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Responses of asthmatic and non-asthmatic athletes to prolonged treadmill running.

Metabolic and cardio-respiratory responses of four asthmatic and four non-asthmatic athletes to two hours of treadmill running at 70 percent of maximal oxygen uptake are compared. The asthmatic group had pre-exercise airflow obstruction, as indicated by the lower forced expiratory volume in one second (FEV1) even after medication (2.90 +/- 0.661) compared to the non-asthmatic group (4.09 +/- 1.331). Changes in blood lactate, glucose and catecholamine concentrations as a result of the two hour run were similar for the two groups. However, the pattern of breathing was different. The asthmatics had a slower breathing frequency but a similar tidal volume to the non-asthmatics. Both groups had an increase in the ventilation rate over the two hour run. For the non-asthmatic group, this increase in ventilation was achieved by an increase in the breathing frequency (p less than 0.01), whereas tidal volume was reduced (p less than 0.05). The increase in the ventilation rate over the two hour run for the asthmatic group was brought about by a small increase in breathing frequency (p less than 0.05), whereas tidal volume was not changed. This maintenance of the tidal volume by the asthmatic athletes during endurance running may compensate for the airflow obstruction, and so allow successful participation in endurance running.

Adaptation, Physiological↗

A systematic review of interventions to prevent lower limb soft tissue running injuries.

OBJECTIVES: To assess the available evidence for preventive strategies for lower limb soft tissue injuries caused by running. METHODS: An electronic database search was conducted using The Cochrane Musculoskeletal Injuries Group Specialised Register, The Cochrane Controlled Trials Register, Medline, Embase, Sport Discus, Heracles, Atlantes, Biosis, Cinahl, Scisearch, Current Contents, Index To Theses and Dissertation Abstracts. Any randomised or quasi-randomised trials evaluating interventions to prevent running injuries to lower limb soft tissue were included. The eligibility of trials for inclusion and the quality of the trials were independently assessed by two reviewers. RESULTS: Exposure to a high training load (duration, frequency, or running distance) increases the risk of injury, and thus modification of the training schedule can reduce the incidence of injury. The effectiveness of stretching exercises and of insoles in the prevention of lower extremity soft tissue injuries caused by running is not known. Wearing a knee brace with a patellar support ring may be effective in the prevention of anterior knee pain caused by running. CONCLUSIONS: This review provides evidence for the effectiveness of the modification of training schedules in reducing lower limb soft tissue running injuries. More studies are required to quantify the optimal training loads and to confirm that knee braces can prevent knee pain. It is important to note that the studies included in this review had few female participants therefore the results may not be generalisable.

Adolescent↗

Is excessive running predictive of degenerative hip disease? Controlled study of former elite athletes.

OBJECTIVE: To determine the effects of regular long distance running on the state of the hips in later life. DESIGN: Retrospective study of a cohort of elite athletes and a group of normal, healthy, untrained controls examined 15 years after initial testing. SETTING: Research project at school for physical education and sports. SUBJECTS: 27 Former long distance runners (mean age 42), nine former bobsleigh riders (mean age 42), and 23 normal, healthy, untrained men (mean age 35) who had been examined in 1973 and who agreed to re-examination in 1988. MAIN OUTCOME MEASURE: Radiological evidence of degenerative hip disease in 1988. RESULTS: Physiological and exercise characteristics of all subjects had been recorded in 1973, and in 1988 these measurements were repeated together with radiological examination of the hips. An additive radiological index of hip disease based on grades of subchondral sclerosis, osteophyte formation, and joint space narrowing was significantly increased among runners as compared with bobsleigh riders and untrained controls. After adjustment for age the significant effect of type of sports activity remained (p = 0.032). In multivariate analyses age and milage run in 1973 (97 km/week) emerged as independent, significant, and positive predictors of radiological signs of degenerative hip disease in 1988 (p = 0.017 and p = 0.024 respectively). Among runners alone running pace in 1973 rather than milage run was the stronger predictor of subsequent degenerative hip disease. The milage run in 1988 was not particularly predictive of the radiological index, but endurance in 1988 was inversely related to degenerative hip disease seen radiologically. CONCLUSION: Long term, high intensity, high milage running should not be dismissed as a potential risk factor for premature osteoarthritis of the hip.

Age Factors↗

Changes in blood lactate and heart rate in thoroughbred horses during swimming and running according to their stage of training.

The purpose of this study was to investigate whether the change in the performance capacity of horses trained by running could be evaluated with a standardised swimming exercise test as well as by a standardised running exercise test. Seven two-year-old thoroughbred horses were trained by running for four months and were subjected to a standardised swimming exercise tolerance test before the training began and after two and four months of training in addition to the standardised running tolerance test after two and four months of training. The running training brought about a significant change in the correlation between the swimming speed of the horses and their blood lactate concentration, and the correlation between the blood lactate concentration and maximum heart rate and running speed also changed significantly after two months of training.

Animals↗

Time spent at a high percentage of VO2max for short intermittent runs: active versus passive recovery.

The purpose of this study was to compare the effects of recovery type (active vs. passive) on the time spent at VO(2)max and above 90 % of VO(2)max during short intermittent runs (15 s) at 120 % of maximal aerobic speed. Twelve male subjects performed a graded test and intermittent runs (15 s) alternated with 15 s of active recovery (50 % of maximal aerobic speed) or with 15 s of passive recovery to exhaustion. The time to exhaustion during the intermittent runs with active recovery (445 +/- 79 s) was significantly shorter (p < 0.001) compared with passive recovery (745 +/- 171 s). No significant difference was found between time spent at VO(2)max and above 90 % of VO(2)max for intermittent runs alternated with active recovery (180 +/- 121 s and 282 +/- 117 s, respectively ) and intermittent runs alternated with passive recovery (191 +/- 135 s and 317 +/- 132 s, respectively ). The times spent at VO(2)max (p < 0.05) and above 90 % of VO(2)max (p < 0.001), expressed in percentage of time to exhaustion, were significantly longer for intermittent runs alternated with active recovery (41 +/- 27 % and 64 +/- 24 %, respectively) than with passive recovery (25 +/- 16 % and 43 +/- 16%, respectively). In conclusion, the present study has shown that the time to exhaustion during repeated high-intensity exercise was significantly greater for passive compared with active recovery, despite no difference in absolute time spent at a high percentage of VO(2)max. However, the time spent at a high percentage of VO(2)max, expressed as a percentage of time to exhaustion, was significantly higher for active compared with passive recovery.

Adult↗

Effects of beta-hydroxy-beta-methylbutyrate on muscle damage after a prolonged run.

This study examined the effects of supplemental beta-hydroxy-beta-methylbutyrate (HMB) on muscle damage as a result of intense endurance exercise. Subjects (n = 13) were paired according to their 2-mile run times and past running experience. Each pair was randomly assigned a treatment of either HMB (3 g/day) or a placebo. After 6 wk of daily training and supplementation, all subjects participated in a prolonged run (20-km course). Creatine phosphokinase and lactate dehydrogenase (LDH) activities were measured before and after a prolonged run to assess muscle damage. The placebo-supplemented group exhibited a significantly greater (treatment main effect, P = 0.05) increase in creatine phosphokinase activity after a prolonged run than did the HMB-supplemented group. In addition, LDH activity was significantly lower (treatment main effect, P = 0.003) with HMB supplementation compared with the placebo-supplemented group. In conclusion, supplementation with 3.0 g of HMB results in a decreased creatine phosphokinase and LDH response after a prolonged run. These findings support the hypothesis that HMB supplementation helps prevent exercise-induced muscle damage.

Adult↗

Relationship between fat-to-fat-free mass ratio and decrements in leg strength after downhill running.

The purpose of this study was to determine whether greater body fat mass (FM) relative to lean mass would result in more severe muscle damage and greater decrements in leg strength after downhill running. The relationship between the FM-to-fat-free mass ratio (FM/FFM) and the strength decline resulting from downhill running (-11% grade) was investigated in 24 male runners [age 23.4 +/- 0.7 (SE) yr]. The runners were divided into two groups on the basis of FM/FFM: low fat (FM/FFM = 0.100 +/- 0.008, body mass = 68.4 +/- 1.3 kg) and normal fat (FM/FFM = 0.233 +/- 0.020, body mass = 76.5 +/- 3.3 kg, P < 0.05). Leg strength was reduced less in the low-fat (-0.7 +/- 1.3%) than in the normal-fat individuals (-10.3 +/- 1.5%) 48 h after, compared with before, downhill running (P < 0.01). Multiple linear regression analysis revealed that the decline in strength could be predicted best by FM/FFM (r2 = 0.44, P < 0.05) and FM-to-thigh lean tissue cross-sectional area ratio (r2 = 0.53, P < 0.05), with no additional variables enhancing the prediction equation. There were no differences in muscle glycogen, creatine phosphate, ATP, or total creatine 48 h after, compared with before, downhill running; however, the change in muscle glycogen after downhill running was associated with a higher FM/FFM (r = -0.56, P < 0.05). These data suggest that FM/FFM is a major determinant of losses in muscle strength after downhill running.

Adenosine Triphosphate↗

Metabolic energy and muscular activity required for leg swing in running.

The metabolic cost of leg swing in running is highly controversial. We investigated the cost of initiating and propagating leg swing at a moderate running speed and some of the muscular actions involved. We constructed an external swing assist (ESA) device that applied small anterior pulling forces to each foot during the first part of the swing phase. Subjects ran on a treadmill at 3.0 m/s normally and with ESA forces up to 4% body weight. With the greatest ESA force, net metabolic rate was 20.5% less than during normal running. Thus we infer that the metabolic cost of initiating and propagating leg swing comprises approximately 20% of the net cost of normal running. Even with the greatest ESA, mean electromyograph (mEMG) of the medial gastrocnemius and soleus muscles during later portions of stance phase did not change significantly compared with normal running, indicating that these muscles are not responsible for the initiation of leg swing. However, with ESA, rectus femoris mEMG during the early portions of swing phase was as much as 74% less than during normal running, confirming that it is responsible for the propagation of leg swing.

Adult↗

Motor patterns in human walking and running.

Despite distinct differences between walking and running, the two types of human locomotion are likely to be controlled by shared pattern-generating networks. However, the differences between their kinematics and kinetics imply that corresponding muscle activations may also be quite different. We examined the differences between walking and running by recording kinematics and electromyographic (EMG) activity in 32 ipsilateral limb and trunk muscles during human locomotion, and compared the effects of speed (3-12 km/h) and gait. We found that the timing of muscle activation was accounted for by five basic temporal activation components during running as we previously found for walking. Each component was loaded on similar sets of leg muscles in both gaits but generally on different sets of upper trunk and shoulder muscles. The major difference between walking and running was that one temporal component, occurring during stance, was shifted to an earlier phase in the step cycle during running. These muscle activation differences between gaits did not simply depend on locomotion speed as shown by recordings during each gait over the same range of speeds (5-9 km/h). The results are consistent with an organization of locomotion motor programs having two parts, one that organizes muscle activation during swing and another during stance and the transition to swing. The timing shift between walking and running reflects therefore the difference in the relative duration of the stance phase in the two gaits.

Adult↗

Interaction of arch type and footwear on running mechanics.

BACKGROUND: Running shoes are designed to accommodate various arch types to reduce the risk of lower extremity injuries sustained during running. Yet little is known about the biomechanical changes of running in the recommended footwear that may allow for a reduction in injuries. PURPOSE: To evaluate the effects of motion control and cushion trainer shoes on running mechanics in low- and high-arched runners. STUDY DESIGN: Controlled laboratory study. METHODS: Twenty high-arched and 20 low-arched recreational runners (>10 miles per week) were recruited for the study. Three-dimensional kinematic and kinetics were collected as subjects ran at 3.5 ms(-1) +/- 5% along a 25-m runway. The motion control shoe evaluated was the New Balance 1122, and the cushioning shoe evaluated was the New Balance 1022. Repeated-measures analyses of variance were used to determine if low- and high-arched runners responded differently to motion control and cushion trainer shoes. RESULTS: A significant interaction was observed in the instantaneous loading rate such that the low-arched runners had a lower instantaneous loading rate in the motion control condition, and the high-arched runners had a lower instantaneous loading rate in the cushion trainer condition. Significant main effects for shoe were observed for peak positive tibial acceleration, peak-to-peak tibial acceleration, mean loading rate, peak eversion, and eversion excursion. CONCLUSION: These results suggest that motion control shoes control rearfoot motion better than do cushion trainer shoes. In addition, cushion trainer shoes attenuate shock better than motion control shoes do. However, with the exception of instantaneous loading rate, these benefits do not differ between arch type. CLINICAL RELEVANCE: Running footwear recommendations should be based on an individual's running mechanics. If a mechanical analysis is not available, footwear recommendations can be based empirically on the individual's arch type.

Adolescent↗

The effect of wearing the complete Lenox Hill Derotation Brace on energy expenditure during horizontal treadmill running at 161 meters per minute.

Ten volunteer subjects (means age = 26.6 +/- 4.9 years, means height = 177.9 +/- 5.6 cm, and means weight = 76.9 +/- 11.2 kg) who had been wearing the Lenox Hill Derotation Brace (LHB) for a mean time of 23.9 +/- 28.0 months were familiarized with horizontal treadmill running at 161 m/min with and without the LHB. They were then tested randomly for four runs, two with the LHB and two without the LHB. Metabolic measurements using a device that counted footstrikes on the treadmill were taken during the 3rd and 6th minutes of each run. Regardless of sampling time, wearing the LHB produced significantly higher values for VO2 (4.58%, P less than 0.025) and heart rate (5.10%, P less than 0.004) compared to the no brace condition. Regardless of whether or not the subjects were wearing the LHB, 6 minute values were significantly higher than 3 minute values for VO2 (5.89%, P less than 0.0004), VE (10.8%, P less than 0.004), heart rate (5.35%, P less than 0.0000), and R (2.17%, P less than 0.038). The mean 6 minute values of VO2 with (37.42 +/- 3.55 ml/kg/min) and without (35.54 +/- 2.17 ml/kg/min) the brace fall within the range of expected values of 28.1 to 39.3 ml/kg/min derived from regression equations from the literature which predict VO2 response to horizontal treadmill running. Mean stride lengths while wearing the LHB (97.85 cm) were not significantly different from mean stride lengths without the LHB (98.56 cm). It is concluded that wearing the LHB produces a 4.58% increase in energy expenditure during horizontal treadmill running at 161 m/min which cannot be attributed to changes in stride length or to time of sampling during the run.

Adult↗

Physiologic responses to maximal treadmill and deep water running in men and women.

Maximal physiologic responses to treadmill running and deep water running using a flotation device were compared in 12 trained men and 12 trained women. Although the men had significantly higher ventilation volumes, VO2max (liters of oxygen per minute and milliliters of oxygen per kilogram per minute), there were no significant differences in maximal heart rates or respiratory exchange ratios between the sexes. Significantly lower ventilation volumes, VO2max (LO2.min-1 and mlO2.kg-1.min-1), and heart rates were obtained in response to maximal water running compared to treadmill running, regardless of gender. Neither the men's nor women's maximal respiratory exchange ratios were significantly different between modes. The analysis of variance indicated that there were no significant interactions for any of the maximal responses to the tests between the sexes. The magnitude of these differences is similar to that found between treadmill running and cycling ergometry and should not preclude deep water running as a training technique. Caution, however, is advised if the training intensity is to be prescribed on the basis of land-determined heart rates.

Adult↗

Prevention of running injuries by warm-up, cool-down, and stretching exercises.

The purpose of this study was to evaluate the effect of a health education intervention on running injuries. The intervention consisted of information on, and the subsequent performance of, standardized warm-up, cool-down, and stretching exercises. Four hundred twenty-one male recreational runners were matched for age, weekly running distance, and general knowledge of preventing sports injuries. They were randomly split into an intervention and a control group: 167 control and 159 intervention subjects participated throughout the study. During the 16-week study, both groups kept a daily diary on their running distance and time, and reported all injuries. In addition, the intervention group was asked to note compliance with the standardized program. At the end of the study period, knowledge and attitude were again measured. There were 23 injuries in the control group and 26 in the intervention group. Injury incidence for control and intervention subjects was 4.9 and 5.5 running injuries per 1000 hours, respectively. The intervention was not effective in reducing the number of running injuries; it proved significantly effective (P < 0.05) in improving specific knowledge of warm-up and cool-down techniques in the intervention group. This positive change can perhaps be regarded as a first step on the way to a change of behavior, which may eventually lead to a reduction of running injuries.

Adult↗

Influence of photoperiod and running wheel access on the entrainment of split circadian rhythms in hamsters.

BACKGROUND: In the laboratory, behavioral and physiological states of nocturnal rodents alternate, with a period near 24 h, between those appropriate for the night (e.g., elevated wheel-running activity and high melatonin secretion) and for the day (e.g., rest and low melatonin secretion). Under appropriate 24 h light:dark:light:dark conditions, however, rodents may be readily induced to express bimodal rest/activity cycles that reflect a global temporal reorganization of the central neural pacemaker in the hypothalamus. We examine here how the relative length of the light and dark phases of the environmental cycle influences this rhythm splitting and the necessity of a running wheel for expression of this entrainment condition. RESULTS: Rhythm splitting was observed in wheel-running and general locomotion of Siberian and Syrian hamsters. The latter also manifest split rhythms in body temperature. Access to a running wheel was necessary neither for the induction nor maintenance of this entrainment pattern. While rhythms were only transiently split in many animals with two 5 h nights, the incidence of splitting was greater with twice daily nights of shorter duration. Removal of running wheels altered the body temperature rhythm but did not eliminate its clear bimodality. CONCLUSION: The expression of entrained, split circadian rhythms exhibits no strict dependence on access to a running wheel, but can be facilitated by manipulation of ambient lighting conditions. These circadian entrainment patterns may be of therapeutic value to human shift-workers and others facing chronobiological challenges.

Animals↗

Swing-leg retraction: a simple control model for stable running.

In running, the spring-like axial behavior of stance limbs is a well-known and remarkably general feature. Here we consider how the rotational behavior of limbs affects running stability. It is commonly observed that running animals retract their limbs just prior to ground contact, moving each foot rearward towards the ground. In this study, we employ a conservative spring-mass model to test the effects of swing-leg retraction on running stability. A feed-forward control scheme is applied where the swing-leg is retracted at constant angular velocity throughout the second half of the swing phase. The control scheme allows the spring-mass system to automatically adapt the angle of attack in response to disturbances in forward speed and stance-limb stiffness. Using a return map to investigate system stability, we propose an optimal swing-leg retraction model for the stabilization of flight phase apex height. The results of this study indicate that swing-leg retraction significantly improves the stability of spring-mass running, suggesting that swing-phase limb dynamics may play an important role in the stabilization of running animals.

Animals↗

Ankle plantar flexor force production is an important determinant of the preferred walk-to-run transition speed.

The mechanisms that govern the voluntary transition from walking to running as walking speed increases in human gait are not well understood. The objective of this study was to examine the hypothesis that plantar flexor muscle force production is greatly impaired at the preferred transition speed (PTS) due to intrinsic muscle properties and, thus, serves as a determinant for the walk-to-run transition. The plantar flexors have been shown to be important contributors to satisfying the mechanical energetic demands of walking and are the primary contributors to the observed ground reaction forces (GRFs) during the propulsion phase. Thus, if the plantar flexor force production begins to diminish near the PTS despite an increase in muscle activation, then a corresponding decrease in the GRFs during the propulsion phase would be expected. This expectation was supported. Both the peak anterior/posterior and vertical GRFs decreased during the propulsion phase at walking speeds near the PTS. A similar decrease was not observed during the braking phase. Further analysis using forward dynamics simulations of walking at increasing speeds and running at the PTS revealed that all lower extremity muscle forces increased with walking speed, except the ankle plantar flexors. Despite an increase in muscle activation with walking speed, the gastrocnemius muscle force decreased with increasing speed, and the soleus force decreased for walking speeds exceeding 80% PTS. These decreases in force production were attributed to the intrinsic force-length-velocity properties of muscle. In addition, the running simulation analysis revealed that the plantar flexor forces nearly doubled for similar activation levels when the gait switched to a run at the PTS due to improved contractile conditions. These results suggest the plantar flexors may serve as an important determinant for the walk-to-run transition and highlight the important role intrinsic muscle properties play in determining the specific neuromotor strategies used in human locomotion.

Adult↗

Spiders on a treadmill: influence of running activity on metabolic rates in Pardosa lugubris (Araneae, Lycosidae) and Marpissa muscosa (Araneae, Salticidae).

The CO2 release of the well-tracheated jumping spider, Marpissa muscosa, and the poorly tracheated, Pardosa lugubris, was tested while animals were running on a treadmill at three different speeds and under a selective elimination of lungs or tracheae. Thus, the influence of a well-developed tracheal system on the metabolism during physical exercise was examined. The CO2 release in intact animals increased with the running speed in both species. The costs of transport (COT) running at the maximal sustainable speed were nearly twice as big in M. muscosa as in P. lugubris. Elimination of one lung by sealing resulted in reduced COT and running times, and increasing anaerobic proportions in metabolism. Effects were greater in P. lugubris than in M. muscosa, indicating that tracheae compensate partly for the lacking lung capacity. Sealing of the tracheae in M. muscosa reduced the COT and the running times only at the highest speed. Results indicate that tracheae in M. muscosa support the aerobic metabolism only at the most intense physical exercise. At low and medium activity, tracheae may play their main role in the local supply of organs that are not involved in running activity.

Analysis of Variance↗

Sources of mechanical power for uphill running in humans.

During uphill running limb muscles must perform net mechanical work to increase the body's potential energy, while during level running the net mechanical work required is negligible as long as speed is constant. The increased demands for work as running incline increases might be met by an increase in power output at all joints, or only a subset of joints. We used inverse dynamics to determine which joints modulate net work output in humans running uphill. We measured joint kinematics and ground reaction force during moderate speed running at 0 degrees , 6 degrees and 12 degrees inclines. Muscle force, joint power and work per step were determined at the ankle, knee and hip using inverse dynamics calculations. We found that virtually all of the increase in work output with increasing incline resulted from increases in net work done at the hip (-0.25+/-0.23 J kg(-1), level, vs 0.88+/-0.10 J kg(-1), 12 degrees incline), while the knee and ankle performed similar functions at all inclines. The increase in work output at the hip resulted primarily from a large increase in average net muscle moment during stance (2.07+/-17.84 Nm, level, vs 87.30+/-13.89 Nm, 12 degrees incline); joint excursion increased by only 20% (41.22+/-3.41 degrees , level, vs 49.22+/-2.35 degrees , 12 degrees incline). The increase in hip muscle moment and power was associated with a poorer mechanical advantage for producing force against the ground. The increase in hip moment with running incline allows for the production of the power necessary to lift the body. This power may be developed by hip extensors or by transfer of power from muscles at other joints via biarticular muscles.

Adult↗