TY - JOUR
T1 - Interleukin-1β enhances susceptibility to hyperthermia-induced seizures in developing rats
AU - Fukuda, Mitsumasa
AU - Suzuki, Yuka
AU - Ishizaki, Yoshito
AU - Kira, Ryutaro
AU - Kikuchi, Chiya
AU - Watanabe, Shohei
AU - Hino, Hitomi
AU - Morimoto, Takehiko
AU - Hara, Toshiro
AU - Ishii, Eiichi
PY - 2009/4
Y1 - 2009/4
N2 - Cytokines have been shown to influence susceptibility to febrile seizures and epilepsy. In this study, the role of interleukin-1β (IL-1β) was examined in developing rats. IL-1β and interleukin-1 receptor antagonist (IL-1ra) were administered to developing rats, and seizures were induced by moist warm air. Twenty male Lewis rats (21-23 days old) were divided into two groups (IL-1β and saline control groups) and two holes were made in the skull for EEG electrodes. We applied human recombinant IL-1β intra-nasally 1 h before seizures induced by moist warm air. The brain temperature at the appearance of seizure discharges on EEG, and the latency time from the hyperthermia onset until the appearance of seizure discharges on EEG were measured. And the same study using IL-1ra was performed. The median brain temperature for the IL-1β group, 42.6 °C (range: 41.8-43.0), was significantly lower than that for the control, 42.9 (42.3-43.4) (P = 0.043). The brain temperature for the IL-1ra group, 43.3 (42.8-43.7), was significantly higher than that for the control, 42.9 (42.2-43.5) (P = 0.011), and the latency time for the IL-1ra group, 398 s (270-561), was significantly longer than that for the control, 325 (252-462) (P = 0.035). These results demonstrate that IL-1β promotes hyperthermia-induced seizures in developing rats.
AB - Cytokines have been shown to influence susceptibility to febrile seizures and epilepsy. In this study, the role of interleukin-1β (IL-1β) was examined in developing rats. IL-1β and interleukin-1 receptor antagonist (IL-1ra) were administered to developing rats, and seizures were induced by moist warm air. Twenty male Lewis rats (21-23 days old) were divided into two groups (IL-1β and saline control groups) and two holes were made in the skull for EEG electrodes. We applied human recombinant IL-1β intra-nasally 1 h before seizures induced by moist warm air. The brain temperature at the appearance of seizure discharges on EEG, and the latency time from the hyperthermia onset until the appearance of seizure discharges on EEG were measured. And the same study using IL-1ra was performed. The median brain temperature for the IL-1β group, 42.6 °C (range: 41.8-43.0), was significantly lower than that for the control, 42.9 (42.3-43.4) (P = 0.043). The brain temperature for the IL-1ra group, 43.3 (42.8-43.7), was significantly higher than that for the control, 42.9 (42.2-43.5) (P = 0.011), and the latency time for the IL-1ra group, 398 s (270-561), was significantly longer than that for the control, 325 (252-462) (P = 0.035). These results demonstrate that IL-1β promotes hyperthermia-induced seizures in developing rats.
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U2 - 10.1016/j.seizure.2008.10.001
DO - 10.1016/j.seizure.2008.10.001
M3 - Article
C2 - 19004647
AN - SCOPUS:61349159237
SN - 1059-1311
VL - 18
SP - 211
EP - 214
JO - Seizure : the journal of the British Epilepsy Association
JF - Seizure : the journal of the British Epilepsy Association
IS - 3
ER -