Goujon E, Parnet P, Laye S, Combe C, Kelley K W, Dantzer R
INRA-INSERM, Bordeaux, France.
Brain Behav Immun. 1995 Dec;9(4):292-303. doi: 10.1006/brbi.1995.1028.
Mice injected with LPS (10 mu g/mouse, sc) or saline were submitted to a 15-min restraint stress and sacrificed 1 or 2 h later to assess the effect of stress on the induction of interleukin-1beta (IL-1beta) and other proinflammatory cytokines (IL-1alpha, IL-1ra, IL-6, and tumor necrosis factor-alpha) in the spleen, pituitary, hypothalamus, hippocampus, and striatum. LPS-induced cytokine gene expression, as determined by comparative RT-PCR, was lower in stressed than in nonstressed mice. LPS increased plasma and tissue levels of IL-1beta, as determined by ELISA, but this effect was less marked in stressed than in nonstressed mice. These results are discussed in relation to the modulatory effects of glucocorticoids on cytokine production.
给小鼠注射脂多糖(10微克/只,皮下注射)或生理盐水后,对其施加15分钟的束缚应激,1或2小时后处死小鼠,以评估应激对脾脏、垂体、下丘脑、海马体和纹状体中白细胞介素-1β(IL-1β)及其他促炎细胞因子(IL-1α、IL-1ra、IL-6和肿瘤坏死因子-α)诱导的影响。通过比较逆转录聚合酶链反应测定,脂多糖诱导的细胞因子基因表达在应激小鼠中低于非应激小鼠。通过酶联免疫吸附测定法测定,脂多糖增加了血浆和组织中IL-1β的水平,但这种作用在应激小鼠中不如在非应激小鼠中明显。结合糖皮质激素对细胞因子产生的调节作用对这些结果进行了讨论。