We expected landings and drop jumps to produce significantly different muscle pre-activity. As far as the height factor is concerned, significant difference in muscle pre-activity was expected to exist between 40 cm and 60 cm, and 60 cm and 80 cm, in majority of the lower extremity muscles. Generally speaking, different types of deep jumps were characterized by significant difference in AmaxEMG between landings and drop jumps for majority of lower extremity muscles. Highest rebound was achieved from 60 cm platform, which was an optimal drop height for this group of subjects. Statistically significant differences in muscle pre-activity for 40 cm and 80 cm platforms compared to the pre-activity from the optimal drop height (60 cm) were observed only for EMG variables of a few muscles and not for the majority of them as it was expected (Table 4). Therefore, muscle pre-activity was not statistically greater in magnitude for drop heights above the optimal, and was not statistically lesser in magnitude for drop heights beneath the optimal. Considerable effect of the height factor on the pre- activity level implies that the EMG variables changed systematically with the change in the platform height, whereas the effect of the DJ type factor showed that the change in pre-activity depended on the platform height. In addition, the presented results show that pre-activity modulation was muscle-specific (mechanical action and anatomical characteristics of muscles), as revealed in some previous studies as well (Santelo et al., 2001). It should be noted that the results were obtained from athletes who were not familiar with the described jumping techniques, and that athletes with previous experience might have produced different results. Regarding the DJ type factor, only BDJ stood out with its muscle pre- activity values which were significantly higher than those in CL and BL. This result was anticipated, given the requirements of the movement task. BDJ requires amortization of impact force, followed by quick and explosive take off, which calls for stiff contractile component enabling utilization of elastic energy stored in the muscle-tendon complex (Finni et al., 2000; Kawakami et al., 2001). It is indicative of the fact that a certain amount of the generated pre-activity in BDJ should be used in performing the take-off. To determine whether such high pre-activity is related to creation of stable landing conditions or to subsequent reactive muscle activity, further studies are required. In these (BDJ) conditions, higher pre-activity is considered to be related (at least partly) to the take-off phase (not to the breaking phase), or otherwise, the same pre-activity would be achieved for BL, too. Hence, we cannot consider muscle pre-activity merely from the aspect of creating stable landing conditions. Movement characterized by longer phase of amortization before taking off (counter drop jump - CDJ) should be included in further studies. This type of DJ is more demanding in terms of coordination, from the aspect of the muscle force modulation (Bobbert et al., 1987; Bosco et al., 1982). It was assumed that in these conditions higher pre-activity would be used in the contact phase to absorb impact force and create stable conditions during braking phase. Patterns of muscle force development during CDJ should enable the performance of higher rebound, compared to BDJ. The results imply that AmaxEMG, as an indirect index of achieved muscle force (Santelo, 2005) is significantly higher for BDJ than for CL in the period before touchdown. This phenomenon was noticed in the majority of observed muscles. Unlike CL, the BL did not show any significant change in muscle pre-activity compared to BDJ. The first important conclusion was that BL was very similar to BDJ in reaching optimal muscle force during flight phase, i.e. in the moments just before the contact with the landing surface. Significantly higher activity of AmaxEMG for BDJ compared to BL was noticed only in activity of m.soleus (p = 0.022) and m.tibialis anterior (p = 0.042). High activity of m.tibialis anterior was necessary for building a co-activation mechanism. This mechanism creates a stiff system which provides stability of ankles in the initial stages of contact with the surface (Chimera et al., 2004; Kellis et al., 2003), which may have an adverse impact on take-offs. Earlier studies, however, showed that the activity of m.tibialis anterior changed under the influence of reciprocal inhibition (Kellis et al., 2003). Therefore, we can assume that this mechanism functions during the take-off. The measured values for m.tibialis anterior may also be influenced by the sample of subjects. The soccer players had not been exposed to these training methods prior to the study, and consequently they were not capable of performing adequate patterns of muscle activation, since the motor program had not been created (Kyrolainen and Komi, 1995, Viitasalo et al., 1998). The height factor proved to be most responsible for determining the pre-activity defined by AmaxEMG and iEMG. The results of this study confirmed the results of previous studies from the viewpoint that the muscle activity is well adjustable to the change in platform height, where increase in pre-activity followed the increase in platform height (Liebermann and Hoffman, 2005; Santelo et al., 1998; 2001). Change in muscles' electric activity was not the same for all muscles. Therefore, role of each muscle in the preparatory phase for landing should be analyzed separately. There appears to be a general strategy for adapting muscle force to the corresponding platform height, irrespective of anatomical structure and mechanic action of the lower extremity muscles (Santelo, 2005). Medial head of m.gastrocnemius showed inconsistency in adjusting electric activity to the height. Unlike the medial head, electromyographic response of lateral head showed higher sensitivity to changes of platform height. It was capable of finely adjusting the force of contractile component in pre-contact phase. Since the previous research showed that m.gastrocnemius medialis and m.gastrocnemius lateralis had a separate mechanical function (Wolf et al., 1998), we can conclude that they also have a distinct function in preparing lower leg for a specific movement. Indeed, this conclusion should be verified in future studies. Change of AmaxEMG with the increase in platform height was in accordance with the data obtained in previous studies (Santelo, 2005). Statistically significant differences were identified between the values for DJs from 40 cm and 80 cm (Kyrolainen and Komi, 1995; Liebermann and Hoffman, 2005). From the functional point of view, very large impact magnitudes in drops from 80 cm require high muscle force in order to prepare locomotor system for the contact with the surface. Accordingly, the intensity of deep jump trainings should increase gradually. This seems to be the only way to fine tune muscle activity in order to achieve the effects of the exercise. EMG amplitudes of m.tibialis anterior were observed to increase significantly for the 80 cm drop height, as compared to that of 40 cm and 60 cm (table 4). This is another indicator showing that DJ from 80 cm was rather demanding with respect to preparation of neuromuscular mechanism, causing high level of co-activation in these conditions (Kellis et al., 2003; Santelo et al., 2001). The significant decrease in the activity of m.gastrocnemius medialis for deep jumps from 80 cm, compared to 60 cm was detected for AmaxEMG (p = 0.029). The basic task for a subject during deep jumps from 80cm was to provide a level of muscle force which was sufficient to absorb the actual momentum on the contact with the surface. Significant decrease in pre-activity of m.gastrocnemius medialis might be explained to be a compensation for the increase in activity of other two plantar flexors - m.soleus and m.gastrocnemius lateralis. From the mechanical viewpoint, this mechanism was disadvantageous for performing the take-off, and advantageous for stable landing. When ankle is under pressure, all muscles behave synergically. Given that condition, it becomes irrelevant which of the heads has a dominant role. Capability of the CNS to anticipate the moment of landing is inversely proportional to the platform height. The ability to anticipate is not related only to the length of flight, but also to the momentum which a body has on contact with the ground (Santello and McDonagh, 1998). Both values (duration of the flying phase and the momentum which a body has at the moment of touchdown) correlate to the platform height (Santelo et al., 1998). Since the possibility of anticipating the moment of landing is smaller, the stabilization effects are provided by synergetic effect of the lower extremity muscles. Impossibility of anticipating is partly related to the timing of turning the motor units on, and mostly to unsystematic variability of muscle force gained just before the landing (Martin et al., 2002; Santelo et al., 2001). The above mechanism affected the ability to take off after landing from higher platforms, because the entire activity of extensors was used solely to perform the landing. Researchers have implied that many motor tasks are controlled by motor system generally (globally), rather than individually (locally) (Santelo, 2005). Under these circumstances, m.triceps surae did not have the ability to determine which of its heads had the stabilization role, and which one provided for the push-off phase. Since m.gastrocnemius medialis and m. gastrocnemius lateralis have independent mechanical functions (Wolf et al., 1998), it could be argued that m.gastrocnemius medialis and m.gastrocnemius lateralis functioned independently in preparation for landing, too. Pre-activity (iEMG) of m.soleus had a tendency to be sensitive to change from 40 cm to 60 cm (p = 0.072), whereas significant pre-activity difference was detected when height was changed from 40 cm and 80 cm (p = 0.005). In the semi-flexion phase, when it is necessary to perform explosive movement of the body from one position to another (such as cutting movements and deep jumps), anterior cruciate ligament is at the highest risk of being injured (Griffin et al., 2000; Hewett et al., 1999). M.soleus is agonistic (agonist) to anterior cruciate ligament, and it plays an important role in preventing injuries of passive knee structures (Elias et al., 2003). Increase of the platform height from 40 cm to 60 cm, and from 60 cm to 80 cm, resulted in an increase in body momentum which was likely to cause progressive disturbances in knee. In order to ensure the stiffness of the system, it is necessary to achieve high level of muscle force before landing, especially in the jumps from 80 cm. Considering the role of m.soleus in the stabilization of knee and ankle joints, its activity should mark high values, and most of this muscle's pre-activity might be used to prevent ligament injuries. |