Obál F, Fang J, Payne L C, Krueger J M
Department of Physiology, A. Szent-Györgyi Medical School, Szeged, Hungary.
Neuroendocrinology. 1995 May;61(5):559-65. doi: 10.1159/000126880.
The involvement of endogenous growth-hormone-releasing hormone (GHRH) in the sleep-promoting activity of interleukin-1 (IL1) was studied. The effects on sleep of intracerebroventricular injection of IL1 were tested in rats pretreated with intracerebroventricular antibodies to GHRH (GHRH-ab). One group of rats received two treatments each consisting of two injections, control IgG + physiological saline (IgG + Sal) and on another day GHRH-ab + Sal, whereas another group of rats received IgG + Sal, IgG + IL1 and GHRH-ab + IL1 on separate days with one day off between the various treatments. IgG or GHRH-ab was injected 6 h prior to dark onset; Sal or IL1 was administered at dark onset. Recording of sleep-wake activity and cortical brain temperature (Tcrt) was started with the injection of IgG or GHRH-ab and continued for 18 h. GHRH-ab (GHRH-ab + Sal) suppressed rapid eye movement sleep (REMS), non-REMS (NREMS) and EEG slow-wave activity (SWA) during NREMS throughout the recording period. IL1 treatment (IgG + IL1) enhanced NREMS and SWA, and induced fever for 6 h. Pretreatment with GHRH-ab (GHRH-ab + IL1) abolished the IL1-induced increases in NREMS, attenuated the enhancements in SWA, and suppressed fever for 6 hours after IL1. The results indicate that the sleep-promoting activity of IL1 is mediated at least in part via GHRH. The suppression of the IL1-induced fever by GHRH-ab might be attributed to an inhibition of hypothalamic somatostatin.
研究了内源性生长激素释放激素(GHRH)在白细胞介素-1(IL1)促进睡眠活性中的作用。在脑室注射抗GHRH抗体(GHRH-ab)预处理的大鼠中,测试脑室注射IL1对睡眠的影响。一组大鼠接受两种处理,每种处理包括两次注射,即对照IgG +生理盐水(IgG + Sal),另一天为GHRH-ab + Sal,而另一组大鼠在不同日期接受IgG + Sal、IgG + IL1和GHRH-ab + IL1,各处理之间间隔一天。在黑暗开始前6小时注射IgG或GHRH-ab;在黑暗开始时给予Sal或IL1。从注射IgG或GHRH-ab开始记录睡眠-觉醒活动和皮质脑温(Tcrt),并持续18小时。在整个记录期间,GHRH-ab(GHRH-ab + Sal)抑制快速眼动睡眠(REMS)、非快速眼动睡眠(NREMS)以及NREMS期间的脑电图慢波活动(SWA)。IL1处理(IgG + IL1)增强了NREMS和SWA,并引起6小时的发热。用GHRH-ab预处理(GHRH-ab + IL1)消除了IL1诱导的NREMS增加,减弱了SWA的增强,并在IL1后6小时抑制了发热。结果表明,IL1促进睡眠的活性至少部分是通过GHRH介导的。GHRH-ab对IL1诱导的发热的抑制可能归因于对下丘脑生长抑素的抑制。