J Korean Soc Emerg Med.  2012 Jun;23(3):411-419.

Appropriate Rest Time after Repetitive Sleep Deprivation Suppresses Apoptosis and Cell Proliferation in the Hippocampus

Affiliations
  • 1Department of Physiology, College of Medicine, Kyung Hee University, Seoul, Korea.
  • 2Department of Internal Medicine, AndongSungso Hospital, Gyeongbuk, Korea.
  • 3Department of Physical Therapy, Kyungnam University, Gyeongnam, Korea.
  • 4Department of Emergency Medicine, College of Medicine, Kyung Hee University, Seoul, Korea.
  • 5Department of Emergency Medicine, Korea University College of Medicine, Ansan Hospital, Ansan, Korea. chohj327@hotmail.com

Abstract

PURPOSE
Sleep deprivation may exert many negative effects on hippocampus-dependent cognitive function, such as learning and memory. The present study was conducted in order to investigate the effects of repetitive sleep deprivation on cognition, apoptotic neuronal cell death, and cell proliferation in the hippocampus, using mice.
METHODS
To induce sleep deprivation, mice were placed in a water cage containing six platforms (3 cm in diameter), surrounded by water up to 1 cm beneath the surface of the platform for 24 h. Mice were randomly divided into four groups (n=20 in each group): control group, 24 h rest after 24 h sleep deprivation group, 48 h rest after 24 h sleep deprivation group, and 72 h rest after 24 h sleep deprivation group. This cycle was continued for 36 days. Novel objective recognition test and immunohistochemistry for 5-bromo-2'-deoxyuridine (BrdU), western blot for expression of Bax, Bcl-2, brain-derived neurotrophic factor (BDNF), and caspase-3 were performed.
RESULTS
Results of the novel objective recognition test showed decreased cognition in the 24 h rest after 24 h sleep deprivation group, while a similar effect was observed in other groups, compared to the control group. Increased cell proliferation and enhanced expression of BDNF and Bax protein were observed in the 24 h rest after 24 h sleep deprivation group and the 48 h rest after 24 h sleep deprivation group, compared to the control group. Expression of Bcl-2 showed a decrease in the 24 h and 48 h rest groups, compared to the control group. Expression of caspase-3 in the dentate gyrus of the hippocampus showed a significant increase in the 24 h rest after 24 h sleep deprivation group and in the 48 h rest after 24 h sleep deprivation group, compared to the control group.
CONCLUSION
Results of the present study indicate that insufficient rest after sleep deprivation may induce impairment of cognitive function. After sleep deprivation, at least 72 hr of rest time is needed for recovery.

Keyword

Sleep deprivation; Short-term memory; Hippocampus; Apoptosis; Cell proliferation

MeSH Terms

Animals
Apoptosis
bcl-2-Associated X Protein
Blotting, Western
Brain-Derived Neurotrophic Factor
Bromodeoxyuridine
Caspase 3
Cell Death
Cell Proliferation
Cognition
Dentate Gyrus
Hippocampus
Immunohistochemistry
Learning
Memory
Memory, Short-Term
Mice
Neurons
Sleep Deprivation
Water
Brain-Derived Neurotrophic Factor
Bromodeoxyuridine
Caspase 3
Water
bcl-2-Associated X Protein
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