Adenosine and sleep

Abstract 

Adenosine is directly linked to the energy metabolism of cells. In the central nervous system an increase in neuronal activity enhances energy consumption as well as extracellular adenosine concentrations. In most brain areas high extracellular adenosine concentrations, through A₁ adenosine receptors, decrease neuronal activity and thus the need for energy. Adenosine seems to act as a direct negative feed-back inhibitor of neuronal activity. Hypoxia and ischemia induce very high extracellular adenosine levels, which may limit further brain damage. In brain areas that regulate cortical vigilance, particularly in the basal forebrain, high extracellular adenosine concentrations, induced by prolonged wakefulness, decrease the activity of presumably cholinergic cells and via this mechanism promote sleep. Our hypothesis is that in the cholinergic basal forebrain prolonged wakefulness induces local energy depletion that generates increases in extracellular adenosine concentrations in this area.

In addition to the immediate effects, high extracellular adenosine concentrations also induce intracellular changes in signal transduction and transcription, e.g. increase in A₁ receptor expression and NF-κB binding activity. These changes may at least partially mediate the long term effects of prolonged wakefulness. Adenosine may also be a common mediator of the effects of several other sleep-inducing factors.

Keywords: adenosine, caffeine, c-fos, energy metabolism, NF-κB sleep, sleep deprivation

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• f1 Correspondence should be addressed to: Tarja Porkka-Heiskanen, Institute of Biomedicine, Department of Physiology, Biomedicum Helsinki, PO Box 63, 00014 University of Helsinki, Helsinki, Finland. Tel.: 191 25 317; Fax: 191 25 302; E-mail:porkka@cc.helsinki.fi