Nieman David C, Zwetsloot Kevin A, Lomiwes Dominic D, Meaney Mary P, Hurst Roger D
Appalachian State University, North Carolina Research Campus Kannapolis, NC, USA.
The New Zealand Institute for Plant and Food Research Ltd. Palmerston North, New Zealand.
Front Physiol. 2016 Sep 27;7:431. doi: 10.3389/fphys.2016.00431. eCollection 2016.
The cytokine response to heavy exertion varies widely for unknown reasons, and this study evaluated the relative importance of glycogen depletion, muscle damage, and stress hormone changes on blood and muscle cytokine measures. Cyclists ( = 20) participated in a 75-km cycling time trial (168 ± 26.0 min), with blood and vastus lateralis muscle samples collected before and after. Muscle glycogen decreased 77.2 ± 17.4%, muscle IL-6, IL-8, and MCP-1 mRNA increased 18.5 ± 2.8-, 45.3 ± 7.8-, and 8.25 ± 1.75-fold, and muscle IL-6, IL-8, and MCP-1 protein increased 70.5 ± 14.1%, 347 ± 68.1%, and 148 ± 21.3%, respectively (all, < 0.001). Serum myoglobin and cortisol increased 32.1 ± 3.3 to 242 ± 48.3 mg/mL, and 295 ± 27.6 to 784 ± 63.5 nmol/L, respectively (both < 0.001). Plasma IL-6, IL-8, and MCP-1 increased 0.42 ± 0.07 to 18.5 ± 3.8, 4.07 ± 0.37 to 17.0 ± 1.8, and 96.5 ± 3.7 to 240 ± 21.6 pg/mL, respectively (all < 0.001). Increases in muscle IL-6, IL-8, and MCP-1 mRNA were unrelated to any of the outcome measures. Muscle glycogen depletion was related to change in plasma IL-6 ( = 0.462, = 0.040), with change in myoglobin related to plasma IL-8 ( = 0.582, = 0.007) and plasma MCP-1 ( = 0.457, = 0.043), and muscle MCP-1 protein ( = 0.588, = 0.017); cortisol was related to plasma IL-8 ( = 0.613, = 0.004), muscle IL-8 protein ( = 0.681, = 0.004), and plasma MCP-1 ( = 0.442, = 0.050). In summary, this study showed that muscle IL-6, IL-8, and MCP-1 mRNA expression after 75-km cycling was unrelated to glycogen depletion and muscle damage, with change in muscle glycogen related to plasma IL-6, and changes in serum myoglobin and cortisol related to the chemotactic cytokines IL-8 and MCP-1.
由于未知原因,细胞因子对剧烈运动的反应差异很大,本研究评估了糖原消耗、肌肉损伤和应激激素变化对血液和肌肉细胞因子指标的相对重要性。20名自行车运动员参加了一场75公里的自行车计时赛(168±26.0分钟),在比赛前后采集血液和股外侧肌样本。肌肉糖原减少了77.2±17.4%,肌肉白细胞介素-6(IL-6)、白细胞介素-8(IL-8)和单核细胞趋化蛋白-1(MCP-1)的信使核糖核酸(mRNA)分别增加了18.5±2.8倍、45.3±7.8倍和8.25±1.75倍,肌肉IL-6、IL-8和MCP-1蛋白分别增加了70.5±14.1%、347±68.1%和148±21.3%(均P<0.001)。血清肌红蛋白和皮质醇分别从32.1±3.3毫克/毫升增加到242±48.3毫克/毫升,以及从295±27.6纳摩尔/升增加到784±63.5纳摩尔/升(均P<0.001)。血浆IL-6、IL-8和MCP-1分别从0.42±0.07皮克/毫升增加到18.5±3.8皮克/毫升、从4.07±0.37皮克/毫升增加到17.0±1.8皮克/毫升、从96.5±3.7皮克/毫升增加到2 /span>40±21.6皮克/毫升(均P<0.001)。肌肉IL-6、IL-8和MCP-1的mRNA增加与任何一项结果指标均无关联。肌肉糖原消耗与血浆IL-6的变化相关(r = 0.462,P = 0.040),肌红蛋白的变化与血浆IL-8(r = 0.582,P = 0.007)和血浆MCP-1(r = 0.457,P = 0.043)以及肌肉MCP-1蛋白相关(r = 0.588,P = 0.017);皮质醇与血浆IL-8(r = 0.613,P = 0.004)、肌肉IL-8蛋白(r = 0.681,P = 0.004)和血浆MCP-1相关(r = 0.442,P = 0.050)。总之,本研究表明,75公里骑行后肌肉IL-6、IL-8和MCP-1的mRNA表达与糖原消耗和肌肉损伤无关,肌肉糖原的变化与血浆IL-6相关,血清肌红蛋白和皮质醇的变化与趋化细胞因子IL-8和MCP-1相关。