According to the results, during and after BFR training, many blood factors are activated and angiogenesis is stimulated in the arteries. The current study aimed to determine the effect of two eccentric resistance training methods with and without blood flow restriction on serum IL6 and MMP9 levels of active young men.
The results showed that a low-intensity resistance training session with blood flow restriction and also a high-intensity resistance training session without blood flow limitation did not have a significant effect on serum IL-6 serum levels. This result is consistent with the results of Larkin et al. (
7) and Item et al. (
8). And it is inconsistent with Melanouri and Mahdavi (
9).
High-intensity training can increase myoglobin, lipid peroxidase (LP), creatine kinase (CK), and cytokines (IL-6, TGF-β, TNF-α) in the short-term. Takarda et al. (
17) investigated the effects of BFR in combination with 20% 1RM resistance training on CK, LP, and IL-6 concentrations. After implementing the protocol for 90 minutes the IL-6 was increased and no change was observed in other variables (
17), which is inconsistent with the results of the current study. This inconsistency can be attributed to the type of performed protocol and the duration of the resistance exercise. Melanouri and Mahdavi (
9) reported an increase in skeletal muscle IL-6 following 17 sessions of resistance training in diabetic rats and Mir et al. (
10) reported a decrease in serum IL-6 followed by 8 weeks of resistance training in inactive middle-aged men.
In the study of Melanouri and Mahdavi (
9) the reason for increased interleukin and the lack of increase in this factor in the current study can be attributed to the characteristics of participants and the nature of the training course in which diabetic rats participated and the duration of the training course was 17 sessions, but in the present study the participants were active males and the duration of the training was one session. Also, decreased levels of serum IL-6 in the study of Mir et al. (
10) and its stability in the current study can be attributed to the characteristics of participants, the length of the training period, and the level of training, in which in the current study no active middle-aged males participated. The resistance training program was implemented for 8 weeks, but in our study, participants were active young man and their training program consisted of one resistance training session.
Most studies have used blood flow restriction during exercise. According to the literature, the type of cuff used may affect the results. In some studies, it has been used as an elastic cuff and in others as a non-elastic one. Rossow et al. (
18) investigated cardiovascular responses in the presence of restricted blood flow in resistance sports and reported that the type of limiting device had an effect on cardiovascular responses and should, therefore, be considered when designing studies. Yasuda et al. (
19) also showed that resistance training with an elastic band and blood pressure restriction did not have a negative effect on adult arterial stiffness and improved muscle cross-section and maximum strength. Also, these studies showed the effect of blood flow restriction on increasing the expression of genes affecting the process of angiogenesis in skeletal muscle tissue, while reported no effect on serum and protein levels of VEGF (
8).
Another study found an increase in MMP-9 marker levels in venous arteries during a training session, however, no MMP-9 analysis was observed in the studied muscles (
20). This increase was also observed at the end of eccentric sports activities and progressive step testing to the point of exhaustion (
11,
12), while in the present study a low-intensity resistance training session with high blood flow and high intensity on MMP-9 serum levels young active men was not different. Which is not consistent with previous studies.
Numerous studies have examined skeletal muscle as a source of increased circulating MMP-9 release. In some studies, only intravenous MMP-9 concentration is measured, and the increase observed in MMP-9 concentration reflects its release by skeletal muscle exercising. These data suggest that MMP-9 is less likely to increase circulation than other sources (other than skeletal muscle) (
11). MMP-9 is a diverse protease with a significant underlying panel, and it has been shown that different cell types can express and secrete MMp-9. On the other hand, MMP-9 has little basic expression in most tissues (
21). Laboratory studies have reported an increase in MMP-9 activation of post-exercise skeletal muscle (
20). MMP-9 also appears to be activated in post-workout muscle tendons (
22), which explains why the MMP-9 serum levels do not differ in two intensities in the present study. The most basic biological and basic function of MMP-9 is the breakdown of extracellular matrix proteins. Total levels of MMP-9 (pro-MMP-9 and active mmp-9) in skeletal muscle following exercise are significantly faster than pre-workout values. After exercise, it increases and stays at a high level for up to 120 minutes. Therefore, since MMP-9 is released by active muscles, MMP-9 is a potential candidate and an increase in MMP-9 circulatory levels following severe muscle damage is reported (
20).
So far, it has been shown that the age range of the participants was ranging from 20 to over 50 years old (
23) and these subjects with different physical fitness levels as some were untrained (
24), recreationally active (
25) and elites athletes (
17) in Practices have been recruited in pervious research. The effects of differences between men and women in BFR require further research and more study has been done on men.
However, it is not clear exactly how much blood flow restriction is enough to stimulate training response as in pervious studies is between 100 mmHg and 300 mmHg pressure in pneumatic cuff were applied to induced restricted or incomplete blockage of working muscle blood flow. Some studies have performed complete repetition at any time, while in others, the activity has been executed up to the fatigue (
17,
24,
26). In present study we applied 10 mm Hg above mean systolic blood pressure to induced about 50% blood flow restriction.
Takano et al. (
27) reported a significant increase in their indices at low pressures of 50 mmHg. Takano et al. (
27) observed a 30% reduction in arterial blood flow following a 160 to 180 mmHg blood flow restriction with a 33 mm cuff width. By increasing the cuff width (pressure relief tool), the required pressure to restrict blood flow was reduced (
3). In various studies, the width of the cuff varied from 5 to 20.5 cm. In the present study, which a 13 cm wide pneumatic band was used, the amount of pressure to apply the restriction of blood flow was 100 - 90 mmHg. Decreased blood flow reduced intramuscular oxygen and metabolic clearance, which led to the accumulation of lactic acid and the onset of fatigue, which is determined by a decrease in the tone and number of repetitions of a single resistance activity (
27,
28).
Overall, given that in the current study intense exercise, especially in high intensity (i.e. eccentric resistance training with about 80% - 70% MVC), did not induce a significant effect on serum levels of IL-6 and MMP-9 of active males, it can be argued that more intense exercise leads to the release and production of countless free radicals that in turn results in elimination or inactivation of nitric oxide (NO) produced, subsequently disrupted these process as nitric oxide is an important and effective factor in angiogenesis. One of the limitations of the present study is the short duration of eccentric resistance exercise executed by active male volunteers, which could be cleared in further studies.
5.1. Conclusions
Overall, the results of the present study showed that a low-intensity resistance exercise session with blood flow restriction, such as high-intensity resistance exercise session without blood flow restriction, can increase the serum levels of IL-6, which was not statistically significant. While decreased level of MMP-9 was not statistically significant among active males. These results can be attributed to the duration and intensity as well as the type of exercise protocol, number of times and repetition of courses, and physical fitness levels of the participants. Further studies are needed to identify the exact volume and modality of exercise required to stimulate optimum exercise-induced angiogenesis response.