Department of Biology, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico.
Department of Biology, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico ; Metabolomics Research Center, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico.
PLoS One. 2013 Dec 11;8(12):e81459. doi: 10.1371/journal.pone.0081459. eCollection 2013.
Combinatorial therapies using voluntary exercise and diet supplementation with polyunsaturated fatty acids have synergistic effects benefiting brain function and behavior. Here, we assessed the effects of voluntary exercise on anxiety-like behavior and on total FA accumulation within three brain regions: cortex, hippocampus, and cerebellum of running versus sedentary young adult male C57/BL6J mice. The running group was subjected to one month of voluntary exercise in their home cages, while the sedentary group was kept in their home cages without access to a running wheel. Elevated plus maze (EPM), several behavioral postures and two risk assessment behaviors (RABs) were then measured in both animal groups followed immediately by blood samplings for assessment of corticosterone levels. Brains were then dissected for non-targeted lipidomic analysis of selected brain regions using gas chromatography coupled to mass spectrometry (GC/MS). Results showed that mice in the running group, when examined in the EPM, displayed significantly lower anxiety-like behavior, higher exploratory and risky behaviors, compared to sedentary mice. Notably, we found no differences in blood corticosterone levels between the two groups, suggesting that the different EPM and RAB behaviors were not related to reduced physiological stress in the running mice. Lipidomics analysis revealed a region-specific cortical decrease of the saturated FA: palmitate (C16:0) and a concomitant increase of polyunsaturated FA, arachidonic acid (AA, omega 6-C20: 4) and docosahexaenoic acid (DHA, omega 3-C22: 6), in running mice compared to sedentary controls. Finally, we found that running mice, as opposed to sedentary animals, showed significantly enhanced cortical expression of phospholipase A2 (PLA2) protein, a signaling molecule required in the production of both AA and DHA. In summary, our data support the anxiolytic effects of exercise and provide insights into the molecular processes modulated by exercise that may lead to its beneficial effects on mood.
组合疗法结合了自愿运动和富含多不饱和脂肪酸的饮食补充,具有协同作用,有益于大脑功能和行为。在这里,我们评估了自愿运动对焦虑样行为以及三个大脑区域(皮层、海马体和小脑)中总 FA 积累的影响:跑步组和久坐组的年轻成年雄性 C57/BL6J 小鼠。跑步组在其笼中进行了一个月的自愿运动,而久坐组则被关在其笼中,无法使用跑步轮。然后在两组动物中测量了高架十字迷宫(EPM)、几种行为姿势和两种风险评估行为(RAB),然后立即进行血液取样以评估皮质酮水平。然后将大脑解剖用于使用气相色谱法与质谱法(GC/MS)对选定脑区进行非靶向脂质组学分析。结果表明,在 EPM 中检查时,跑步组的小鼠表现出明显较低的焦虑样行为、更高的探索性和冒险行为,与久坐组的小鼠相比。值得注意的是,我们发现两组之间的血液皮质酮水平没有差异,这表明跑步小鼠的不同 EPM 和 RAB 行为与降低的生理应激无关。脂质组学分析显示,与久坐对照组相比,跑步小鼠皮质中饱和脂肪酸:棕榈酸(C16:0)减少,多不饱和脂肪酸、花生四烯酸(AA,ω 6-C20: 4)和二十二碳六烯酸(DHA,ω 3-C22: 6)增加。最后,我们发现与久坐动物相比,跑步小鼠表现出明显增强的皮质磷脂酶 A2(PLA2)蛋白表达,这是一种产生 AA 和 DHA 所必需的信号分子。总之,我们的数据支持运动的抗焦虑作用,并提供了有关运动调节的分子过程的见解,这些过程可能导致其对情绪的有益影响。