Chen Hui, Ma Xuan, Cao Lixing, Zhao Shuang, Zhao Chong, Yin Shutao, Hu Hongbo
Department of Food Nutrition and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China.
Foods. 2021 Dec 16;10(12):3120. doi: 10.3390/foods10123120.
Multiple mechanisms are involved in exercise-induced fatigue, including energy depletion, metabolite accumulation, and oxidative stress, etc. The mechanistic findings provide a rationale for a multi-targeted approach to exercise-induced fatigue management. This study created a multi-ingredient formula mixed with valine, isoleucine, leucine, β-alanine, creatine, l-carnitine, quercetin, and betaine, based on the functional characteristics of these agents, and evaluated the preventive effect of this mechanism-based formula on exercise-induced fatigue. Results showed that the 7-d formula supplement significantly increased the running duration time of mice by 14% and the distance by 20% in an exhaustive treadmill test, indicating that the formula could delay fatigue appearance and improve exercise performance. Mechanistically, the formula enhanced fatty acid oxidation and spared liver glycogen by regulating the fat/glucose metabolism-related signaling pathways, including phospho-adenosine monophosphate-activated protein kinase α (p-AMPKα), phospho-acetyl CoA carboxylase (p-ACC), carnitine palmitoyl-transferase 1B (CPT1B), fatty acid translocase (CD36), and glucose transporter type 4 (GLUT4), and increased antioxidant capacity. The findings suggested that the formula tested in this study effectively ameliorated exercise-induced fatigue by targeting multi-signaling pathways, showing promise as a regimen to fight exercise-induced fatigue.
运动诱导的疲劳涉及多种机制,包括能量消耗、代谢产物积累和氧化应激等。这些机制研究结果为运动诱导疲劳管理的多靶点方法提供了理论依据。本研究根据缬氨酸、异亮氨酸、亮氨酸、β-丙氨酸、肌酸、左旋肉碱、槲皮素和甜菜碱等物质的功能特性,创建了一种多成分配方,并评估了这种基于机制的配方对运动诱导疲劳的预防作用。结果表明,在力竭性跑步机测试中,为期7天的配方补充剂显著使小鼠的跑步持续时间增加了14%,跑步距离增加了20%,表明该配方可以延迟疲劳出现并提高运动表现。从机制上讲,该配方通过调节脂肪/葡萄糖代谢相关信号通路,包括磷酸化腺苷单磷酸激活蛋白激酶α(p-AMPKα)、磷酸化乙酰辅酶A羧化酶(p-ACC)、肉碱棕榈酰转移酶1B(CPT1B)、脂肪酸转运蛋白(CD36)和葡萄糖转运蛋白4(GLUT4),增强脂肪酸氧化并节省肝糖原,并提高抗氧化能力。研究结果表明,本研究中测试的配方通过靶向多信号通路有效改善了运动诱导的疲劳,有望成为对抗运动诱导疲劳的一种方案。