School of Behavioral Sciences, The Academic College of Tel Aviv-Yaffo, Tel Aviv, Israel.
Horm Behav. 2011 Feb;59(2):257-64. doi: 10.1016/j.yhbeh.2010.12.002. Epub 2010 Dec 15.
Influenza virus infection is a significant public health problem; however factors affecting the incidence and severity of disease have not been fully elucidated. The present study sought to examine the role of sex and stress in mediating susceptibility to an influenza viral infection in mice. Male and female mice underwent repeated cycles of restraint (RST) stress, followed by an influenza A/PR8 virus infection. Following these manipulations, levels of circulating corticosterone, lung proinflammatory cytokine gene expression and sickness behavior were examined. The data indicate sex differences in several aspects of the response to the A/PR8 virus infection. The kinetics of lung interleukin-1β mRNA expression were faster in infected males compared to females, while circulating corticosterone levels were elevated in infected females, but not in males. Anorexia and reduced saccharin consumption began earlier and symptoms were more pronounced in infected males than in females. In addition, RST modulated the response to the A/PR8 virus infection. Proinflammatory cytokine gene expression in response to infection was enhanced and sickness behavior was modulated by RST in both males and females. These data suggest that males mount more vigorous immune and behavioral responses to influenza viral infection compared to females, and stress exacerbates the response in both males and females. In conclusion, complex interactions between biological and behavioral factors are involved in mediating individual differences in health and disease. Additional studies may help uncover some of the factors contributing to the individual differences in susceptibility to influenza infection.
流感病毒感染是一个重大的公共卫生问题;然而,影响疾病发病率和严重程度的因素尚未得到充分阐明。本研究旨在探讨性别和应激在介导小鼠流感病毒感染易感性中的作用。雄性和雌性小鼠接受了反复的束缚(RST)应激,然后感染甲型流感病毒/PR8。进行这些操作后,检测了循环皮质酮水平、肺部促炎细胞因子基因表达和疾病行为。数据表明,性别在对 A/PR8 病毒感染的反应的几个方面存在差异。感染雄性小鼠肺部白细胞介素-1β mRNA 表达的动力学比雌性更快,而感染雌性小鼠的循环皮质酮水平升高,但感染雄性小鼠的皮质酮水平没有升高。感染雄性小鼠的厌食和蔗糖消耗减少开始更早,症状比感染雌性小鼠更明显。此外,RST 调节了对 A/PR8 病毒感染的反应。感染后促炎细胞因子基因表达增强,应激在雄性和雌性中均调节疾病行为。这些数据表明,与雌性相比,雄性对流感病毒感染产生更强烈的免疫和行为反应,应激在雄性和雌性中均加重了这种反应。总之,生物和行为因素之间的复杂相互作用参与介导个体在健康和疾病方面的差异。进一步的研究可能有助于揭示导致个体对流感感染易感性差异的一些因素。