Abstract
[Purpose] The aim of this study was to compare the differences in recovery periods after maximal concentric and eccentric exercises. [Subjects and Methods] Twenty-two participants voluntarily participated and were divided into two groups: the athlete and sedentary groups. An incremental treadmill running test was performed until exhaustion. During the subsequent passive recovery session, heart rate and venous blood lactate level were determined every 3 minutes until the venous blood lactate level reached 2 mmol/l. The same test protocol was implemented 15 days later. [Results] Both groups showed significantly shorter running durations in concentric exercise, while significant differences were found between the athlete and sedentary groups in terms of venous blood lactate level responses. In addition, there were significant differences between the athlete and sedentary groups in terms of running duration and heart rate in concentric and eccentric exercises. [Conclusion] The present study revealed no difference between the athlete and sedentary groups in terms of recovery durations after eccentric and concentric loadings, although the athletes demonstrated faster recovery in terms of HR compared with the sedentary group. It was thought that concentric exercises cause greater physiological responses.
Key words: Eccentric, Concentric, Recovery
INTRODUCTION
Recovery is defined as the process of normalization of the organism after workout1). After maximal exercise, the purpose of the recovery period is to rest the organism or return to conditions before the exercise. Recovery also accelerates the regeneration rate of the organism between training sessions and decreases fatigue and injury risk. Lactic acid accumulation is one of the important factors that causes fatigue. Therefore, recovery or resting starts with the decrease of lactic acid in the body. Removal of lactic acid, which is eliminated in blood and muscle, occurs over a period of approximately 2 hours with passive recovery and over a period of 1 hour on average with active recovery after maximal exercise1). Skeletal muscle contraction is classified in the literature as isometric contraction, concentric contraction, and eccentric contraction. In eccentric contraction, the load torque is greater than the muscle torque, and the muscle lengthens. In contrast, the muscle torque is greater than the load torque in concentric contraction, and the muscle length shortens2). Some studies in the literature have demonstrated that eccentric exercises lead to strength losses, while, others have shown different results because of the effects of exercise intensity, exercise type (resistance, downhill running), and area where the exercise is implemented3, 4). Studies have shown that blood lactate levels increase 6–10 folds during eccentric exercise5). In addition to this, it can therefore be seen that mechanical stress per fibril during eccentric exercises is higher than that during concentric exercise. However, concentric exercise also causes more energy expenditure, and it leads to more maximal contraction, lactic acid, and heart rate responses compared with eccentric loading6,7,8).
Eccentric contraction has been shown to produce greater muscle hypertrophy than a concentric contraction after resistance training9). In addition to greater hypertrophy, eccentric contraction training tends to exert lower stress on the cardiovascular system10). In contrast to eccentric training, the cardiovascular and metabolic responses show a linear increase in concentric running11). It has been stated that this difference can be associated with the contribution of gravity during eccentric exercise. Furthermore, it is understood that gravitational force increasingly assists with the work of performing the activity as the negative slope becomes steeper, thus reducing the physiologic work required of the body11). As a result of this, negative slope walking e.g., walking downhill may be associated with cardiovascular or metabolic stress11). The aim of this study was to compare the differences in recovery periods after maximal concentric and eccentric exercises between athletes and sedentary individuals.
SUBJECTS AND METHODS
The study was designed as a comparative study. All measurements were performed in the Department of Physiotherapy and Rehabilitation, Gazi University Faculty of Health Sciences, in a temperature-controlled performance laboratory. All participants were notified of the research procedures, requirements, benefits, and risks before giving informed consent. Written informed consent was obtained from all the participants. The study was approved by the research ethics committee of Gazi University and was conducted in a manner consistent with the institutional ethical requirements for human experimentation in accordance with the Declaration of Helsinki. All measurements were performed by the same researchers at a similar time of the day between 8:00 and 12:00 a.m. Participants were asked not to exercise exhaustively on the day prior to assessment and to have eaten and to be hydrated on the day of the test. After excluding chronic or acute health conditions, musculoskeletal system problems, and any drug intake, that might affect performance. Twenty-two participants were voluntarily participated. The participants were divided into two groups: the athlete group and the sedentary group. The athlete group trained on average 2 hours/day a least 4 days/week, whereas the sedentary group performed no training and had no lifestyle changes during the study.
All the players completed an incremental treadmill test on a motorized treadmill (Cosmed, Italy) at an incline of 10% until exhaustion. The test began at 8 km.h−1, and the speed was increased by 1 km.h−1 every 3 minute until exhaustion. The participants were verbally encouraged to give maximal effort during the test. Heart rate was monitored continuously throughout the test and passive recovery session with a Polar RS400 heart rate monitor (Polar, Finland). The heart rate data were transferred to a computer and smoothed (average of 1 second) by the Polar Precision Performance Software (PPP4, Finland). During the passive recovery session, the venous blood lactate level (La) was determined every 3 minutes until it reached 2 mmol/l. The same test protocol was implemented 15 days later. The data are reported as means and standard deviations. Differences in all test performance variables between the athlete and sedentary groups were by nonparametric Wilcoxon signed rank tests for independent samples. All statistical analyses were performed in SPSS version 16.0, and the level of statistical significance was set at p<0.05.
RESULTS
Table 1 shows the descriptive characteristics of the subjects.
Table 1. Descriptive characteristics of participants.
| Athlete | Sedentary | |
|---|---|---|
| Age (years) | 22.1 ± 3.3 | 20.1 ± 1.1 |
| Height (cm) | 176 ± 0.5 | 174 ± 0.0 |
| Weight (kg) | 73.4 ± 6.4 | 65.9 ± 8.6 |
| BMI (kg/m2) | 23.5 ± 1.2 | 21.8 ± 3.0 |
Table 2 shows comparisons of the running durations, recovery durations, post-recovery heart rates, and post-exercise lactic acid values within the groups. Significant differences were found between concentric and eccentric loading in the athlete group in terms of running duration (17.1 ± 0.9 vs. 45.0 ± 2.7; z=−2.80, p=0.00) and La values (10.8 ± 1.6 vs. 4.3 ± 1.2; z=−2.80, p=0.00). Similarly, significant differences were found between concentric and eccentric loading in the sedentary group in terms of running duration (10.8 ± 1.3 vs. 26.1 ± 0.9; z=−2.80, p=0.00) and La values (11.0 ± 2.4 vs. 5.7 ± 1.7; z=−2.80, p=0.00).
Table 2. Comparison of running durations, recovery durations, post-recovery heart rates, and post-exercise lactic acid values within the groups.
| Athlete (Concentric loading) (+10%) |
Athlete (Eccentric loading) (−10%) |
Sedentary (Concentric loading) (+10%) |
Sedentary (Eccentric loading) (−10%) |
|
|---|---|---|---|---|
| Running duration (min) | 17.1 ± 0.9 | 45.0 ± 2.7* | 10.8 ± 1.3 | 26.1 ± 0.9* |
| Recovery duration (min) | 40.1 ± 9.5 | 35.0 ± 18.9 | 41.3 ± 7.4 | 36.1 ± 20.3 |
| Heart rate (rate/min) | 80.1 ± 7.7 | 75.7 ± 6.6 | 101.9 ±11.9 | 100.1 ± 20.2 |
| Lactic acid (mmol/l) | 10.8 ± 1.6 | 4.3 ± 1.2* | 11.0 ± 2.4 | 5.7 ± 1.7* |
*p<0.05
Table 3 shows comparisons of the running durations, recovery durations, post-recovery heart rates, and post-exercise lactic acid values between the groups. Significant differences in concentric loading were found between the athlete and sedentary groups in terms of running duration (17.1 ± 0.9 vs. 10.8 ± 1.3; z=−3. 65, p=0.00) and post-recovery HR responses (80.1 ± 7.7 vs. 101.9 ± 11.9; z=−3.63, p=0.00). Similarly, significant differences in eccentric loading were found between the athlete and sedentary groups in terms of running duration (45.0 ± 2.7 vs. 26.1 ± 0.9; z=−3. 07, p=0.00) and post-recovery HR responses (75.7 ± 6.6 vs. 100.1 ± 20.2; z=−2.82, p=0.00).
Table 3. Comparison of running durations, recovery durations, post-recovery heart rates, and post-exercise lactic acid values between the groups.
| Athlete (Concentric loading) (+10%) |
Sedentary (Concentric loading) (+10%) |
Athlete (Eccentric loading) (−10%) |
Sedentary (Eccentric loading) (−10%) |
|
|---|---|---|---|---|
| Running duration (min) | 17.1 ± 0.9 | 10.8 ± 1.3* | 45.0 ± 2.7 | 26.1 ± 0.9* |
| Recovery duration (min) | 40.1 ± 9.5 | 41.3 ± 7.4 | 35.0 ± 18.9 | 36.1 ± 20.3 |
| Heart rate (rate/min) | 80.1 ± 7.7 | 101.9 ± 11.9* | 75.7 ± 6.6 | 100.1 ± 20.2* |
| Lactic acid (mmol/l) | 10.8 ± 1.6 | 11.0 ± 2.4 | 4.3 ± 1.2 | 5.7 ± 1.7 |
*p<0.05
DISCUSSION
The aim of this study was to compare the differences in recovery periods after maximal concentric and eccentric exercises. One of the main findings of the present study is that the post-exercise La responses are significantly higher with concentric loading compared with eccentric loadings. However, the athlete group had a significantly lower running duration with concentric loading. Both the athlete and sedentary groups tolerated eccentric loading better in terms of running durations and post-exercise lactic acid levels. As La and H+ are removed from blood via oxidation12), the type of the recovery significantly affects the elimination of La from blood13). Studies have repored that anaerobic energy metabolism, an important part of recovery session, is closely associated with the elimination of La from muscle and blood after high intensity activities14, 15). The elimination of La from muscle and blood after a maximal exercise occurs over a period of approximately 2 hours with passive rest and over a period of 1 hour on average with active rest1). Several studies have demonstrated that active recovery is a more effective strategy for eliminating of La from muscle and blood and subsequent exercise performance compared with other recovery strategies16,17,18). Active recovery allows greater reoxygenation of myoglobin and therefore oxygen delivery to the muscles19). Therefore, recovery strategies are of crucial importance for subsequent performance or loading after maximal or supramaximal loading.
Our results showed that no significant difference was observed in an intragroup comparison made between +10% and −10% slopes in post-exercise recovery durations and post-recovery HR of the athletes, while significant differences were detected in running durations and post-exercise La values in the athlete and control groups. This may explain why the athlete group tolerated exercise better in both loading types and they recovered more efficiently after the end of the exercise. A previous study showed that passive recovery strategies showed no advantages in recovery except for after high intensity exercise with a recovery period of less than 3 minutes20). For these reasons, active resting is advisable if the recovery period is longer than 3–4 minutes after high intensity exercise. Moreover, many studies have shown that elimination of La and post-exercise HR responses are correlated with aerobic capacity21). Low-intensity exercise effectively increases endurance capacity, but it does not effectively induce hypertrophy of the skeletal muscle22). In contrast, several studies have shown that capacity of the endurance affects muscle lactate concentration and lactate elimination after maximal loading23,24,25). Another study showed that the ability to eliminate lactate increases in workout endurance exercises during active recovery18). In addition, endurance exercises reduce lactate production and increase the removal of lactate26). In contrast, no differences were found between trained and sedentary people in terms of La during passive recovery after exhaustive exercise15). The results of that study are similar our study results. It is known that aerobic training, which improves maximal oxygen uptake and oxidative capacity, increases the activity of aerobic enzymes and mitochondrial and capillary densities in muscles27), is one of the most common and popular activities among adults of all ages, decreasing the resting HR5) and shortening the post-exercise recovery phase28). In addition, it was found that the recovery of HR within 30 seconds after exercise is negatively correlated with the pre-exercise levels29).
The present study also showed that running duration and post-recovery HR responses were significantly higher in after concentric loading in the athlete group compared with the sedentary group. Additionally, passive recovery had an effect on running duration and post-recovery HR responses, and the athlete group had a significantly lower running duration and post-recovery HR responses after eccentric loadings. This can be explained by the positive physiological effect on athletes of training for a long time. Many activities of daily living use muscle combinations that require the coordinated use of concentric and eccentric contractions11). However, it is known that long-term eccentric contractions generate acute pains and reduction in functional strength in the sedentary individuals. Nevertheless, it can be possible to continue exercise, especially exercise in the form of downhill running for a long time without tiring with the contribution of gravity11). After two different styles of aerobic loading, that is, walking and jogging for men and women on −5% and −10% and +5% and +10% slopes respectively, were found lower heart rates responses found for both groups on the 5% and −10% slopes30). Both the athlete and sedentary groups continued the running exercise on the −10% slopes under eccentric loading for longer and completed running with a lower lactic acid level in our study as well.
In conclusion, athletes continued to exercises for a longer duration at a higher intensity under both concentric and eccentric loading. It was observed that concentric exercise led to more La accumulation and higher HR responses. Although there was no difference between the athlete and sedentary groups as a result of eccentric and concentric loadings in terms of recovery durations, it was observed that athletes recovered faster in terms of HR. In addition, both the athlete and sedentary groups performed eccentric running for longer under all loading conditions. La values were found to be lower in eccentric exercise. This fact demonstrates that athletes tolerate eccentric exercise better due to the contribution of gravity. The contribution of regular aerobic workouts to the recovery period was demonstrated in this study. However, it was observed that these effects were limited with a passive recovery period. Further studies are required to compare different recovery types and different loading programs. The results of this study suggest that people who wish to derive more benefits from training should pay special attention to choosing the exercise type and should consider their health profile. In addition, eccentric exercises are more effective for improving muscle size and gaining strength in healthy individuals.
REFERENCES
- 1.Fox E: The physiological basis of physical education and athletics, 4th ed. Philadelphia: Saunders College Publishing. [Google Scholar]
- 2.Tsumiyama W, Oki S, Takamiya N, et al. : Induction of muscle hypertrophy in rats through low intensity eccentric contraction. J Phys Ther Sci, 2014, 26: 1623–1625. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Eston RG, Finney S, Baker S, et al. : Muscle tenderness and peak torque changes after downhill running following a prior bout of isokinetic eccentric exercise. J Sports Sci, 1996, 14: 291–299. [DOI] [PubMed] [Google Scholar]
- 4.Evans WJ, Meredith CN, Cannon JG, et al. : Metabolic changes following eccentric exercise in trained and untrained men. J Appl Physiol 1985, 1986, 61: 1864–1868. [DOI] [PubMed] [Google Scholar]
- 5.Yamamoto K, Miyachi M, Saitoh T, et al. : Effects of endurance training on resting and post-exercise cardiac autonomic control. Med Sci Sports Exerc, 2001, 33: 1496–1502. [DOI] [PubMed] [Google Scholar]
- 6.Borg GA: Psychophysical bases of perceived exertion. Med Sci Sports Exerc, 1982, 14: 377–381. [PubMed] [Google Scholar]
- 7.Hedayatpour N, Falla D, Arendt-Nielsen L, et al. : Motor unit conduction velocity during sustained contraction after eccentric exercise. Med Sci Sports Exerc, 2009, 41: 1927–1933. [DOI] [PubMed] [Google Scholar]
- 8.Yu J: Comparison of lower limb muscle activity during eccentric and concentric exercises in runners with achilles tendinopathy. J Phys Ther Sci, 2014, 26: 1351–1353. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Farthing JP, Chilibeck PD: The effects of eccentric and concentric training at different velocities on muscle hypertrophy. Eur J Appl Physiol, 2003, 89: 578–586. [DOI] [PubMed] [Google Scholar]
- 10.Okamoto T, Masuhara M, Ikuta K: Cardiovascular responses induced during high-intensity eccentric and concentric isokinetic muscle contraction in healthy young adults. Clin Physiol Funct Imaging, 2006, 26: 39–44. [DOI] [PubMed] [Google Scholar]
- 11.Navalta JW, Sedlock D, Kyung-Shin P: Physiological responses to downhill walking in older and younger individuals. J Exerc Physiol. 2004, 7: 45–51. [Google Scholar]
- 12.Mazzeo RS, Brooks GA, Schoeller DA, et al. : Disposal of blood [1-13C] lactate in humans during rest and exercise. J Appl Physiol 1985, 1986, 60: 232–241. [DOI] [PubMed] [Google Scholar]
- 13.Gupta S, Goswami A, Sadhukhan AK, et al. : Comparative study of lactate removal in short term massage of extremities, active recovery and a passive recovery period after supramaximal exercise sessions. Int J Sports Med, 1996, 17: 106–110. [DOI] [PubMed] [Google Scholar]
- 14.Sahlin K, Henriksson J: Buffer capacity and lactate accumulation in skeletal muscle of trained and untrained men. Acta Physiol Scand, 1984, 122: 331–339. [DOI] [PubMed] [Google Scholar]
- 15.Oosthuyse T, Carter RN: Plasma lactate decline during passive recovery from high-intensity exercise. Med Sci Sports Exerc, 1999, 31: 670–674. [DOI] [PubMed] [Google Scholar]
- 16.Ahmaidi S, Granier P, Taoutaou Z, et al. : Effects of active recovery on plasma lactate and anaerobic power following repeated intensive exercise. Med Sci Sports Exerc, 1996, 28: 450–456. [DOI] [PubMed] [Google Scholar]
- 17.Jemni M, Sands WA, Friemel F, et al. : Effect of active and passive recovery on blood lactate and performance during simulated competition in high level gymnasts. Can J Appl Physiol, 2003, 28: 240–256. [DOI] [PubMed] [Google Scholar]
- 18.Taoutaou Z, Granier P, Mercier B, et al. : Lactate kinetics during passive and partially active recovery in endurance and sprint athletes. Eur J Appl Physiol Occup Physiol, 1996, 73: 465–470. [DOI] [PubMed] [Google Scholar]
- 19.Dupont G, Blondel N, Berthoin S: Performance for short intermittent runs: active recovery vs. passive recovery. Eur J Appl Physiol, 2003, 89: 548–554. [DOI] [PubMed] [Google Scholar]
- 20.Buchheit M, Laursen PB: High-intensity interval training, solutions to the programming puzzle: Part I: cardiopulmonary emphasis. Sports Med, 2013, 43: 313–338. [DOI] [PubMed] [Google Scholar]
- 21.Fox LE, Bowers RW, Foss ML: The physiological base or exercise and sport, 5th ed. Madison: Brown and Benmark, 1993. [Google Scholar]
- 22.Kraemer WJ, Gordon SE, Fleck SJ, et al. : Endogenous anabolic hormonal and growth factor responses to heavy resistance exercise in males and females. Int J Sports Med, 1991, 12: 228–235. [DOI] [PubMed] [Google Scholar]
- 23.MacRae HS, Dennis SC, Bosch AN, et al. : Effects of training on lactate production and removal during progressive exercise in humans. J Appl Physiol 1985, 1992, 72: 1649–1656. [DOI] [PubMed] [Google Scholar]
- 24.Thomas C, Sirvent P, Perrey S, et al. : Relationships between maximal muscle oxidative capacity and blood lactate removal after supramaximal exercise and fatigue indexes in humans. J Appl Physiol 1985, 2004, 97: 2132–2138. [DOI] [PubMed] [Google Scholar]
- 25.Dubouchaud H, Butterfield GE, Wolfel EE, et al. : Endurance training, expression, and physiology of LDH, MCT1, and MCT4 in human skeletal muscle. Am J Physiol Endocrinol Metab, 2000, 278: E571–E579. [DOI] [PubMed] [Google Scholar]
- 26.Bergman BC, Wolfel EE, Butterfield GE, et al. : Active muscle and whole body lactate kinetics after endurance training in men. J Appl Physiol 1985, 1999, 87: 1684–1696. [DOI] [PubMed] [Google Scholar]
- 27.Chtara M, Chamari K, Chaouachi M, et al. : Effects of intra-session concurrent endurance and strength training sequence on aerobic performance and capacity. Br J Sports Med, 2005, 39: 555–560. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Imai K, Sato H, Hori M, et al. : Vagally mediated heart rate recovery after exercise is accelerated in athletes but blunted in patients with chronic heart failure. J Am Coll Cardiol, 1994, 24: 1529–1535. [DOI] [PubMed] [Google Scholar]
- 29.Sugawara J, Murakami H, Maeda S, et al. : Change in post-exercise vagal reactivation with exercise training and detraining in young men. Eur J Appl Physiol, 2001, 85: 259–263. [DOI] [PubMed] [Google Scholar]
- 30.Pivarnik JM, Sherman NW: Responses of aerobically fit men and women to uphill/downhill walking and slow jogging. Med Sci Sports Exerc, 1990, 22: 127–130. [PubMed] [Google Scholar]
