Abstract

The loss of skeletal muscle mass and strength is known as sarcopenia; it is characterized as a progressive and generalized muscle disorder associated with aging. This deterioration can seriously compromise the elderly's health and reduce their quality of life. In addition to age, there are other factors that induce muscle mass loss, among which are sedentary lifestyle, chronic diseases, inflammation, and obesity. In recent years, a new clinical condition has been observed in older adults that affects their physical capacities and quality of life, which is known as osteosarcopenic obesity (OSO). Osteoporosis, sarcopenia, and obesity coexist in this condition. Physical exercise and nutritional management are the most widely used interventions for the treatment and prevention of sarcopenia. However, in older adults, physical exercise and protein intake do not have the same outcomes observed in younger people. Here, we used a low-intensity exercise routine for a long period of time (LIERLT) in order to delay the OSO appearance related to sedentarism and aging in female Wistar rats. The LIERLT routine consisted of walking at 15 m/min for 30 min, five days a week for 20 months. To evaluate the effects of the LIERLT routine, body composition was determined using DXA-scan, additionally, biochemical parameters, inflammatory profile, oxidative protein damage, redox state, and serum concentration of GDF-11 at different ages were evaluated (4, 8, 12, 18, 22, and 24 months). Our results show that the LIERLT routine delays OSO phenotype in old 24-month-old rats, in a mechanism involving the decrease in the inflammatory state and oxidative stress. GDF-11 was evaluated as a protein related to muscle repair and regeneration; interestingly, rats that perform the LIERLT increased their GDF-11 levels.

Highlights

  • Aging is a natural and irreversible process that is characterized by the progressive decline of individual’s physiological, biochemical, and structural functions, which makes the organisms more susceptible to acquiring chronic degenerative diseases related to aging, such as diabetes, obesity, osteoporosis, neurodegenerative diseases, and sarcopenia [1]

  • To determine if a low-intensity exercise routine for a long period of time (LIERLT) delays the osteosarcopenic obesity (OSO) phenotype, the body mass index (BMI) and the body composition were determined in the sedentary (SED) and LIERLT groups during a longitudinal study

  • The results showed a significant increase of 8% in BMI in both study groups during 4 and 8 months of age (SED, p = 0:045; LIERLT, p = 0:048)

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Summary

Introduction

Aging is a natural and irreversible process that is characterized by the progressive decline of individual’s physiological, biochemical, and structural functions, which makes the organisms more susceptible to acquiring chronic degenerative diseases related to aging, such as diabetes, obesity, osteoporosis, neurodegenerative diseases, and sarcopenia [1]. A very well-studied phenotype is sarcopenic obesity (OS), where the negative effects of fat on muscle composition and functionality have been determined This topic has been of considerable interest to researchers from different countries, due to its high association with the health conditions of older adults. Two systematic reviews on OS during aging have highlighted the differences in the evaluation methodologies, the ethnic groups, and the gender as important issues that diversify and complicate OS understanding in humans Another problem is the prevalence, since large variations have been reported; it is known that during aging there is a higher OS occurrence in women, due to the accumulation of visceral fat during postmenopause [5,6,7,8]. Since the highest incidence of this disease is in women, we decided to use female rats for our study, in contrast to most animal studies conducted in males

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