- Open Access
The effects of long-term endurance training on the immune and endocrine systems of elderly men: the role of cytokines and anabolic hormones
© Arai et al; licensee BioMed Central Ltd. 2006
- Received: 23 May 2006
- Accepted: 25 August 2006
- Published: 25 August 2006
a decline in immune and endocrine function occurs with aging. The main purpose of this study was to investigate the impact of long-term endurance training on the immune and endocrine system of elderly men. The possible interaction between these systems was also analysed.
elderly runners showed a significantly higher T cell proliferative response and IL-2 production than sedentary elderly controls. IL-2 production was similar to that in young adults. Their serum IL-6 levels were significantly lower than their sedentary peers. They also showed significantly lower IL-3 production in comparison to sedentary elderly subjects but similar to the youngs. Anabolic hormone levels did not differ between elderly groups and no clear correlation was found between hormones and cytokine levels.
highly conditioned elderly men seem to have relatively better preserved immune system than the sedentary elderly men. Long-term endurance training has the potential to decelerate the age-related decline in immune function but not the deterioration in endocrine function.
- Regular Physical Activity
- Anabolic Hormone
- Serum Hormone Level
- Elderly Runner
- SENIEUR Protocol
Human immune function undergoes adverse changes with aging, potentially leading to an increased risk of infections, a greater occurrence of autoantibodies and lymphoproliferative disorders, and a greater morbidity and mortality in the elderly . Of the various components of the immune system, T cells are the most sensitive to the effects of aging . Mitogen-induced T cell proliferation is usually reduced, and this may be the result from disruption of the well-balanced network of regulatory cytokines. The interleukin-2 (IL-2) production tends to diminish with age .
The endocrine system also suffers from senescence . Substantial decline occurs in the hormone levels of at least three endocrine axes: hypothalamic-pituitary-gonadal, hypothalamic-pituitary-adrenal (HPA) and growth hormone-insulin-like growth factor I. Among them, the HPA axis is the one that best integrates the neuroendocrine and immune systems. The relationship between dehydroepiandrosterone sulphate (DHEAS) and interleukin-6 is described. There have been few reports concerning this field in the elderly 
The question arises whether regular physical activity can correct the deleterious effects of aging on the human immune and endocrine systems. There is growing evidence that long-term conditioning may be associated with improved immune functioning in the elderly , and physical activity has been reported to affect the endocrine profile in aged men [7, 8]. No previous studies have examined the impact of long-term training on the immune and endocrine system concomitantly.
The purpose of the present investigation was to examine the effects of long-term endurance training on the T cell proliferative response, broad cytokine profile and serum hormone levels in elderly men and to correlate the anabolic hormones with cytokines.
Preservation of immunological functions is keenly needed to avoid disease and consequently for the improvement of quality of life in the elderly. Several methods to improve the immune system have been tested but their effectiveness is generally controversial . Among them, regular physical exercise has been tested in limited studies and has been proposed as an effective intervention in the aged .
Very little is known about the effect of exercise training on the cytokine profile of elderly humans. Shinkai et al.  showed greater production of IL-2, interferon (IFN)-γ and IL-4 in elderly runners when compared to sedentary peers. Nevertheless, twelve week of resistance strength training did not induce changes in IL-1β, tumor necrosis factor (TNF)-α, IL-2 or IL-6 production in elderly subjects . Jankord and Jemiolo showed lower levels of serum IL-6 and higher levels of serum IL-10 in the very active group compared with the less active group .
Levels of cytokines (pg/ml) in serum of elderly subjects (mean ± S.E.M.)
90.1 ± 3.4
101.9 ± 5.7
3.8 ± 1.9
15.2 ± 4.7*
3.4 ± 3.4
0.6 ± 0.3
3.7 ± 0.9**
0.06 ± 0.04
1.73 ± 0.69
11.5 ± 1.5
20.5 ± 2.5**
In our study, IL-4 and IL-10 (group effect: p = 0.149 and p = 0.934 respectively) were not altered in elderly runners compared to the sedentary group (Figure 2c,d). It is possible that long-term aerobic training does not affect the Th2-like cytokine response in aged men.
In spite of a higher proliferative response and IL-2 production in relation to their sedentary counterparts, the elderly runners did not show any difference in IL-12 production (group effect: p =< 0.001) (Figure 2e). Chronic exercise seem to change T cells function but its effects on monocytes, macrophages and dendritic cells that secrete IL-12 are little known . As a non-specific mitogen phytohemagglutinin-A (PHA) was used to stimulate these cells, future comparison of IL-12 productions induced with specific antigen (bacterial lipopolysaccharide) and of kinetics of release of this cytokine with both stimuli could be done. Since IL-12 is an inducer of Th1 cell generation and upregulates IFN-γ production , the measurement of this cytokine could be also helpful to elucidate this finding.
The effects of exercise training on IL-3 production in elderly people have not been previously investigated. This interleukin is preferentially produced by T cells and it functions as a link between the immune and hemopoietic systems, stimulating the generation and the function of blood cells, specially the pluripotential hemopoietic stem cell and its derivatives . Our active elderly subjects showed lower production and serum levels of IL-3 than their sedentary peers and similar production in relation to young subjects (group effect: p =< 0.001) (Figure 2f and Table 1). This suggests that long-term training may counteract the effect of aging on synthesis of this interleukin and maybe facilitates the homeostasis of hemopoietic system.
Insulin-like growth factor-I (IGF-I), growth hormone (GH), testosterone and dehydroepiandrosterone-sulfate have been reported to have anabolic effects on muscle and bone mass and to be associated with a globally increased physical and psychological well-being in elderly people . Circulating levels of these hormones usually decrease with male aging  but it is unclear whether this decrease is an unavoidable effect of aging itself or reflects the influences of modifiable external factors such as lifestyle. It is still uncertain whether habitual moderate physical activity may counteract the age-associated reduction in blood levels of endogenous anabolic hormones.
Few studies have focused on the relationship between these hormones and regular physical activity in older subjects. A recent study showed association of regular moderate physical activity with higher levels of DHEAS and IGF-I in aging men . In another study significant positive correlations between DHEAS and energy expenditure in both light physical activities and moderate intensity sports were found for elderly women but not for men . In that study, the DHEAS levels of elderly women were also correlated with maximal oxygen comsumption (VO2 max). On the other hand, Abbasi et al.  reported that the DHEAS values of older men (but not of older women) were associated with VO2 max but not with energy expenditure in physical activities. Others demonstrated a small increase in fasting level of IGF-I in men  and women . However, some studies have found no relation between regular physical activity and serum/plasma levels of IGF-I or GH [24–26]. Studies on older subjects have not shown significant chronic effects of high-intensity exercise on blood testosterone levels [25, 26].
Regular physical activity and serum hormone concentrations in elderly men (mean ± S.E.M.)
79 ± 6
92 ± 14
Free testosterone (pmol/l)
258.4 ± 15.5
271.6 ± 19.1
Total testosterone (ng/dl)
529 ± 41
456 ± 36
0.44 ± 0.12
0.68 ± 0.32
13.7 ± 0.6
13.2 ± 0.8
0.19 ± 0.01
0.19 ± 0.02
Possible links between endocrinosenescence and immunosenescence have been studied [5, 28–30]. The HPA axis has gained more attention because DHEA(S) have shown some immunomodulatory effects, specially on cytokines . Studies showed that DHEA inhibited the stimulated production of IL-6 by human PBMC  and spontaneous production of this interleukin by human splenocytes . They also noted an inverse relationship between DHEA(S) and serum IL-6 during aging in humans. However divergent results have also been obtained , indicating that the relationship between IL-6 and DHEA(S) in man is more complex than perhaps hitherto appreciated.
In the present study we did not find any correlation between DHEAS and serum IL-6 levels in elderly subjects. Poor correlation was observed between DHEAS and other cytokines measured. To our knowledge, this is the first study that tested the correlation between DHEAS and Th1 and Th2 type cytokines concomitantly in elderly men. No correlation was found between other hormones and cytokines. The contribution of hormones to immunosenescence does not seem to be so clear at least between 60 and 80 years old.
We conclude that highly conditioned elderly men seem to have relatively better preserved immune system than the sedentary elderly men. Regular endurance exercise can correct some detrimental immune changes of aging but does not seem to prevent endocrinosenescence.
All subjects gave written consent prior to their inclusion in the study.
The three test groups comprised 20 older recreational runners (age range: 61–80 years), 20 age-matched sedentary controls (age range: 60–75 years), and 10 young sedentary controls (age range: 23–34 years). The mean ages (±SEM) for the three groups were: 66.7 ± 1.0, 65.8 ± 0.9, and 26 ± 1.8 years, respectively. Only men were studied.
The active elderly subjects reported running an average of 54 ± 2 min.d-1, 4.3 ± 0.2 d.wk-1, covering a weekly distance of 38.7 ± 2.6 km (range: 25–60 km). Subjects had maintained this level of exercise for 23 ± 2 years.
The sedentary subjects were not engaged in any kind of physical activity of ≥15 minutes duration more than 3 times per week for the previous 2 years.
The maximal oxygen consumption (VO2 max) of these volunteers was measured. VO2 max was assessed by progressive and continuous testing on a treadmill until exhaustion, according to the Bruce protocol . All subjects reached their age-predicted maximal heart rate and maximal respiratory quotient (RQ ≥ 1.10). Oxygen uptake and ventilation were measured using a Vmax Series 229 metabolic cart (SensorMedics, Yorba Linda, CA-USA). The elderly runners presented a 52% higher VO2 max (38.5 ± 1.1 ml.kg-1.min-1) than the sedentary elderly subjects (25.5 ± 0.8 ml.kg-1.min-1), matching the level seen in sedentary young subjects (36.6 ± 2.1 ml.kg-1.min-1).
Subject selection was performed according to the SENIEUR protocol . Exclusion criteria included: systemic diseases, such as cardiac, liver, kidney and bone marrow disorders, diabetes, acute and chronic inflammatory conditions, clinical depression, neurodegenerative disease, anemia, leucopenia, alcoholism, and undernutrition. Subjects were excluded if they smoked and if they were taking any medications, vitamins or food supplements known to affect immune function. Recent (<3 months) surgery, infection, or vaccination and previous history of cancer or immune disorders were also considered exclusion criteria.
Blood specimens were collected from all subjects in the seated position between 7:00 and 8:00 h after resting for a minimum of 30 minutes and abstaining from all food, beverages (except water) for at least 8 h, and vigorous physical activity for at least 48 h.
Preparation of peripheral blood mononuclear cells (PBMC) and proliferative response
PBMC suspensions were prepared from heparinized venous blood using a Ficoll-Hypaque gradient, washed with RPMI 1640 medium, and resuspended in RPMI supplemented with 10% type AB human serum (Sigma, St Louis, MO-USA). Two × 106/ml cells per well were cultivated in triplicate in flat-bottomed 96-well plates for 3 days, at 37°C and 5% CO2, in the presence of 2.5 μg/ml phytohemagglutinin-A (PHA) (Difco Laboratories, Detroit, MI-USA) and 5 μg/ml anti-CD3 monoclonal antibodies (OKT3). Cultures containing no mitogens were used as controls. The cultures were pulsed with 0.5 μCi per well of [3H] thymidine (Amersham Pharmacia Biotech, Buckinghamshire, England) 18 hours prior to harvesting, and the amount of radioactivity incorporated was determined with a scintillation counter (1205 Betaplate, Wallac Oy, Turku, Finland). Proliferation values are presented in the form of stimulation index, calculated from the ratio radioactivity in stimulated culture to radioactivity in non-stimulated culture.
Cytokine production and serum cytokines
Culture supernatants were harvested by centrifugation after stimulation with PHA for 24 h, as described above. Supernatants were stored at -70°C until analysis in duplicates using a solid-phase sandwich ELISA kit (Quantikine; R & D Systems, Minneapolis, MN-USA).
Levels of IL-2, IL-3, IL-4, IL-6, IL-10 and IL-12 were measured. Results were expressed as pg/ml. The detection limits were: <0.7 for IL-2, <7.4 for IL-3, <10 for IL-4, <0.7 for IL-6, <3.9 for IL-10 and <5.0 for IL-12.
Serum cytokines levels were also determined in elderly subjects.
Measurement of serum hormone levels
Dehydroepiandrosterone sulfate was assayed by radioimmunoassay and growth hormone was assayed by immunofluorometric assay. Testosterone was assayed using an electrochemiluminescence immunoassay and free testosterone value was calculated from total testosterone and immunoassayed SHBG concentrations (SHBG, sex hormone-binding globulin). Cortisol was assayed using a fluoroimmunoassay. The intraassay and interassay coefficients of variation were below 7.5% and 8.0% in each test, respectively.
Serum hormone levels were measured only in elderly subjects.
Statistical analysis and power calculations were performed using the SigmaStat software (Jandel Scientific, San Rafael, CA-USA). Results are expressed as mean ± SEM. Group comparisons were made using a one-way ANOVA or Kruskal-Wallis test. For post-hoc multiple comparisons, a Tukey test or a Dunn procedure were made. Comparisons of the values between two groups were performed by Student t-test or Mann-Whitney rank sum test depending on the normality of the distribution curves. The correlation between two variables was analyzed by the Pearson correlation coefficient. The level of significance was set at p < 0.05.
This work was supported by a grant from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP). The authors express their gratitude to the staff of Laboratório de Investigação Médica (LIM-56) for technical assistance.
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