Opp M R, Krueger J M
Department of Physiology and Biophysics, University of Tennessee, Memphis 38163.
Am J Physiol. 1991 Feb;260(2 Pt 2):R453-7. doi: 10.1152/ajpregu.1991.260.2.R453.
The recent purification and characterization of an interleukin 1-receptor antagonist (IL-1ra) has provided an additional means of elucidating the mechanisms involved in the responses initiated by IL-1. Central administration of IL-1 to rabbits results in a characteristic febrile response and in increased non-rapid-eye-movement sleep (NREMS). In this study, rabbits received various doses of IL-1ra (10-1,000 micrograms) or pyrogen-free saline intracerebroventricularly, and sleep-wake activity and brain temperature (Tbr) were determined for the next 24 h. All doses of IL-1ra tested tended to reduce NREMS in the first postinjection hour with little effect on Tbr. When rabbits were pretreated with 100 micrograms IL-1ra and then injected with 10 ng IL-1, the characteristic IL-1-induced febrile and NREMS-promoting effects were completely blocked.
白细胞介素-1受体拮抗剂(IL-1ra)最近的纯化和特性鉴定为阐明IL-1引发的反应机制提供了额外的手段。向兔子脑内注射IL-1会导致典型的发热反应和非快速眼动睡眠(NREMS)增加。在本研究中,兔子脑室内注射不同剂量的IL-1ra(10 - 1000微克)或无热原生理盐水,然后在接下来的24小时内测定睡眠-觉醒活动和脑温(Tbr)。所测试的所有剂量的IL-1ra在注射后的第一个小时内都倾向于减少NREMS,而对Tbr影响很小。当兔子预先用100微克IL-1ra处理,然后注射10纳克IL-1时,IL-1诱导的典型发热和促进NREMS的作用被完全阻断。