Abbasi Asghar, de Paula Vieira Rodolfo, Bischof Felix, Walter Michael, Movassaghi Masoud, Berchtold Nicole C, Niess Andreas M, Cotman Carl W, Northoff Hinnak
Institute for Memory Impairments and Neurological Disorders (MIND Institute), University of California-Irvine (UCI), Irvine, CA, USA.
Institute for Memory Impairments and Neurological Disorders (MIND Institute), Gillespie Neuroscience Research Facility, 1113, University of California, Irvine, 92697.4540, USA.
J Neuroinflammation. 2016 Nov 10;13(1):289. doi: 10.1186/s12974-016-0758-5.
While exercise effects on the immune system have received increasing attention in recent years, it remains unclear to what extent gender and fluctuations in sex hormones during menstrual cycle influence immunological responses to exercise.
We investigated mRNA changes induced through exhaustive exercise (half-marathon; pre-exercise and post-exercise [30 min, 3 h, 24 h] on whole blood cultures ± lipopolysaccharide [LPS] [1 h]) with a specific focus on sex differences (men vs women in luteal phase) as an extension of our previous study.
Inflammation related signaling pathways, TLRs, cytosolic DNA sensing and RIG-I like receptors were differentially activated between sexes in LPS-stimulated cultures. Genes differentially regulated between sexes included TNIP-1, TNIP-3, IL-6, HIVEP1, CXCL3, CCR3, IL-8, and CD69, revealing a bias towards less anti-inflammatory gene regulation in women compared to men. In addition, several genes relevant to brain function (KMO, DDIT4, VEGFA, IGF1R, IGF2R, and FGD4) showed differential activation between sexes. Some of these genes (e.g., KMO in women, DDIT4 in both sexes) potentially constitute neuroprotective mechanisms.
These data reveal that the exercise-induced change in gene expression might be gender and menstrual cycle phase dependent.
近年来,运动对免疫系统的影响受到了越来越多的关注,但性别以及月经周期中性激素波动对运动免疫反应的影响程度仍不清楚。
作为我们之前研究的延伸,我们研究了力竭运动(半程马拉松;运动前及运动后[30分钟、3小时、24小时]对全血培养物±脂多糖[LPS][1小时])诱导的mRNA变化,特别关注性别差异(黄体期的男性与女性)。
在LPS刺激的培养物中,炎症相关信号通路、Toll样受体(TLRs)、胞质DNA感应和视黄酸诱导基因I样受体在两性之间被差异性激活。两性之间差异调节的基因包括TNIP-1、TNIP-3、IL-6、HIVEP1、CXCL3、CCR3、IL-8和CD69,表明与男性相比,女性的抗炎基因调节倾向较弱。此外,一些与脑功能相关的基因(KMO、DDIT4、VEGFA、IGF1R、IGF2R和FGD4)在两性之间表现出差异性激活。其中一些基因(例如女性中的KMO,两性中的DDIT4)可能构成神经保护机制。
这些数据表明,运动诱导的基因表达变化可能依赖于性别和月经周期阶段。