Kon Michihiro, Tanimura Yuko
Department of Health Care and Sports, Faculty of Human Life Design, Toyo University, 1-7-11, Akabanedai, Kita-ku, Tokyo 115-0053, Japan.
Department of Sports Research, Japan Institute of Sports Sciences, 3-15-1 Nishigaoka, Kita-ku, Tokyo 115-0056, Japan.
Cytokine. 2023 Jan;161:156083. doi: 10.1016/j.cyto.2022.156083. Epub 2022 Nov 7.
Aerobic exercise is an effective therapeutic strategy to manage metabolic disorders. However, the mechanisms of aerobic exercise-induced improvements in metabolic diseases are not completely understood. Complement C1q/tumor necrosis factor-related protein (CTRP) 1, CTRP3, CTRP5, and CTRP9 have important roles in improving metabolic disorders via the adenosine monophosphate-activated protein kinase signaling pathway. In this study, we investigated the effects of acute aerobic exercise on circulating CTRP1, CTRP3, CTRP5, and CTRP9 levels in human participants. Eight healthy males with an age of 20.4 ± 0.2 years, height 173.1 ± 1.7 cm, body mass 68.0 ± 1.8 kg, body mass index 22.7 ± 0.7 kg/m, and maximal oxygen uptake (VOmax) 51.3 ± 2.5 mL/kg/min performed acute aerobic cycling exercise at 75 % of their VOmax for 30 min (data are mean ± standard error). Blood samples were obtained before; immediately after; and 30, 60, and 120 min after exercising. Serum concentrations of CTRP1, CTRP3, CTRP5, CTRP9, tumor necrosis factor-α (TNF-α), and insulin were measured. The CTRP1 concentration significantly increased immediately after exercising and remained elevated for up to 120 min (p < 0.01). The CTRP3 concentration significantly increased at 60 min after exercise (p < 0.05), and the increasing trend continued until at least 120 min after exercise (p < 0.01). The CTRP5, CTRP9, TNF-α, and insulin concentrations significantly increased immediately after exercise (p < 0.05, p < 0.01, p < 0.05, and p < 0.05, respectively) and decreased thereafter. A significant correlation was observed between the peak post-exercise concentrations of CTRP1 and TNF-α (p < 0.05); however, no correlation was observed between the peak post-exercise concentrations of CTRP3 and insulin. The results of this study indicate that acute aerobic exercise may enhance the secretion of CTRP1, CTRP3, CTRP5, and CTRP9 in healthy adults.
有氧运动是管理代谢紊乱的一种有效治疗策略。然而,有氧运动改善代谢疾病的机制尚未完全明确。补体C1q/肿瘤坏死因子相关蛋白(CTRP)1、CTRP3、CTRP5和CTRP9通过腺苷单磷酸激活蛋白激酶信号通路在改善代谢紊乱方面发挥重要作用。在本研究中,我们调查了急性有氧运动对人类受试者循环中CTRP1、CTRP3、CTRP5和CTRP9水平的影响。八名健康男性,年龄20.4±0.2岁,身高173.1±1.7厘米,体重68.0±1.8千克,体重指数22.7±0.7千克/米,最大摄氧量(VOmax)51.3±2.5毫升/千克/分钟,以其VOmax的75%进行了30分钟的急性有氧自行车运动(数据为平均值±标准误)。在运动前、运动结束后即刻以及运动后30、60和120分钟采集血样。检测血清中CTRP1、CTRP3、CTRP5、CTRP9、肿瘤坏死因子-α(TNF-α)和胰岛素的浓度。CTRP1浓度在运动结束后即刻显著升高,并持续升高至120分钟(p<0.01)。CTRP3浓度在运动后60分钟显著升高(p<0.05),且升高趋势至少持续至运动后120分钟(p<0.01)。CTRP5、CTRP9、TNF-α和胰岛素浓度在运动结束后即刻显著升高(分别为p<0.05、p<0.01、p<0.05和p<0.05),随后下降。运动后CTRP1峰值浓度与TNF-α之间存在显著相关性(p<0.05);然而,运动后CTRP3峰值浓度与胰岛素之间未观察到相关性。本研究结果表明,急性有氧运动可能会增强健康成年人CTRP1、CTRP3、CTRP5和CTRP9的分泌。