Proinflammatory cytokines, including interleukin-1 beta (IL-1 beta) and tum
or necrosis factor-alpha (TNF-alpha) are involved in sleep regulation. IL-1
0 is an anti-inflammatory cytokine that inhibits proinflammatory cytokine p
roduction. We hypothesized that IL-10 could attenuate sleep. Thirty-one mal
e rabbits were used. Three doses of IL-10 (5 ng, 50 ng, and 250 ng) were in
jected intracerebroventricularly during the rest (light) period. One dose o
f IL-10 (250, ng) was injected during the active (dark) cycle. Appropriate
time-matched control injections of saline were given to the same rabbits on
different days. The two highest doses of IL-10 significantly inhibited spo
ntaneous nonrapid eye movement sleep if IL-10 was given during the light cy
cle. The highest dose of IL-10 (250 ng) also significantly decreased rapid
eye movement sleep. IL-10 administered at dark onset had no effect on sleep
. The sleep inhibitory properties of IL-10 provide additional evidence for
the hypothesis that a br;tin cytokine network is involved in regulation of
physiologic sleep.