School of Kinesiology, Louisiana State University, Huey P Long Fieldhouse, Baton Rouge, Louisina, USA.
Pennington Biomedical Research Center, Baton Rouge, Louisina, USA.
Physiol Rep. 2021 Dec;9(23):e15147. doi: 10.14814/phy2.15147.
Regular exercise is associated with changes in peripheral blood mononuclear cell (PBMC) proportions that have enhanced effector functions in young and old adults; however, the effects of acute exercise on PBMC nutrient sensors and metabolic function in active young adults is unknown. To fill this gap, activation status and nutrient-sensing mechanisms of PBMCs isolated from 21 healthy active adults (20-35 yr; 36.5 ± 6.3 V̇O ) were characterized before and after 30 min of moderate-to-vigorous cycling (65%-75% V̇O ). In addition, changes in PBMC mitochondrial respiratory function in response to exercise were assessed using high-resolution respirometry. There was an increase in the number of activated CD69+/CD4 (79% increase) and CD69+/CD8 (166% increase) T-cells in response to the acute bout of exercise, while the nutrient-sensing mechanisms remained unchanged. PBMC mitochondrial respiration did not increase on a cell-per-cell basis, however, mitochondrial oxidative capacity (OXPHOS) increased at the tissue level (18.6 pmol/(sml blood) versus 29.3 pmol/(sml blood); p < 0.05) in response to acute exercise. Thus, this study shows that acute exercise preferentially mobilizes activated T-cells while concomitantly increasing PBMC mitochondrial oxidative capacity at the tissue level, rather than acutely changing mitochondrial oxidative capacity at the cellular level in young adults.
定期运动与外周血单核细胞(PBMC)比例的变化有关,这些变化增强了年轻和老年成年人的效应功能;然而,急性运动对活跃的年轻成年人 PBMC 营养传感器和代谢功能的影响尚不清楚。为了填补这一空白,本研究在 21 名健康活跃的成年人(20-35 岁;36.5±6.3 VO )中,在进行 30 分钟的中等至剧烈强度骑行(65%-75% VO )前后,对 PBMC 的激活状态和营养感应机制进行了特征分析。此外,还使用高分辨率呼吸测定法评估了 PBMC 线粒体呼吸功能对运动的反应变化。急性运动后,CD69+/CD4(增加 79%)和 CD69+/CD8(增加 166%)T 细胞的数量增加,而营养感应机制保持不变。虽然 PBMC 线粒体呼吸在细胞水平上没有增加,但线粒体氧化能力(OXPHOS)在组织水平上增加(从 18.6 pmol/(sml 血液)增加到 29.3 pmol/(sml 血液);p<0.05)。因此,本研究表明,急性运动优先动员活化的 T 细胞,同时增加组织水平的 PBMC 线粒体氧化能力,而不是在年轻成年人中急性改变细胞水平的线粒体氧化能力。