TY - JOUR
T1 - Cytokines in sleep regulation
AU - Krueger, James M.
AU - Takahashi, Satoshi
AU - Kapás, Levente
AU - Bredow, Sebastian
AU - Roky, Rachida
AU - Fang, Jidong
AU - Floyd, Rachael
AU - Renegar, Kathryn B.
AU - Guha-Thakurta, Nandita
AU - Novitsky, Sergei
AU - Obál, Ferenc
N1 - Funding Information:
This work was supported, in part, by the Office of Naval Research (N00014-90-J-1069) and the National Institutes of Health (NS-25378, NS-27250, NS-31453 and NS-30514).
PY - 1995
Y1 - 1995
N2 - The central thesis of this essay is that the cytokine network in brain is a key element in the humoral regulation of sleep responses to infection and in the physiological regulation of sleep. We hypothesize that many cytokines, their cellular receptors, soluble receptors, and endogenous antagonists are involved in physiological sleep regulation. The expressions of some cytokines are greatly amplified by microbial challenge. This excess cytokine production during infection induces sleep responses. The excessive sleep and wakefulness that occur at different times during the course of the infectious process result from dynamic changes in various cytokines that occur during the host's response to infectious challenge. Removal of any one somnogenic cytokine inhibits normal sleep, alters the cytokine network by changing the cytokine mix, but does not completely disrupt sleep due to the redundant nature of the cytokine network. The cytokine network operates in a paracrine/autocrine fashion and is responsive to neuronal use. Finally, cytokines elicit their somnogenic actions via endocrine and neurotransmitter systems as well as having direct effects on neurons and glia. Evidence in support of these postulates is reviewed in this essay.
AB - The central thesis of this essay is that the cytokine network in brain is a key element in the humoral regulation of sleep responses to infection and in the physiological regulation of sleep. We hypothesize that many cytokines, their cellular receptors, soluble receptors, and endogenous antagonists are involved in physiological sleep regulation. The expressions of some cytokines are greatly amplified by microbial challenge. This excess cytokine production during infection induces sleep responses. The excessive sleep and wakefulness that occur at different times during the course of the infectious process result from dynamic changes in various cytokines that occur during the host's response to infectious challenge. Removal of any one somnogenic cytokine inhibits normal sleep, alters the cytokine network by changing the cytokine mix, but does not completely disrupt sleep due to the redundant nature of the cytokine network. The cytokine network operates in a paracrine/autocrine fashion and is responsive to neuronal use. Finally, cytokines elicit their somnogenic actions via endocrine and neurotransmitter systems as well as having direct effects on neurons and glia. Evidence in support of these postulates is reviewed in this essay.
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U2 - 10.1016/0960-5428(95)00007-O
DO - 10.1016/0960-5428(95)00007-O
M3 - Article
C2 - 7496611
AN - SCOPUS:0029146123
SN - 0960-5428
VL - 5
SP - 171
EP - 188
JO - Advances in Neuroimmunology
JF - Advances in Neuroimmunology
IS - 2
ER -