bourjeily G. Sleep disorders in pregnancy. Obstetric Medicine. 2009;2:100–6.View ArticleGoogle Scholar
- Khalyfa A, Mutskov V, Carreras A, Khalyfa AA, Hakim F, Gozal D. Sleep fragmentation during late gestation induces metabolic perturbations and epigenetic changes in adiponectin gene expression in male adult offspring mice. Diabetes. 2014;63(10):3230–41.PubMed CentralView ArticlePubMedGoogle Scholar
- Micheli K, Komninos I, Bagkeris E, Roumeliotaki T, Koutis A, Kogevinas M, Chatzi L. Sleep patterns in late pregnancy and risk of preterm birth and fetal growth restriction. Epidemiology. 2011;22(5):738–44.Google Scholar
- Meerlo P, Mistlberger RE, Jacobs BL, Heller HC, McGinty D. New neurons in the adult brain: the role of sleep and consequences of sleep loss. Sleep Med Rev. 2009;13(3):187–94.PubMed CentralView ArticlePubMedGoogle Scholar
- Novati A, Hulshof HJ, Koolhaas JM, Lucassen PJ, Meerlo P. Chronic sleep restriction causes a decrease in hippocampal volume in adolescent rats, which is not explained by changes in glucocorticoid levels or neurogenesis. Neuroscience. 2011;190:145–55.View ArticlePubMedGoogle Scholar
- Ledoux L, Sastre JP, Buda C, Luppi PH, Jouvet M. Alterations in c-fos expression after different experimental procedures of sleep deprivation in the cat. Brain Res. 1996;735(1):108–18.View ArticlePubMedGoogle Scholar
- Benoit JD, Rakic P, Frick KM. Prenatal stress induces spatial memory deficits and epigenetic changes in the hippocampus indicative of heterochromatin formation and reduced gene expression. Behav Brain Res. 2015;281:1–8.View ArticlePubMedGoogle Scholar
- Modir F, Elahdadi Salmani M, Goudarzi I, Lashkarboluki T, Abrari K. Prenatal stress decreases spatial learning and memory retrieval of the adult male offspring of rats. Physiol Behav. 2014;129:104–9.View ArticlePubMedGoogle Scholar
- Son GH, Geum D, Chung S, Kim EJ, Jo JH, Kim CM, Lee KH, Kim H, Choi S, Kim HT et al. Maternal stress produces learning deficits associated with impairment of NMDA receptor-mediated synaptic plasticity. J Neurosci. 2006;26(12):3309–18.Google Scholar
- Yang J, Han H, Cao J, Li L, Xu L. Prenatal stress modifies hippocampal synaptic plasticity and spatial learning in young rat offspring. Hippocampus. 2006;16(5):431–6.View ArticlePubMedGoogle Scholar
- Devan BD, Goad EH, Petri HL, Antoniadis EA, Hong NS, Ko CH, Leblanc L, Lebovic SS, Lo Q, Ralph MR et al. Circadian phase-shifted rats show normal acquisition but impaired long-term retention of place information in the water task. Neurobiol Learn Mem. 2001;75(1):51–62.Google Scholar
- Valentinuzzi VS, Kolker DE, Vitaterna MH, Ferrari EA, Takahashi JS, Turek FW. Effect of circadian phase on context and cued fear conditioning in C57BL/6 J mice. Animal Learn Behav. 2001;29(2):133–42.View ArticleGoogle Scholar