1. Background
Nurses are so active and working hard, and their physical health guarantees better service to patients. The physical health of nurses is at risk due to persistent stress and long-term insomnia. Exercise at different times of the morning or evening can improve the mood status and reduce depression (1). Stress and lack of sleep weaken the immune system and disrupted hormones that are associated with sleep. Hormones of GH and IGF-1 are increased at night when there is no psychological tension and during physical activity (2).
Insulin-like growth factor (IGF-1) plays a key role in regulating growth and muscle development after birth (1, 2). This factor also plays a role in certain diseases such as muscular dystrophy, delayed wound tissue, and impair in the tissue of internal organs in the body (3, 4). Hence reinforcing the growth factor can prevent and even help treat some growth-related disorders. Moreover, IGF-1 is the most important family member of somatomedin that plays an important role in physical growth, proliferation, cell differentiation, metabolism, and life (5).
This factor plays a crucial role in the development of embryonic and fetal, and postnatal growth and increases tissue repair and anabolism in the elderly (6). Full IGF-1 contains 70 amino acids and is connected to binding proteins in plasma circulating insulin-like growth factor-binding proteins (IGFBPs). The main source of IGF-1 is the liver. One of the main mechanisms for the production of IGF-1 is the effect of GH on the liver to produce IGF-1. Other tissues, such as muscle, brain, and bones, also produce IGF-1. Owing to its central role in metabolic processes, this study continues in connection with the growth factor (7).
Furthermore, IGF-1 plays important roles in the adaptation of muscle hypertrophy to resistance exercise (8, 9), the growth and bone health (10), short-term and long-term metabolic activity (11), and adaptation of the organism to exercise (1). Limited researches have shown the central role of GH/IGF-1 in response to the adverse intermittent exercise. Exercise stimulates the release of growth hormone, but there are conflicting data about the effect of acute exercise on IGF-1 and GH.
Some studies attributed the rising of IGF-1 after exercise to the insulin-like effects. Some studies have reported a relationship between IGF-1 in blood circulation and muscle mass (12). Hasani-Ranjbaret al. (7) showed that an adverse intermittent training session increases the concentration of IGF-1 and its affiliates like IGFBP3.
Stokes et al. (12) examined the effect of aerobic adverse exercise values on IGF-1, IGF-2 growth hormones. The training protocol was 30 seconds faster, bicycling on ergometer cycling with the strength of 7 or 9 percent of body weight. Stokes et al. (2010) examined the effect of aerobic adverse exercise values on IGF-1 and IGF2 growth hormone. The training protocol was 30 seconds faster bicycling on ergometer cycling with the strength of 7 or 9 percent of body weight. The results of this research showed that one session of adverse exercise stimulates GH release and has had no significant effect on IGF-1 and IGF2 concentration and IGF biological activity (12). Some other studies show a drastic incremental change increase (2, 8, 10), while some studies reported a decrease (13), and several studies reported no significant differences (11, 14). Some studies have reported the independence of these two hormones (15).
2. Objectives
According to the results of various studies and the release of IGF-1 from different tissues, it is not yet clear whether the increase in IGF-1 secretion occurs after exercise and follows an increase in GH or its increase is independent of the increase in GH. Also, because most research has been done on men and there is a difference between women’s and men’s hormonal responses to a different exercise; hence, the purpose of the study was to examine the effect of two types of intermittent exercise on GH and IGF-1 serum in severely overweight nurses.
3. Methods
The present research is quasi-experimental, and subjects were randomly divided into different training groups of two groups of adverse intermittent exercise (HIIT) and a control group (C).
3.1. Participants
The study population consisted of female nurses in Amir Al-Momenin Hospital in Gerash City. The study was conducted according to the Declaration of Helsinki. On a certain day, the volunteers were invited, and after presenting full comments on the process of the study and the benefits and potential harms of the study, written informed consent was obtained from volunteers. The participants were informed about the confidentiality of their information. They were also ensured that they could withdraw from the study whenever they desired. The inclusion criteria were the BMI index between 23 and 24.5, the ability to perform physical activity, and having no underlying disease. The exclusion criteria were unwillingness to continue the activity and a doctor’s diagnosis.
3.2. Study Design
Twenty-seven participants were selected to participate in the study using the convenience sampling method who were divided into three groups, including adverse intermittent exercise type 1 (eight seconds quick running and twelve seconds of active recovery), adverse intermittent exercise type 2 (sweep test with a maximum speed of 40 meters) and the control group (nine participants per group) (Figure 1). Before choosing the sample to the desired height, their weight, body fat percentage, BMI, and waist to hip ratio were measured to provide homogenous groups. The average age, height, and weight of groups were 25.81 ± 60 years old, 158.01 ± 67 cm, and 69.41 ± 25 kg. Also, the average BMI of the subjects was 29.11 ± 3.94 (kg/m2). Pre- and post-test were taken from all subjects.
Figure 1.
Flow chart of the study
3.3. Training Protocol
To do the exercise, the subjects were randomly assigned to three groups (two groups of adverse intermittent exercise (HIIT) and control group (C). Experimental group 1 for four weeks and three sessions per week had exercises that include eight seconds of rapid running and twelve seconds of active recovery (walk) at the determined time in the evening (5 PM). This exercise protocol was piloted before the start of the study. At the same time, experimental group 2 conducted the exercise protocol of a maximum speed of 40 m derived from the sweep test of 40 meters with a maximum speed of three sessions per week for four weeks and were as follows (Figure 2).
Figure 2.
HIIT exercise protocol of the study
Starting with the exercise protocol, subjects ran with a maximum speed of start point (cone no.: 1) to the cone (2) (route A), then turn in the opposite direction with a maximum speed of 20 km to the cone (3) (route B) and then again returned to the starting point (cone (1)) with a maximum running speed (line C) to a distance of 40 meters (12).
3.4. Measurements
Twenty-four hours before the first practice session and 24 hours after the last section, 10 cc blood sample was taken from the brachial vein (antecubital) of all subjects in eight hours fasting status (8:30 AM). Blood samples were immediately poured into tubes containing EDTA (Ethylene Diamine Tetra Acetate) anticoagulant. Then were centrifuged at 3,000 rpm for 10 min at 4°C. Serum GH levels were used by the ELISA method and using specific ELISA kit (manufactured by Mediagnost Germany), and ELISA kit (manufactured by Koma Biotech) was used to measure IGF-1 according to the manufacturer’s instructions (11). We calculated BMI using the formula of weight (kg) that is divided by height square (m2). We calculated the percentage of fat using a body composition machine. Height and weight were calculated using SECA standard gauge and scale, respectively (12).
3.5. Statistical Analysis
The normality of the collected data was checked by the Kolmogorov-Smirnov test (KS). The value of P is considered to be at 0.05, and the calculations were performed using SPSS software version 16. An independent t-test was used to compare the mean values of groups studied, according to the study design.
4. Results
Twenty-seven nurses (mean age 25.81 ± 60 year, height 158.01 ± 67 cm, and weight 69.41 ± 25 kg) have voluntarily participated in this study. The results of general variables (BMI, height, weight, body fat percentage, and waist to hip ratio) and studied variables (GH and IGF-1) are presented in tables 1 and 2.
Table 1.Anthropometric Variables of Subjects Before and After the Interventionala
| Variables | Experimental Group 1 | Experimental Group 2 | Control Group | |||
|---|---|---|---|---|---|---|
| Pre-Test | Post-Test | Pre-Test | Post-Test | Pre-Test | Post-Test | |
| Age, y | 25.71 ± 63 | 25.91 ± 57 | 25.81 ± 60 | |||
| Height, cm | 162.70 ± 67 | 163.28 ± 67 | 162.99 ± 67 | |||
| Weight, kg | 61.40 ± 39 | 61.11 ± 39 | 61.31 ± 14 | 61.30 ± 39 | 61.52 ± 25 | 61.54 ± 39 |
| BMI, kg/m2 | 23.11 ± 3.9 | 23.14 ± 2.1 | 24.15 ± 3.6 | 24.11 ± 2.4 | 23.45 ± 1.8 | 23.44 ± 5.6 |
| Waist | 97.23 ± 1.4 | 94.80 ± 2.2 | 98.09 ± 3.3 | 96.42 ± 4.1 | 99.18 ± 2.6 | 98.70 ± 6.9 |
| WHR, ratio | 0.779 | 0.777 | 0.770 | 0.771 | 0.759 | 0.755 |
| Body fat, % | 22.98 | 18.97 | 23.08 | 20.08 | 23.33 | 23.71 |
Abbreviation: BMI, body mass index; WHR, waist/hip ratio.
aValues were presented as mean ± SD unless otherwise indicated.
Table 2.Changes of Variables (GH and IGF-1) in the Experimental and Control Groups Before and After 4 Weeks of HIITa
| Variables | Groups | Pretest | Posttest | Difference | P Value |
|---|---|---|---|---|---|
| GH, μg/mL | Experimental 1 | 6.01 ± 14.02 | 16.73 ± 3.24 | 10.72 | 0.010b |
| Experimental 2 | 5.98 ± 5.32 | 10.04 ± 1.61 | 4.06 | 0.032b | |
| Control | 6.23 ± 9.21 | 6.24 ± 9.89 | 0.01 | 0.496 | |
| IGF-1, ng/mL | Experimental 1 | 278.64 ± 4.03 | 356.1 ± 7.27 | 77.46 | 0.013b |
| Experimental 2 | 275.63 ± 7.91 | 290.54 ± 3.12 | 14.91 | 0.004b | |
| Control | 280.60 ± 2.44 | 280.68 ± 1.2 | 0.08 | 0.076 |
aValues were presented as mean ± SD.
bP < 0.05 is accepted to be statistically significant.
Research findings showed that GH concentration increased significantly after performing HIIT for four weeks in 1 and 2 training group (P = 0.032 in group 2 and P = 0.010 in group 1) (Table 2), but no significant changes in the levels of GH were observed in the control group (Table 2). Also, the concentration of IGF-1 level increased significantly in the exercise group 1 and 2 (P = 0.004 in group 2 and P = 10.013 in group 1), while the control group showed no significant changes in IGF-1 levels (Table 2). Body fat percentage was reduced in both groups significantly, while none of the waist-to-hip ratio (WHR), BMI, and weight variables showed significant changes in the three groups.
5. Discussion
Growth hormone secreted from anterior pituitary cells stimulates IGF-1 secretion from liver cells and ultimately stimulates protein anabolic and fat breakdown. Moreover, HIIT exercises stimulate the breakdown of adipose tissue, resulting in weight loss and improved health indicators. Therefore, it is important to examine the effect of these exercises on these two growth factors. Weight training, BMI, and WHR had little effect, but both exercises reduced body fat by 3 to 4 percent. The reason for the slight decrease in the first three factors and the further decrease in body fat percentage is the replacement of muscle mass with fat mass. The results of the present research about the significant increase in GH and IGF-1 are in line with the results of Tanimotoet al. (11) and Maniniet al. (16) and is different from the results of Kim et al. (3). The reason for this difference could be the type of program and the duration of the exercise. In some studies, the GH levels increased after adverse intermittent exercise (5, 8, 17).
The intensity of the training was close in all of these studies, so the reason for the difference in results was probably the length of the training period. Based on the evidence available, the mechanism of IGF-1 response in circulating to adverse intermittent exercise in studies is different (4). The results of this study are associated with IGF-1 response to adverse intermittent exercise, which are consistent with the results of Fujita et al. (4), while is different from the results of Takano (18). The reason for this difference seems to be the type of subjects (18).
The sharp rise in GH could not be due to the increase IGF-1 immediately after exercise because the level of IGF-1 even 16 to 28 hours after the release of GH peak is not reached (19). In the present study, an increase in serum levels of IGF-1 was not observed even to 5.1 times compared to the pre-workout. Although there are significant differences between the groups in terms of IGF-1 levels, the inter-group analysis showed a significant difference in the group of moderate-intensity resistance training.
Never the less, compared to previous studies that showed a 10 to 30-fold increase in serum IGF-1 serum after exercise, the low increase in serum IGF-1 in the present study was due to the measurement of hormone levels before reaching its peak time. In general, based on the results of this study, although the pattern of change in serum levels of GH and IGF-1 was similar in both groups, adverse intermittent exercise protocols with less intensity can cause a further increase in anabolic hormones in young girls is high-intensity resistance training. Selection of girl groups is due to the homogeneity of the objects in terms of all aspects of physiological and structural variables, and the goal of the researchers was to compare the differences between the two types of exercise, not the difference in results between the two genders. Owing to the limitations of research in the women’s community and the higher prevalence of obesity and overweight in women than men, this study was conducted on women (20, 21). The limitations of the study were the lack of control over diet, sleep, and emotional states of the subjects during exercise. It is recommended that this study should be performed in a group of men to achieve better results. In addition to the blood factors taken, several functional factors should be measured to evaluate the functional effects of these activities. However, due to limited research on the impact of HIIT on GH/IGF-1 in young nurses, more research is needed in this area.
5.1. Conclusions
Based on the findings of the present study, it seems that applying four weeks of high-intensity interval training (HIIT) is a suitable training method to increase the concentration of serum GH and IGF-1 and reduced the percentage of body fat in overweight young nurses and the response rate varies according to the intensity of the training protocol. Also, the intensity of exercise as a crucial factor in increased serum concentrations of GH and IGF-1 in response to exercise can be noted.
