Figures
Abstract
Purpose
Given the co-existence of post-activation potentiation (PAP) and fatigue within muscle, it is not known whether PAP could influence performance and pacing during distance running by moderating fatigue. The aim of this study was to assess the influence of PAP on pacing, jumping and other physiological measures during a self-paced 30 km trial.
Methods
Eleven male endurance-trained runners (half-marathon runners) volunteered to participate in this study. Runners participated in a multi-stage 30 km trial. Before the trial started, determination of baseline blood lactate (bLa) and countermovement jump (CMJ) height was performed. The self-paced 30 km trial consisted of 6 × 5 km splits. At the end of each 5 km split (60 s break), data on time to complete the split, CMJ height, Rating of Perceived Exertion (RPE) and blood lactate were collected while heart rate was continuously monitored.
Results
There was a significant decrease in speed (e.g. positive pacing strategy after the 4th split, p<0.05) with a progressive increase in RPE throughout the trial. Compared with baseline, CMJ height was significantly (p<0.05) greater than baseline and was maintained until the end of the trial with an increase after the 5th split, concomitant with a significant reduction in speed and an increase in RPE. Significant correlations were found between ΔCMJ and ΔSPEED (r = 0.77 to 0.87, p<0.05) at different time points as well as between RPE and speed (r = -0.61 to -0.82, p<0.05).
Conclusion
Our results indicates that fatigue and potentiation co-exist during long lasting endurance events, and that the observed increase in jump performance towards the end of the trial could be reflecting a greater potentiation potentially perhaps counteracting the effects of fatigue and preventing further reductions in speed.
Citation: Del Rosso S, Barros E, Tonello L, Oliveira-Silva I, Behm DG, Foster C, et al. (2016) Can Pacing Be Regulated by Post-Activation Potentiation? Insights from a Self-Paced 30 km Trial in Half-Marathon Runners. PLoS ONE 11(3): e0150679. https://doi.org/10.1371/journal.pone.0150679
Editor: Maria Francesca Piacentini, University of Rome, ITALY
Received: December 5, 2015; Accepted: February 16, 2016; Published: March 2, 2016
Copyright: © 2016 Del Rosso et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All Excel files are available from Open Science Framework database (https://osf.io/rfy9t/).
Funding: The authors received a donation from Nova Biomedical (http://www.novabiomedical.com) for lactate analyses. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Nova Biomedical (http://www.novabiomedical.com) donated lactate analyzers to DAB. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Introduction
Performance in endurance events is the result of an athlete’s ability to achieve and maintain power output or speed over the course of a competition. This is achieved through strategies aimed at managing the rate of fatigue development and thus the reduction in speed which would be detrimental for performance [1, 2]. Consequently, ‘pacing strategy’ is the self-selected tactic used by athletes from the beginning of an event to distribute their work rate throughout the competition [1, 3, 4] in order to prevent premature fatigue and thus optimize performance [4, 5].
Pacing can be influenced by a number of factors, which can influence fatigue development and impair performance. In long-distance efforts (e.g. > 40 min) it has been suggested that pacing may be regulated by the perception of effort (often measured with Rating of Perceived Exertion [RPE] scales) where athletes adjust their running speed by comparing moment-to-moment the actual with the expected RPE for a given distance [6–8]. Several models have been proposed to explain fatigue in endurance sports [9]. Yet, it is known that the magnitude and etiology of fatigue would depend on the exercise under consideration and it has been recommended that the study of muscle fatigue should address both the perceived effort and the decline in force that occurs during sustained activity [10]. The main focus to explain how fatigue could influence pacing in endurance sports has been on centrally mediated mechanisms [3, 6, 11, 12]. However, the study of factors that integrate both peripheral and central fatigue with pacing strategies should also be of interest to better characterize endurance running events. This is important in light of evidence showing that group III/IV muscle afferents are involved in the development of both peripheral and central fatigue [13, 14]. Accordingly, it would be pertinent to consider that pacing could be regulated by mechanisms acting both at central and peripheral levels.
It has been pointed out that central fatigue alone cannot explain the entire muscle strength loss during and after prolonged running exercises [15] and that alterations at the neuromuscular level may also be involved. One potential factor relating fatigue and pacing could be the neuromuscular profile of the athletes. Since the classical work of Paavolainen and co-workers [16] it has been known that improving athlete’s muscle power through strength training improves endurance performance [17, 18]. More recently, Boullosa et al., [19] showed that, after a fatiguing running test, endurance-trained runners experienced an improvement in countermovement jump (CMJ) that correlated with an increase in peak power and a lower eccentric maximum strength loss during the CMJ. This finding was consistent with that reported by others [20] and it is believed to be associated with the co-existence of post-activation potentiation (PAP) and fatigue within the muscle. PAP is defined as an acute improvement of muscular performance characteristics as a result of the contractile history [21] and it has been suggested that the PAP response after running is specific for endurance-trained athletes [19, 22]. The most important mechanism that has been proposed in literature to explain PAP is phosphorylation of myosin regulatory light chains, which increases Ca2+ sensitivity of the myofilaments [23]. Alternatively, acute changes in muscle architecture and increased recruitment of higher order motor units have been also proposed as potential mechanisms [21]. It appears that PAP has its greatest effect during submaximal contractions in which motor units are firing at relatively low frequencies, such as the case of endurance exercise [24]. Furthermore, it could be argued that PAP might counteract the onset of fatigue [24] at the peripheral level. In addition, given that submaximal fatigue is defined as the balance between fatigue-induced impairments and neuromuscular strategies to sustain performance [25], it is possible that other mechanisms may play a role. Among these mechanisms, those acting to facilitate muscle performance are likely to be of importance. At a supraspinal level, neural potentiation could be one of those factors facilitating the maintenance of muscle performance during prolonged activities, as it has been suggested that ongoing contractions facilitate motoneuron excitation and contributes to improved force production [25]. However, while the acute effect of PAP in endurance athletes after different running exercises has been reported [26, 27], it is not known whether or not PAP would influence performance and pacing during endurance activities.
After a 30 km trial in endurance trained runners, Millet and co-workers [28] observed a ~23.5% reduction in maximal voluntary contraction of the knee extensors concomitant with a decrease in voluntary activation, which was attributed to central fatigue. Additionally, they found no change in low frequency fatigue and suggested that exercise may have potentiated the contraction torque and hidden the low frequency fatigue. As previously mentioned, the contractile history of a muscle contributes to both fatigue and potentiation [29] and it has been pointed out that potentiation can occur after both maximal and submaximal efforts in endurance trained athletes [19, 26, 27, 30]. Moreover, a comparison of endurance and power trained athletes showed that submaximal exercise can offset fatigue in endurance but not in power athletes [31]. This important difference could be partially attributed to the increase in the content of fast myosin light chains in slow-twitch fibers in endurance trained subjects, an adaptation that likely increases the capacity of myosin light chain phosphorylation. Accordingly, despite the ongoing increase in central fatigue and the reduced muscle activation through central mechanisms, the potentiation effect could be of importance for long distance runners to maintain or prevent further reductions in pacing.
Accordingly, the main purpose of this study was to assess the pacing adopted by a group of endurance-trained runners during a self-paced 30 km trial, along with perceived exertion, jump capacity, lactate, and HR responses to evaluate whether these responses, and more specifically the expected jump potentiation, might influence pacing.
Materials and Methods
Participants
Eleven male trained endurance athletes (half-marathon runners) volunteered to participate in this study (Table 1). For an expected effect size of 0.5 (moderate effect) and a minimum of 6 measurements for most of the variables, a sample of 8 participants would yield a statistical power of 0.95. All runners had at least five years of experience and were in the middle of their training macrocycle. The runners were training a mean of 8.6 ± 0.4 sessions and ~152.6 ± 3.9 km (133 to 172 km) per week with a volume per training session ranging from 8 to 25 km. Before engaging in any test, participants were informed about the risks and benefits of the study and provided written informed consent. The protocol of the study was approved by the Ethics Committee of Catholic University of Brasilia.
Procedures
Runners were required to participate in two separate testing sessions. The first was devoted to anthropometric measurements [i.e., percentage of body fat (%BF)], the assessment of maximum aerobic speed (MAS) and familiarization with the CMJ protocol. During the second session, a self-paced 30 km trial was carried out which consisted of 6 × 5 km splits on a course within the University campus. This uncommon competitive distance was selected to avoid the possible influence of competitive experience on running performance. Based on a previous study [32], a multi-stage approach was applied for evaluating the evolution of neuromuscular performance through the whole trial. At the end of each 5 km split, data on CMJ height, RPE (6–20 scale [33]) and blood lactate (bLA) were collected. In the case of RPE, the participants were instructed to report the effort perception for the entire previous split (i.e., akin to session RPE). In addition, heart rate (HR) and speed were monitored. The sessions were separated by 48–72 h to avoid the effects of residual fatigue (Fig 1). The order of the start when various athletes were evaluated in the same day was based on the individual MAS previously measured (i.e., the fastest runner was the first to start the trial) and subsequent runners started the 30 km trial every 5 min to avoid the effect of having a “rabbit” on performance [34]. However, it is worth noting that although faster athletes never surpassed the slower ones, on some occasions they crossed each other along the course.
UMTT = Université of Montreal Track Test, CMJ = Countermovement Jump, RPE = rate of perceived exertion, bLA = blood lactate.
Université de Montréal Track Test
The UMTT was carried out on a 400 m synthetic track and its protocol is described elsewhere [35] but the pacing was set using a bicycle equipped with a speedometer [26]. Briefly, the test started with a running speed of 8 km·h−1 and increased in 1 km·h−1every 2 min. Participants were instructed to run behind the bicycle and to avoid drafting. The test was terminated when the participants could no longer follow the pacing and distance ≈ 3 m from the bicycle. Maximum aerobic speed (MAS) was defined as the speed achieved in the last completed 2 min stage with recording of the total final time (TUMTT). Before and immediately after completing the UMTT the participants performed three CMJs separated by at least 15 s, in order to familiarize with the jump protocol.
Countermovement Jump Height (CMJ)
CMJ was selected because is easy to perform and has been shown that it could be used to reflect the effect of PAP and fatigue in athletes [19]. CMJ was recorded using a contact platform connected to a digital timer through an interface (ChronoJump-BoscoSystem) [36, 37]. The flight time of each individual jump was recorded and converted automatically to jump height by the specific software that was connected to a personal computer [37]. In each CMJ, participants were encouraged to jump as high as possible with the arms in akimbo (both hands on the hips) position. The depth of each jump was freely chosen by the participants [19]. In addition, the athletes were instructed to maintain their knees extended during the landing phase.
Self-Paced 30-km Trial
For the 30 km-trial, a 5 km course was demarcated inside the university campus. A global position system (GPS) monitor (Garmin Forerunner 305, Garmin Ltd., Olathe, KS, USA) with an accuracy of 0.05 m·s−1 in steady conditions was used by a researcher to measure the course to be completed by the runners. Participants arrived at the location at 07:00 h and were equipped with a heart rate (HR) monitor (Polar RS800 CX, Polar Electro Oy, Finland). Then, after resting quietly for 15 min, a blood sample was obtained for determination of baseline blood lactate (bLa) using a dry chemistry analyzer (Lactate Plus, Nova Medical, Waltham MA, USA). Body mass (BM) was measured using an electronic scale (Filizola ID 500, São Paulo, Brasil). Following these procedures, a standard warm-up was carried out consisting of 5 min of jogging at a personally selected intensity, dynamic stretches and two CMJs. Then, participants performed two maximal CMJ separated by 15 s to assess baseline CMJ height. The self-paced 30 km trial started at ~ 07:30 h and consisted of 6 × 5 km splits. The participants were instructed to run the entire course (i.e., 30 km) as fast as they can and were monitored by one researcher along the course. Each 5 km split started and finished at the same location. At the end of each split the runners stopped for measurements of bLA, RPE (6–20 scale [33]), and CMJ height (Fig 1). The order of the measurements was selected to minimize the time required to collect the data and was the following: split time, 1st CMJ, bLA and RPE, 2nd CMJ. The mean total time required for data collection at the end of each split was 60 s. In addition, HR was monitored continuously during the 30 km self-paced trial. The mean temperature and relative humidity during data collection was ~24.1°C and ~37.1%. During the trial, carbohydrate-electrolyte beverages (Gatorade®) were provided using labeled bottles for each participant and its consumption was allowed ad-libitum. Percentage dehydration was calculated as the difference between pre- and post-trial BW relative to pre-trial body mass. For each 5 km split, pacing was calculated as the percentage of speed variation of each split in relation to the mean speed for the 30 km (i.e., positive numbers implies that runners were faster than the mean speed and negative numbers implies that runners were slower than mean speed) [38]. ΔSPEED was calculated as the percentage of speed variation of each split in relation with the MAS (ΔSPEED = MAS—split speed), ΔCMJ was calculated as CMJ height registered at the end of each split minus the baseline height, and ΔCMJ% was defined as percentage of change in CMJ height in relation with baseline CMJ.
Statistical Analysis
Descriptive statistics were performed using mean, standard deviations and 95% confidence intervals. Normal distribution of the variables was assessed for each data point using the Shapiro-Wilk test and visual inspection of Q-Q plots. For those variables showing a non-normal distribution (e.g, lactate) a natural logarithmic transformation was used, meanwhile those variables showing a non-normal distribution in spite of transformation (i.e., PSE and HR), were assessed using non-parametric techniques (Mann-Whitney U Test for pairwise comparisons and Friedman Test for repeated measures). To assess the effects of time (i.e., stage: 5, 10, 15, 20, 25 and 30 km) an ANOVA for repeated measures was performed. Mauchly’s Sphericity was tested and if sphericity could not be assumed, then the Greenhouse-Geisser correction was used. For repeated measures, a Bonferroni post-hoc comparison was used to locate significant differences. Differences between the 1st and 2nd CMJ in each split were assessed using paired t tests. Also, the effect size for each condition was tested by Cohen’s d. Coefficient of variation (CV) was calculated for each variable at all 5 km splits and was averaged to obtain a mean for the sample. Pearson correlations were performed between different variables and such correlations were thereafter assessed for chances of a true effect using qualitative statistics [39] with the following thresholds: most unlikely, <0.5%; very unlikely, 0.5–5%; unlikely, 5–25%; possibly, 25–75%; likely, 75–95%; very likely, 95–99.5%; and most likely, >99.5%. All statistics were performed using IBM SPSS Statistics for Windows® (Version 20.0; Armonk, NY). The statistical significance was set at an alpha level of 0.05.
Results
The trial was completed in 118.5 ± 6.0 min with a mean speed of 3.87 ± 0.49 m·s−1 (15.2 ± 0.7 km·h−1). Table 2 shows the comparison of the different parameters obtained along the trial. Speed was constant from the start until a decrease was observed after the 4th split (p<0.001; ES = 0.6 to 2.2). The trend for pacing and speed expressed as %MAS was the same as for speed (p<0.001; ES = 0.7 to 1.5; Table 2). Additionally, speed expressed as a %MAS showed an increase at the end of the 2nd split (p<0.001; ES = 0.2). CMJ height increased from baseline (p<0.05, ES = 0.6 to 0.9) and thereafter it was maintained until the end of the trial. Interestingly, CMJ height increased in the 5th split and its value was significantly different from split 4th (p<0.05, ES = 0.2). There were no differences between the 1st and 2nd CMJ assessed within each split. RPE increased at the end of 4th split and reached the highest value at the end of the 6th split. HR increased significantly at the 2nd in comparison with the 1st split (p<0.05, ES = 0.6) and was maintained thereafter while HR expressed as a percentage of the HRmax showed no variation along the trial. Compared to baseline, bLa was higher until the 4th split (p<0.05, ES = 1.7 to 2.6) followed by a decrease at the 6th split, which was lower than the 4th split (p<0.05, ES = 0.7).
The mean body mass loss during the 30 km trial was 2.5 kg, representing a fluid loss of ~3.5%BM while fluid intake was 0.90 ± 0.3 L (0.3 to 1.6 L) yielding a carbohydrate intake of 53.8 ± 20.3 g (18.0 to 99.0 g).
Significant correlations were found between ΔCMJ at 10, 15, 20, 25 and 30 km and ΔSPEED at the 30 km (Fig 2). Qualitative analysis showed that chances of a true effect in these correlations ranged between very likely (98.7%) to most likely (99.9%). Other significant correlations between ΔCMJ and ΔSPEED were: ΔCMJ at 10 km vs ΔSPEED at 20 and 25 km (r = 0.63, p = 0.036 and r = 0.77, p = 0.006, respectively) and ΔCMJ at 15 km vs ΔSPEED at 20 and 25 km (r = 0.65, p = 0.029 and r = 0.77 p = 0.006, respectively). No other significant correlations were found between ΔCMJ and ΔSPEED for the rest of the splits. Also, significant and inverse correlations were found between RPE and speed (Table 3) at different splits and between MAS and ΔCMJ at 30 km (r = 0.77, p<0.05; Fig 3). Additionally, significant correlations were found between MAS and Speed at 15, 20, 25 km (r = 0.67 to 0.73, p<0.05).
An index that included both CMJ height and RPE score as CMJ/RPE was calculated and plotted this index vs. the speed along the trial. The natural logarithm of mean values in each stage for CMJ/RPE vs. speed showed a 3rd order fit (Fig 4; y = -1.5165x3 + 3.5764x2–2.4485x + 3.1776; r2 = 0.87).
Values are the natural logarithm of the mean for each split. The data was modeled with a 3rd order polynomial (y = -1.5165x3 + 3.5764x2–2.4485x + 3.1776; r2 = 0.875). The order of splits is reversed due to the logarithmic transformation; therefore the first split is the one on the farthest right.
Discussion
To the best of our knowledge this is the first study describing pacing and concurrent fatigue and potentiation during a self-paced 30 km trial run in endurance athletes. The main findings were: a decrease in speed and thus in pacing from the 4th split until the end of the trial, concomitant with an increase in CMJ from baseline followed by a maintenance of the jump performance; and the relationships between jump potentiation and speed decrements over the running trial. In addition, cardiovascular responses did not change during the trial while the metabolic responses showed a decline (i.e., ~53% in bLa levels) towards the end of the 30 km. Furthermore, RPE scores did not change until the end of the 20 km split. These results of a progressive decline in speed and increase in RPE throughout the trial are in line with previous studies [7, 8]. On the other hand, the increase and maintenance of CMJ height along the trial appears to be related to a potentiation effect as described earlier in endurance athletes [19, 20]
In long distance running, it has been suggested that pacing is regulated by the sensation of fatigue, where RPE acts to evaluate the perception of exertion during exercise [4, 8, 40]. It would appear that athletes adjust their running speed by comparing moment-to-moment the actual with the desirable RPE for a given distance [6, 8] based on an exercise template in the brain that is updated by previous experience and regulates exercise intensity. Our findings support such a contention given that the speed reduction observed in our runners coincided with the increase in RPE (Table 2). Furthermore, there is evidence that pacing is influenced by internal (e.g., glycogen levels) and external (e.g., environmental conditions, previous experience and competitions) cues [41]. In the present study, we observed an increase in bLA during the first splits and a decrease towards the end of the trial (Table 2). In this sense; being that carbohydrate availability appears to be critical in long-term events (> 90 min) [7], it is possible that speed reduction and RPE increases could be related to mechanisms associated with glycogen depletion (not monitored in the present study). It is worth noting that in our study participants had a fluid consumption of 0.90 ± 0.3 L (0.3 to 1.6 L) yielding a carbohydrate intake of 53.8 ± 20.3 g (18.0 to 99.0 g) during the entire trial. Also, there were no correlations between carbohydrate intake and the different measured variables. Recently, Gonzalez et al., [42] showed that carbohydrate ingestion did not prevent muscle glycogen depletion during prolonged cycling (3 h-bouts, 50% of peak power output). In fact, carbohydrate intake in the study of Gonzalez et al., [42] (1.7 g·min−1) was larger than the observed in our study (~0.45 g·min−1). Thus, it is likely that carbohydrate intake in our study had no substantial effect on muscle glycogen levels. Thus, the classic results from Karlsson and Saltin [43] of different pacing patterns in glycogen loaded vs. not loaded 30 km racers, argues in favor of the decrease in speed being attributable to the depletion of muscle glycogen.
While the previous rationale could partially explain the pacing regulation throughout the trial, it would not explain the increase in CMJ performance observed after the first 10 km and the subsequent maintenance of the jump potentiation (Table 2). In other words, despite the clear evidence of fatigue (decreased speed, elevated RPE), PAP was present throughout the trial. As previously noted, the study of muscle fatigue should address both the perceived effort and decline in force that occurs during sustained activity [10]. In this context, it has been shown that improving the neuromuscular characteristics of endurance athletes would lead to an improvement in performance. In fact, Damasceno et al., [44] observed that improvement in neuromuscular characteristics (i.e., half squat maximum dynamic strength and drop jump height) in recreational long distance runners were accompanied by a faster end-spurt and improvement of performance for the same RPE during a 10 km running time trial. These authors suggested that a possible explanation for the enhanced performance could be a higher motor unit synchronization that might result in strength potentiation and thus delay the onset of signals related to fatigue. In this context, it has been shown that endurance athletes can exhibit concurrent fatigue and potentiation [19, 20]. Moreover, as skeletal muscles can respond to homeostatic disturbances by initiating a facilitatory response to maintain force output [25] it is also possible that neural potentiation from both supraspinal and afferent input could contribute to the maintenance of force production. It can be argued that the threshold to recruit motor units is reduced with neural potentiation and thus fast twitch motor units might be easier to recruit allowing the improvement or maintenance of muscle performance (i.e., jump height and running speed) [25, 45]. Thus, our finding of an increase of CMJ performance could be reflecting a mechanism by which potentiation counteracts fatigue during prolonged exercise. Another appealing candidate for further examination is what has been termed a “peripheral governor” in skeletal muscle [46]. Recently, Froyd et al., [30] assessed potentiation and fatigue during an isokinetic knee extension/flexion time trial and found a significant correlation between indices of fatigue (i.e., post-exercise peak torque) and potentiation (i.e., post-exercise peak torque/pre-exercise peak torque), which would suggest that the same biological mechanisms that cause potentiation (changes in Ca2+ sensitivity) may also explain the development and recovery of peripheral fatigue. Thus, based on these previous findings and our results, it could be possible to suggest that pacing may be regulated at both central and peripheral level.
In line with the previous discussion, we found correlations between ΔCMJ at 10, 15, 20, 25 and 30 km and ΔSPEED at 30 km (Fig 2) meaning that those who exhibited the greater improvement in jumping performance (i.e., potentiation) also showed the greatest decrease in speed during the last split. While this could argue against our hypothesis that PAP moderates the effect of fatigue this also could be related to the fact that those running at higher intensities are more likely to exhibit potentiation [29] but in time are more prone to express muscular fatigue. The correlations between MAS and ΔCMJ at 6th split (Fig 3) and between MAS and Speed at 3rd, 4th and 5th split (r = 0.67 to 0.73, p<0.05) support this contention. Previously, Vuorimaa et al., [20] found a significant correlation between the enhancement of neuromuscular parameters during fatigue state and MAS in elite long distance runners which is consistent with our finding. More recently, Mettler and Griffin [47] have shown that muscular endurance did not change the pattern of motor unit firing rates but increased endurance time during a fatiguing task. As a partial explanation, the authors [47] suggested that endurance training allowed the central nervous system to sustain similar firing rates of motor units over a longer period of time. In this context, our data shows a clear breaking point after the 4th split (20 km), with a decrease in speed concomitant with an increase in CMJ height and RPE values (Table 2). In this sense, after a 30 km trial, Millet et al., [28] showed that subjects with the greatest knee extensors strength loss also experienced a large activation deficit, which was related with central fatigue. Additionally Millet et al [28] did not find changes in low frequency fatigue after a 30 km running trial and suggested that exercise may have potentiated the contraction torque and hidden the low frequency fatigue. Therefore, taking into account the current and previous findings, we may suggest that the observed increases in jumping performance through the trial may reflect a potentiation effect counterbalancing the effects of fatigue.
We also found an inverse correlation between RPE and speed at different splits (see Table 3). Previously, Crewe et al., [48] reported that the rise in RPE accurately predicted the duration of fixed-intensity exercises and suggested that the brain must be able to forecast the duration of exercise and then set the rate of increase in RPE. This appears to be true for our athletes as some correlations were observed between RPE at 5 km and speeds at 15–25 km, although it has been noticed that pace regulation based on effort perception can result in slower speeds with findings showing that altering perceptions of pace control have an impact on runners’ focus of attention [49]. On one hand these results could be related to the involvement of afferent information [14] as it has been noted that stimulation of III/IV muscle afferents contributes to the prevention of peripheral fatigue during exercise [13]. However, it has also been noticed that afferent feedback does not contribute significantly to perception of effort during exercise and other mechanisms, such as centrally generated forwarding neural signals, may be involved [50]. On the other hand, given that maximal voluntary muscle activation is considered a key indicator of central fatigue, our results of a maintained and increased jumping performance could suggest that PAP is acting to maintain muscle performance. This is in agreement with the results of a previous study [51] showing that endurance-trained athletes can maintain or increase vertical jump performance despite the fatigue induced by an interval training protocol through the improvement of mechanical variables via PAP. Consequently, considering all factors, it is tempting to suggest that in spite of the increase in RPE, the observed increase in CMJ height could be reflecting a peripheral mechanism counteracting the imbalance between fatigue and potentiation and thus a further loss in speed (i.e., greater than the observed decrease). In other words, the neuromuscular system must balance conflicting facilitatory and inhibitory responses in maintaining submaximal forces [25].
Based on the premise that, on one hand maintenance or increased jump performance would be associated with an increase or maintenance of speed and, on the other hand the elevated RPE due to fatigue would be related to a decrease in speed, we calculated an index that included both CMJ height and RPE score as CMJ/RPE and plotted this index vs. the speed along the trial (Fig 4). Interestingly, the mean values in each stage for CMJ/RPE vs. speed showed a 3rd order fit (r2 = 0.87), which might imply that balance between fatigue and potentiation could be modulating pacing. Even more interesting is that the model would predict a tendency towards maintenance or reduced CMJ/RPE index, but with a concomitant increase in speed, which could be due to the balance between fatigue and potentiation.
Although this was a multi-stage trial, it is worth mentioning that this model could be considered valid [32] to assess muscle function and pacing during prolonged endurance exercise in a more ecological condition [52]. In activities lasting between 2 min to several hours it has been suggested that competitors typically employ a U-shaped pacing strategy pattern [4, 53] and recently, Hanley [54] showed that half-marathon runners exhibit a reverse-J pacing profile during competitions with some slight differences between men and women. This, in time is associated with the concept of planned pacing strategies that regulate performance [4, 54, 55]. In this sense, although we did not observe such patterns, it is important to note that in our study the athletes were only males and did not run in groups, whereas the selected distance (i.e., 30 km) was not a common competitive distance (e.g., marathon or half marathon). Thus, while we were not able to gather data with a high level of precision within the splits (i.e., GPS), an end-spurt during the terminal segment of the trial (e.g. last km) might be indicative of an increase in PAP as a countermeasure to fatigue with more studies needed. Moreover, Santos-Lozano et al., [38] reported that top runners were those with lower variability in their speed (i.e., CV). In agreement with this, we found a moderate correlation between the CV for speed and total time (r = 0.64, p = 0.035). Therefore it seems that variability of pacing is an issue to consider when analyzing data from prolonged running.
Finally, given that it is known that fluid loss could influence performance during prolonged events [56] in warm environments, we monitored the hydration status by accounting for fluid ingestion and changes in body mass during the trial. The mean body mass loss during the 30 km run was 2.5 kg representing a fluid loss of 3.5%, which is within the acceptable limits of dehydration [56]. Moreover, recently a meta-analysis by Savoie et al. [57] showed that vertical jumping ability is not altered by hypohydration but suggested that a water loss equivalent to ~3% BW may improve performance in BW-dependent tasks. We found that athletes had no significant differences on hypohydration levels and a covariance analysis using percentage of dehydration as a covariate did not show significant results. Thus, it is possible to assume that in our athletes hypohydration had little or no effects on jumping performance.
Conclusions
In conclusion, we found a reduction in speed and pacing in the final 10 km of a 30 km trial concomitant with the increase in RPE while jumping performance increased from baseline and was maintained thereafter. From our results, it could be suggested that pacing can be regulated by two different mechanisms—one acting as an integrative central center, as reflected in RPE scores, and other acting at a peripheral level whereby the potentiation response increases muscle performance. The 3rd order polynomial fit of the CMJ/RPE index vs. Speed, could be representative of the balance between fatigue and potentiation showing a dual control of the pacing.
Acknowledgments
We would like to thank Nova Biomedical for their donation for lactate analyzers and the athletes for their enthusiastic participation.
Author Contributions
Conceived and designed the experiments: DAB ESB IOS LT. Performed the experiments: SDR ESB IOS LT. Analyzed the data: SDR ESB IOS. Contributed reagents/materials/analysis tools: DAB ESB IOS. Wrote the paper: SDR DGB CF DAB. Interpretation of the data: SDR DGB CF DAB. Revising the final draft: SDR ESB IOS LT DGB CF DAB.
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