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5′‐Ectonucleotidase‐knockout mice lack non‐REM sleep responses to sleep deprivation
Author(s) -
Zielinski Mark R.,
Taishi Ping,
Clinton James M.,
Krueger James M.
Publication year - 2012
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2012.08112.x
Subject(s) - adenosine , extracellular , sleep deprivation , endocrinology , knockout mouse , medicine , sleep (system call) , adenosine triphosphate , adenosine monophosphate , rapid eye movement sleep , wakefulness , biology , chemistry , neuroscience , biochemistry , circadian rhythm , receptor , electroencephalography , computer science , operating system
Adenosine and extracellular adenosine triphosphate (ATP) have multiple physiological central nervous system actions including regulation of cerebral blood flow, inflammation and sleep. However, their exact sleep regulatory mechanisms remain unknown. Extracellular ATP and adenosine diphosphate are converted to adenosine monophosphate (AMP) by the enzyme ectonucleoside triphosphate diphosphohydrolase 1, also known as CD39, and extracellular AMP is in turn converted to adenosine by the 5′‐ectonuleotidase enzyme CD73. We investigated the role of CD73 in sleep regulation. Duration of spontaneous non‐rapid eye movement sleep (NREMS) was greater in CD73‐knockout (KO) mice than in C57BL/6 controls whether determined in our laboratory or by others. After sleep deprivation (SD), NREMS was enhanced in controls but not CD73‐KO mice. Interleukin‐1 beta (IL1β) enhanced NREMS in both strains, indicating that the CD73‐KO mice were capable of sleep responses. Electroencephalographic power spectra during NREMS in the 1.0–2.5 Hz frequency range was significantly enhanced after SD in both CD73‐KO and WT mice; the increases were significantly greater in the WT mice than in the CD73‐KO mice. Rapid eye movement sleep did not differ between strains in any of the experimental conditions. With the exception of CD73 mRNA, the effects of SD on various adenosine‐related mRNAs were small and similar in the two strains. These data suggest that sleep is regulated, in part, by extracellular adenosine derived from the actions of CD73.