Brinkmann C, Bizjak D A, Bischof S, Latsch J, Brixius K, Bloch W, Grau M
Department of Molecular and Cellular Sport Medicine, Institute of Cardiovascular Research and Sport Medicine, German Sport University Cologne, Germany.
Department of Preventive and Rehabilitative Sport Medicine, Institute of Cardiovascular Research and Sport Medicine, German Sport University Cologne, Germany.
Clin Hemorheol Microcirc. 2016 Sep 12;63(3):173-84. doi: 10.3233/CH-151957.
This study examines the effects of endurance training on red blood cells (RBC) in seventeen non-insulin-dependent type 2 diabetic men with a special focus on in vivo RBC aging. Venous blood was collected pre- and post-training at rest. RBC from whole blood and RBC separated according to cell age by density-gradient centrifugation were analyzed. RBC deformability was measured by ektacytometry. Immunohistochemical staining was performed to quantify the RBC-nitric oxide (NO) synthase activation (RBC-NOSSer1177) because RBC-NOS-produced NO can contribute to increased RBC deformability. The proportion of "young" RBC was significantly higher post-training. RBC deformability of all RBC (RBC of all ages) remained unaltered post-training. During RBC aging, RBC deformability decreased in both pre- and post-training. However, the training significantly increased RBC deformability in "young" and reduced their deformability in aging RBC. RBC-NOS activation remained unaltered in all RBC post-training. It tendentially increased in aging RBC pre-training, but did not change during aging post-training. The training significantly reduced RBC-NOS activation in "old" RBC. Endurance training may improve the RBC system (higher amount of "young" RBC which are more deformable). It remains speculative whether changes in older RBC (reduced RBC-NOS activation and deformability) could lead to more rapid elimination of aged RBC.
本研究调查了耐力训练对17名非胰岛素依赖型2型糖尿病男性红细胞(RBC)的影响,特别关注体内红细胞衰老情况。在训练前后静息状态下采集静脉血。对全血中的红细胞以及通过密度梯度离心按细胞年龄分离的红细胞进行分析。通过激光衍射法测量红细胞变形性。进行免疫组织化学染色以量化红细胞一氧化氮(NO)合酶激活情况(RBC-NOSSer1177),因为红细胞一氧化氮合酶产生的NO有助于提高红细胞变形性。训练后“年轻”红细胞的比例显著更高。所有红细胞(各年龄段红细胞)的变形性在训练后保持不变。在红细胞衰老过程中,训练前和训练后的红细胞变形性均降低。然而,训练显著提高了“年轻”红细胞的变形性,并降低了衰老红细胞的变形性。训练后所有红细胞中的红细胞一氧化氮合酶激活情况保持不变。训练前衰老红细胞中的该激活情况有增加趋势,但训练后衰老过程中未发生变化。训练显著降低了“老”红细胞中的红细胞一氧化氮合酶激活情况。耐力训练可能会改善红细胞系统(“年轻”红细胞数量增加且更具变形性)。衰老红细胞的变化(红细胞一氧化氮合酶激活和变形性降低)是否会导致衰老红细胞更快清除仍有待推测。