Estébanez Brisamar, de Paz José A, Cuevas María J, González-Gallego Javier
Institute of Biomedicine (IBIOMED), University of León, León, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
Front Physiol. 2018 Dec 5;9:1744. doi: 10.3389/fphys.2018.01744. eCollection 2018.
The endoplasmic reticulum (ER) is a dynamic and multifunctional organelle responsible for protein biosynthesis, folding, assembly and modifications. Loss of protein folding regulation, which leads to unfolded or misfolded proteins accumulation inside the ER lumen, drives ER stress (ERS) and unfolded protein response (UPR) activation. During aging, there is a decline in the ability of the cell to handle protein folding, accumulation and aggregation, and the function of UPR is compromised. There is a progressive failure of the chaperoning systems and a decline in many of its components, so that the UPR activation cannot rescue the ERS. Physical activity has been proposed as a powerful tool against aged-related diseases, which are linked to ERS. Interventional studies have demonstrated that regular exercise is able to decrease oxidative stress and inflammation and reverse mitochondrial and ER dysfunctions. Exercise-induced metabolic stress could activate the UPR since muscle contraction is directly involved in its activation, mediating exercise-induced adaptation responses. In fact, regular moderate-intensity exercise-induced ERS acts as a protective mechanism against current and future stressors. However, biological responses vary according to exercise intensity and therefore induce different degrees of ERS and UPR activation. This article reviews the effects of aging and exercise on ERS and UPR, also analyzing possible changes induced by different types of exercise in elderly subjects.
内质网(ER)是一种动态的多功能细胞器,负责蛋白质的生物合成、折叠、组装和修饰。蛋白质折叠调控的丧失会导致未折叠或错误折叠的蛋白质在内质网腔中积累,从而引发内质网应激(ERS)和未折叠蛋白反应(UPR)的激活。在衰老过程中,细胞处理蛋白质折叠、积累和聚集的能力下降,UPR的功能也受到损害。伴侣系统逐渐失效,其许多组成部分减少,因此UPR的激活无法挽救ERS。体育活动被认为是对抗与衰老相关疾病的有力工具,这些疾病与ERS有关。干预性研究表明,定期锻炼能够降低氧化应激和炎症,并逆转线粒体和内质网功能障碍。运动诱导的代谢应激可以激活UPR,因为肌肉收缩直接参与其激活过程,介导运动诱导的适应性反应。事实上,定期进行中等强度运动诱导的ERS可作为一种针对当前和未来应激源的保护机制。然而,生物学反应会因运动强度而异,因此会诱导不同程度的ERS和UPR激活。本文综述了衰老和运动对ERS和UPR的影响,还分析了不同类型运动对老年受试者可能产生的变化。