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Effects of Sleep Fragmentation and Chronic Latent Viral Infection on Behavior and Inflammation in Mice

机译:睡眠破碎和慢性潜伏病毒感染对小鼠行为和炎症的影响

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摘要

Many chronic diseases are associated with both fatigue and disrupted or nonrestorative sleep. In addition, so-called ‘sickness behaviors’ (for example, anorexia, anhedonia, reduced social interaction, fatigue) are common during infectious and inflammatory disease and have been linked to facets of the immune response. To study these relationships, we used murine gammaherpesvirus (MuGHV), a natural pathogen of wild rodents that provides an experimental model for studying the pathophysiology of an Epstein-Barr (EBV)-like γ-herpesvirus infection in mice. We exposed male and female C57BL/6J mice that were either uninfected or latently infected with MuGHV to either sleep fragmentation (SF) or control conditions and measured the effects on behavior and markers of inflammation. Exposure of infected male mice to SF during the normal somnolent (light) phase significantly reduced locomotor activity during the subsequent active phase, despite an intervening 6-h rest period. Infection was associated with significant increases in lung IFNγ and CXC motif ligand (CXCL) 10 in both male and female mice. In both infected and uninfected male mice, exposure to SF was associated with lower levels of IL1β and C-C motif ligand (CCL) 3 in lung. Exposure of infected female mice to SF led to reductions in lung IL2, CXCL1, and CCL 3. Thus, compared with control conditions, SF was generally associated with lower concentrations of various cytokines in lung. These findings, together with our previous work, indicate that complex interactions among several host factors likely contribute to the behavioral and inflammatory changes associated with viral infection and sleep disruption even in a well-controlled mouse model.
机译:许多慢性疾病与疲劳以及睡眠中断或恢复性睡眠有关。此外,在传染性和炎症性疾病中,常见的“疾病行为”(例如厌食症,性欲低下,社交互动减少,疲劳)很常见,并且与免疫反应的各个方面有关。为了研究这些关系,我们使用了鼠γ疱疹病毒(MuGHV),这是一种野生啮齿动物的自然病原体,为研究小鼠爱泼斯坦-巴尔(EBV)样γ疱疹病毒感染的病理生理学提供了实验模型。我们将未感染或潜伏感染了MuGHV的雄性和雌性C57BL / 6J小鼠暴露于睡眠碎片(SF)或对照条件下,并测量了对行为和炎症标志物的影响。尽管有6小时的休息时间,但在正常的睡眠(轻度)阶段将感染的雄性小鼠暴露于SF会显着降低随后的活动阶段的运动能力。感染与雄性和雌性小鼠的肺IFNγ和CXC基序配体(CXCL)10显着增加有关。在感染和未感染的雄性小鼠中,暴露于SF与肺中IL1β和C-C基序配体(CCL)3的较低水平相关。将感染的雌性小鼠暴露于SF会导致肺IL2,CXCL1和CCL 3降低。因此,与对照条件相比,SF通常与肺中各种细胞因子的较低浓度相关。这些发现以及我们以前的工作表明,即使在控制良好的小鼠模型中,几种宿主因素之间的复杂相互作用也可能导致与病毒感染和睡眠破坏相关的行为和炎症变化。

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