Graduate School of Sport Sciences, Waseda University, Tokorozawa, Saitama 359-1192, Japan.
Faculty of Sport Sciences, Waseda University, Tokorozawa, Saitama 359-1192, Japan.
Exerc Immunol Rev. 2024;30:49-62.
Moderate exercise is effective for maintaining or improving overall health. However, excessive exercise that exhausts the adaptive reserve of the body or its ability to positively respond to training stimuli can induce tissue damage and dysfunction of multiple organs and systems. Tissue injury, inflammation, and oxidative stress are reportedly induced in the skeletal muscles, liver, and kidneys after exercise. However, the precise mechanisms underlying acute tissue injury after intense exercise have not yet been fully elucidated. Studies using various experimental models of acute tissue injury, other than intense exercise, have demonstrated infiltration of inflammatory cells, including neutrophils and macrophages. These cells infiltrate injured tissues and induce inflammatory and oxidative stress responses by producing inflammatory cytokines and reactive oxygen species, thereby exacerbating tissue injury. In addition to the activation of blood neutrophils and increase in their levels during and/or after prolonged or intense exercise, chemokines that contribute to leukocyte migration are released, facilitating the migration of neutrophils and monocytes into tissues. Therefore, neutrophils and macrophages, activated by exhaustive exercise, may infiltrate tissues and contribute to exhaustive exercise-induced tissue injury. Recently, the contributions of neutrophils and macrophages to various tissue injuries caused by exhaustive exercise have been reported. In this review, we summarize the involvement of neutrophils and monocytes/macrophages in exhaustive exercise-induced non-skeletal muscle tissue injury. In addition, we present novel data demonstrating the contribution of neutrophils and macrophages to exhaustive exercise-induced cardiac and pulmonary injuries. Our study findings and the evidence presented in this review suggest that neutrophils and macrophages may play pivotal roles in exhaustive exercise-induced tissue injuries.
适度运动有益于维持或改善整体健康。然而,过度的运动可能会耗尽身体的适应储备或其对训练刺激做出积极反应的能力,从而导致组织损伤和多个器官和系统的功能障碍。据报道,运动后骨骼肌、肝脏和肾脏会发生组织损伤、炎症和氧化应激。然而,高强度运动后急性组织损伤的确切机制尚未完全阐明。使用除高强度运动以外的各种急性组织损伤实验模型的研究表明,炎症细胞(包括中性粒细胞和巨噬细胞)会浸润受伤组织。这些细胞通过产生炎症细胞因子和活性氧,诱导炎症和氧化应激反应,从而加重组织损伤。除了在延长或高强度运动期间和/或之后血液中性粒细胞的激活和水平增加外,还会释放有助于白细胞迁移的趋化因子,促进中性粒细胞和单核细胞向组织迁移。因此,在剧烈运动的作用下被激活的中性粒细胞和巨噬细胞可能会浸润组织并导致剧烈运动引起的组织损伤。最近,有研究报道了中性粒细胞和巨噬细胞在剧烈运动引起的各种组织损伤中的作用。在这篇综述中,我们总结了中性粒细胞和单核细胞/巨噬细胞在剧烈运动引起的非骨骼肌组织损伤中的作用。此外,我们还提供了新的数据,证明了中性粒细胞和巨噬细胞在剧烈运动引起的心脏和肺部损伤中的作用。我们的研究结果和本综述中提供的证据表明,中性粒细胞和巨噬细胞可能在剧烈运动引起的组织损伤中发挥关键作用。