Nguyen K T, Deak T, Owens S M, Kohno T, Fleshner M, Watkins L R, Maier S F
Department of Psychology, University of Colorado at Boulder, Boulder, Colorado 80309, USA.
J Neurosci. 1998 Mar 15;18(6):2239-46. doi: 10.1523/JNEUROSCI.18-06-02239.1998.
Peripheral immune stimulation such as that provided by lipopolysaccharide (LPS) has been reported to increase brain levels of IL-1beta mRNA, immunoreactivity, and bioactivity. Stressors produce many of the same neural and endocrine responses as those that follow LPS, but the impact of stressors on brain interleukin-1beta (IL-1beta) has not been systematically explored. An ELISA designed to detect IL-1beta was used to measure levels of IL-1beta protein in rat brain. Brain IL-1beta was explored after exposure to inescapable shock (IS; 100 1.6 mA tail shocks for 5 sec each) and LPS (1 mg/kg) as a positive control. Rats were killed either immediately or 2, 7, 24, or 48 hr after IS. Brains were dissected into hypothalamus, hippocampus, cerebellum, posterior cortex, and nucleus tractus solitarius regions. LPS produced widespread increases in brain IL-1beta, but IS did not. Adrenal glucocorticoids are known to suppress IL-1beta production in both the periphery and brain. Thus, it was possible that the stressor did provide stimulus input to the brain IL-1beta system(s), but that the production of IL-1beta protein was suppressed by the rapid and prolonged high levels of glucocorticoids produced by IS. To test this possibility rats were adrenalectomized or given sham surgery, with half of the adrenalectomized rats receiving corticosterone replacement to maintain basal corticosterone levels. IS produced large increases in brain IL-1beta protein in the adrenalectomized subjects 2 hr after stress, whether basal corticosterone levels had been maintained. Thus elimination of the stress-induced rise in corticosterone unmasked a robust and widespread increase in brain IL-1beta.
据报道,诸如脂多糖(LPS)所提供的外周免疫刺激可增加大脑中白细胞介素-1β(IL-1β)mRNA水平、免疫反应性及生物活性。应激源产生的许多神经和内分泌反应与LPS刺激后产生的反应相同,但应激源对大脑白细胞介素-1β(IL-1β)的影响尚未得到系统研究。一种用于检测IL-1β的酶联免疫吸附测定(ELISA)被用于测量大鼠大脑中IL-1β蛋白的水平。以不可逃避电击(IS;100次1.6毫安的尾部电击,每次5秒)和LPS(1毫克/千克)作为阳性对照,研究应激源暴露后大脑IL-1β的变化情况。IS后,大鼠在即刻、2小时、7小时、24小时或48小时被处死。大脑被解剖为下丘脑、海马体、小脑、后皮质及孤束核区域。LPS使大脑IL-1β广泛增加,但IS未产生此效果。已知肾上腺糖皮质激素可抑制外周和大脑中IL-1β的产生。因此,有可能应激源确实向大脑IL-1β系统提供了刺激输入,但IL-1β蛋白的产生被IS所产生的快速且持续的高水平糖皮质激素所抑制。为验证这一可能性,将大鼠进行肾上腺切除术或假手术,一半肾上腺切除的大鼠接受皮质酮替代以维持基础皮质酮水平。无论基础皮质酮水平是否得到维持,IS应激2小时后,肾上腺切除的大鼠大脑IL-1β蛋白大幅增加。因此,消除应激诱导的皮质酮升高揭示了大脑IL-1β的强烈且广泛的增加。