Department of Biobehavioral Health, The Pennsylvania State University, United States.
Department of Biobehavioral Health, The Pennsylvania State University, United States; College of Nursing, The Pennsylvania State University, United States.
Psychoneuroendocrinology. 2020 Nov;121:104863. doi: 10.1016/j.psyneuen.2020.104863. Epub 2020 Sep 10.
Empirical and theoretical evidence suggest that because of the co-evolution of the endocrine and immune response systems, different types of stressors may lead to similar levels of physiological activation. The present analyses examined associations between two physiological stress responses: the cortisol response to an acute laboratory stressor and ex vivo lipopolysaccharide (LPS) stimulated inflammatory cytokine production.
Healthy middle-aged adults (N = 65) completed testing at two appointments, two weeks apart. Blood was collected at each appointment to measure circulating inflammatory cytokine levels and stimulated inflammatory cytokine production after 4 and 24 hours of incubation with LPS. A cumulative standardized composite measure of inflammation was calculated using the cytokines interleukin-6 (IL-6), interleukin-1β (IL-1β), and interferon-γ (IFN-γ). At visit two, after the blood draw, participants completed the Trier Social Stress Test (TSST); saliva samples were collected before and after to generate cortisol response curves (area under the curve with respect to ground [AUC] and increase/decrease [AUC]).
AUC was significantly associated with stimulated cytokine production at visit 2 after both 4 hours (B = 6.89; p = 0.007) and 24 hours (B = 7.50; p = 0.005) of incubation, controlling for age, sex, and BMI. AUC was also significantly associated with stimulated cytokine production at visit 2 after 4 hours (B = 6.28; p = 0.004) and 24 hours (B = 6.16; p = 0.007) of incubation, controlling for age, sex, and BMI. Stimulated inflammatory cytokine production was strongly correlated across the two visits (2 weeks apart) after 4 hours of incubation (r = 0.80, p < 0.001) and after 24 hours (r = 0.80, p < 0.001). Within each visit, stimulated cytokine production after 4 hours was significantly correlated with stimulated inflammation at 24 hours (r = 0.93-0.94, p < 0.05) CONCLUSIONS: These results suggest that LPS-stimulated inflammatory cytokine production and the cortisol response to the TSST contain comparable information about acute human physiological stress responses. Moreover, measurement of stimulated cytokines was highly stable across a two-week time period whether measured after 4 or 24 hours of incubation with LPS.
实证和理论证据表明,由于内分泌和免疫反应系统的共同进化,不同类型的应激源可能导致相似水平的生理激活。本分析研究了两种生理应激反应之间的关联:皮质醇对急性实验室应激源的反应和体外脂多糖(LPS)刺激的炎性细胞因子产生。
健康中年成年人(N=65)在两周内分两次完成测试。在每次就诊时采集血液,以测量循环炎性细胞因子水平,并在 LPS 孵育 4 和 24 小时后测量刺激的炎性细胞因子产生。使用细胞因子白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和干扰素-γ(IFN-γ)计算炎症的累积标准化综合测量值。在第二次就诊时,在采血后,参与者完成了特里尔社会应激测试(TSST);采集唾液样本以生成皮质醇反应曲线(与地面的曲线下面积[AUC]和增加/减少[AUC])。
AUC 与 4 小时(B=6.89;p=0.007)和 24 小时(B=7.50;p=0.005)孵育后 2 次就诊时刺激的细胞因子产生显著相关,控制年龄、性别和 BMI。AUC 与 4 小时(B=6.28;p=0.004)和 24 小时(B=6.16;p=0.007)孵育后 2 次就诊时刺激的细胞因子产生也显著相关,控制年龄、性别和 BMI。4 小时孵育后两次就诊时的刺激细胞因子产生具有很强的相关性(r=0.80,p<0.001)和 24 小时(r=0.80,p<0.001)。在每次就诊中,4 小时刺激细胞因子产生与 24 小时刺激炎症显著相关(r=0.93-0.94,p<0.05)。
这些结果表明,LPS 刺激的炎性细胞因子产生和 TSST 对皮质醇的反应包含关于急性人体生理应激反应的可比信息。此外,无论在 LPS 孵育 4 小时还是 24 小时后测量,刺激细胞因子的测量在两周的时间内具有高度稳定性。