Abstract

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.

Highlights

  • The endoplasmic reticulum (ER) plays an essential role in controlling various intracellular physiological functions, including protein translocation, protein folding, calcium homeostasis, and lipid biosynthesis (Naidoo, 2009a)

  • In a study based in 3-weeks voluntary running with mice fed low-fat diet (LFD) or high fat diet (HFD), eukaryotic translation initiation factor 2 subunit α (eIF2α) mRNA expression was upregulated in brain and liver of high runners with both LFD and HFD, while eIF2α phosphorylated (peIF2α) only increased in hippocampus of HFDhigh runners (Kim et al, 2010)

  • Most of these conflicting findings may be due to differences in factors such as the use of young, adult or aged animal models, as well as the animal species used or their health status, the tissues analyzed or the acute and chronic training protocols carried out

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Summary

INTRODUCTION

The endoplasmic reticulum (ER) plays an essential role in controlling various intracellular physiological functions, including protein translocation, protein folding, calcium homeostasis, and lipid biosynthesis (Naidoo, 2009a). Physiological conditions increase the protein folding demand, which may trigger loss of its regulation and leads to unfolded or misfolded proteins accumulation inside the ER lumen (Pereira et al, 2016). This accumulation drives ER stress (ERS) and unfolded protein response (UPR) activation. There is a decline in cell capacity to handle protein folding, accumulation, and aggregation, which may be, in part, due to a progressive failure of the chaperoning systems It seems that UPR activation cannot rescue the ERS, since some researches show a decline in many of UPR components (Naidoo, 2009b). The aims of this review are to briefly identify the main effects of both aging and exercise on the ERS and UPR, and to analyze changes on ERS and UPR following the performance of different types of exercise by elderly subjects

UPR ACTIVATION
UPR IN AGING
EXERCISE AND UPR
UPR IN EXERCISE AND AGING
EFFECTS OF EXERCISE ON UPR IN AGING
CONCLUSIONS
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