Zager A, Andersen M L, Ruiz F S, Antunes I B, Tufik S
Department of Psychobiology, Universidade Federal de São Paulo, Rua Napoleão de Barros 925, Vila Clementino 04024-002, São Paulo, SP, Brazil.
Am J Physiol Regul Integr Comp Physiol. 2007 Jul;293(1):R504-9. doi: 10.1152/ajpregu.00105.2007. Epub 2007 Apr 4.
Sleep deprivation is now recognized as an increasingly common condition inherent to modern society, and one that in many ways, is detrimental to certain physiological systems, namely, immune function. Although sleep is now viewed by a significant body of researchers as being essential for the proper working of a host of defense systems, the consequences of a lack of sleep on immune function remains to be fully comprehended. The aim of the current study was to investigate how paradoxical sleep deprivation (PSD) for 24 and 96 h and sleep restriction (SR) for 21 days by the modified multiple-platform method, and their respective 24-h recovery periods, affect immune activation in rats. To this end, we assessed circulating white blood cell counts, lymphocyte count within immune organs, as well as Ig and complement production. The data revealed that PSD for 96 h increased complement C3 and corticosterone concentration in relation to the control group. In contrast, the spleen weight, total leukocytes, and lymphocytes decreased during SR for 21 days when compared with the control group, although production of a certain class of immunoglobulin, the IgM, did increase. After recovery sleep, lymphocyte count in axillary lymph nodes grew when rats had rebound sleep after PSD for 24 h, neutrophils increased after PSD 96 h and lymphocytes numbers were higher after SR 21 days. Such alterations during sleep deprivation suggest only minor alterations of nonspecific immune parameters during acute PSD, and a significant impairment in cellular response during chronic SR.
睡眠剥夺如今被认为是现代社会中日益普遍的一种现象,而且在很多方面,它对某些生理系统,即免疫功能,是有害的。尽管现在有大量研究人员认为睡眠对于许多防御系统的正常运作至关重要,但睡眠不足对免疫功能的影响仍有待充分理解。本研究的目的是通过改良的多平台方法,研究24小时和96小时的异相睡眠剥夺(PSD)以及21天的睡眠限制(SR),及其各自24小时的恢复期,如何影响大鼠的免疫激活。为此,我们评估了循环白细胞计数、免疫器官内的淋巴细胞计数以及免疫球蛋白和补体的产生。数据显示,与对照组相比,96小时的PSD会增加补体C3和皮质酮浓度。相反,与对照组相比,21天的SR期间脾脏重量、总白细胞和淋巴细胞减少,尽管某一类免疫球蛋白IgM的产生确实增加了。恢复睡眠后,24小时PSD后出现反弹睡眠的大鼠腋窝淋巴结中的淋巴细胞计数增加,96小时PSD后中性粒细胞增加,21天SR后淋巴细胞数量更高。睡眠剥夺期间的这些变化表明,急性PSD期间非特异性免疫参数仅有轻微变化,而慢性SR期间细胞反应有显著受损。