TY - JOUR
T1 - An interleukin-1 receptor fragment blocks ambient temperature-induced increases in brain temperature but not sleep in rabbits
AU - Kushikata, Tetsuya
AU - Takahashi, Satoshi
AU - Wang, Ying
AU - Fang, Jidong
AU - Krueger, James M.
N1 - Funding Information:
This work was supported by the National Institutes of Health (National Institute of Neurological Diseases and Stroke, NS25378 and NS31453).
PY - 1998/3/20
Y1 - 1998/3/20
N2 - The effects of intracerebroventricular injection (i.c.v.) of an interleukin-1 (IL-1) inhibitor, a soluble IL-1 receptor fragment (IL-1RF), on sleep and brain temperature (T(br)) responses of rabbits induced by mild increases in ambient temperature (T(amb)) were determined. Each rabbit was recorded under three conditions: (1) 21°C T(amb) plus pyrogen-free saline (PFS); (2) 27°C T(amb) plus PFS; (3) 27°C T(amb) plus the IL-1RF. The higher T(amb) significantly increased T(br) during the warming period; this effect was attenuated by pretreatment with the IL-1RF. The higher T(amb) alone (6 h exposure) significantly increased non-rapid eye movement sleep (NREMS) across the 23-h recording period. However, during the 6-h warming period NREMS values, obtained after IL-1RF treatment, were not significantly different from those obtained from PFS-treated animals at 27°C T(amb). The ability of the IL-1RF to block T(amb)-induced changes in T(br) and the failure of the IL-1RF to block T(amb)-induced NREMS responses is different from previous results which indicated that a tumor necrosis factor receptor fragment (TNF-RF) inhibits warm T(amb)-induced sleep but not T(br) responses. Thus, brain IL-1 and TNF sleep and thermo mechanisms are, in part, different.
AB - The effects of intracerebroventricular injection (i.c.v.) of an interleukin-1 (IL-1) inhibitor, a soluble IL-1 receptor fragment (IL-1RF), on sleep and brain temperature (T(br)) responses of rabbits induced by mild increases in ambient temperature (T(amb)) were determined. Each rabbit was recorded under three conditions: (1) 21°C T(amb) plus pyrogen-free saline (PFS); (2) 27°C T(amb) plus PFS; (3) 27°C T(amb) plus the IL-1RF. The higher T(amb) significantly increased T(br) during the warming period; this effect was attenuated by pretreatment with the IL-1RF. The higher T(amb) alone (6 h exposure) significantly increased non-rapid eye movement sleep (NREMS) across the 23-h recording period. However, during the 6-h warming period NREMS values, obtained after IL-1RF treatment, were not significantly different from those obtained from PFS-treated animals at 27°C T(amb). The ability of the IL-1RF to block T(amb)-induced changes in T(br) and the failure of the IL-1RF to block T(amb)-induced NREMS responses is different from previous results which indicated that a tumor necrosis factor receptor fragment (TNF-RF) inhibits warm T(amb)-induced sleep but not T(br) responses. Thus, brain IL-1 and TNF sleep and thermo mechanisms are, in part, different.
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U2 - 10.1016/S0304-3940(98)00152-9
DO - 10.1016/S0304-3940(98)00152-9
M3 - Article
C2 - 9593505
AN - SCOPUS:0032549716
SN - 0304-3940
VL - 244
SP - 125
EP - 128
JO - Neuroscience letters
JF - Neuroscience letters
IS - 3
ER -