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Engineering, 2012, 5, 99-102 doi:10.4236/eng.2012.410B025 Published Online October 2012 (http://www.SciRP.org/journal/eng) Copyright © 2012 SciRes. ENG Motor Imagery did not Improve Strength of Biceps Brachii* Lanxiang H e , Zhijun Tian College of Health S cience, Wu han Sports U niversity, Wuhan, China Email: he-lanxiang@126.com Received 2012 ABSTRACT Numerous studies have confirmed that motor imagery may result in plastic change in motor system as actual physical activity. How- ever, whether motor imagery can improve muscle strength of the trained persons remains unclear. The aim of this study is to investi- gate the effect o f motor imagery o n muscle stren gth. Total ly 12 healthy college stu dents were in volved in 4 weeks of mental rehear- sal of right upper limb movements (flexion and extension of elbow) during 30 min supervision session three times a week. Electro- myogram (EMG) and peak torque of biceps brachii, reaction time of subjects were analyzed. Results showed that no significant change in EMG of biceps br achii was observed during motor imagery. After motor rehearsal for 4 weeks, statistically significant difference i n E MG, p eak to rqu e and reacti vity were n o t ob ser ved (P > 0.05) when compared with the baseline data. Therefore, motor imagery co ul d no t enhan ce muscl e st ren gth o f sub ject s. Whet her ment al p ractice i s a valid reh ab ili tatio n t echniqu e n eeds to be in ve s- tigated further. Keywords: Moto r Imager y; EMG; Peak Tor que; R eaction Time 1. Introduction Motor imagery is a mental process of a movement without any overt movement or without any muscle activation[1-2]. The effects of motor imagery on motor learning and motor recovery have been investigated extensively for many years. Numerous studies have indicated that motor imagery may enhance motor recovery and motor learning, which have many aspects in common. One of possible mechanisms is that motor imagery can result in the activation of motor cortex in brain, which is the same as actual physical activity. However, it is still disputed whether motor imagery can improve motor rehabilitation. Es- pecially, whether motor imagery can enhance muscle strength is still unclear. In this study, 12 healthy college students were recruited for participating motor imagery of upper limb movement (elbow flexion and extension). The physiological parameters including reaction time, EMG and peak torque of biceps brachii were recorded and analyzed after 4 weeks of motor imagery. This study aims to investigate whether motor imagery can increase muscle strength of participants, which may be helpful for per- sons with sport injury to improve their muscle strength or delay their muscle atrophy. 2. Participants and Protocol 2.1. Participants Totally 12 healthy college students (6 females and 6 males, 21-24 years old) volunteered to participate in this study. During the study, all participants did not perform any physical exercise. 2.2. Protocol At the 1st week of trial, baseline data of EMG, muscle strength, and reaction time were collected. Then the participants were instructed to perform motor imagery of right elbow flexion and extension according to the protocol. At the 2nd week of trial, the participants started to perform daily motor imagery for 30 min, three times per week for four consecuti ve weeks. During motor imagery process, EMG of biceps brachii was also recorded. At the 6th week of trial, their muscle strength, EMG and r eaction time of right biceps were detected agai n. 3. Methods and Instruments 3.1. Messurement of Muscle Strength Participants were seated in a chair. Their right arm was semi- flexed and was mounted during all measurements. Strength of biceps brachii was measured concentrically at 60° per second on an isokinetic dynamometer (Biodex-4, USA). The peak tor- que (Newton meters, N-m) was recorded and stored on a per- sonal computer for offline analysis. 3.2. Messurement of Reaction Time The reaction time was recorded by reaction time detector (FYS-I, China). The red light signals were given from the front of the subject. The subject pressed the button using his right hand while responding to the red signal. The mean value of three measurements was used fo r analysis. 3.3. Messurement of EMG Electromyograph (ME6000T16, Finland)was used for col- lecting EMG data. The surface electrodes attached to the skin over biceps brachii. The skin was cleaned for the adherence of the electrodes and detection of EMG. The raw EMG signals were band-pass filtered (10-500 Hz) and recorded. The data were collected at 1000 Hz and analyzed with Mega-Win soft- *This research was supported by Wuhan Sports University. L. X. HE, Z. J. TIAN Copyright © 2012 SciRes. ENG 100 ware. 3.4. Data Analysis The mean power frequency (MPF) and root mean square (RMS) were calculated from the observed EMG. RMS was used as an indicator of the total myoelectric activity. The MPF served to indicate the firing rate of motor units as it is linearly related to the action potential conduction velocity of the muscle fibre[3]. The Student t-test for paired samples ( measures before trial and after trial) was applied using SPSS (version 13.0). The significant difference was considered at the P value less than 5%. 4. Results EMG signals of biceps brachii was detected motionless situa- tion (Figure 1A), motor imagery (Figure 1B), isometric con- traction (Figure 1C), and isotonic contraction (Figure 1D), respectively. EMG activity in motionless situation and motor imagery both were in baseline level. As shown in Table 1, surface EMG activity of biceps br achii did not change signifi- cantly after motor imagery for 4 weeks (P > 0.05). It suggested that, EMG activity of biceps brachii did not exhibit a significant change due to motor imagery of elbow flexion. Strength of biceps brachii was also measured concentrically at 60° per second on an isokinetic dynamometer. The peak torque of biceps brachii after motor imagery was bigger than that before motor imagery. The reaction time after motor im- agery was shorter than that before motor imagery. As shown in Table 1, no significant difference was achieved (P > 0.05). 5. Discussion Learning a motion skill is just to establish a motion conditioned reflex, which includes sensory input, signals integration by brain cortex and signals output to effectors (muscle). The im- provement o f th ese factors may b e in favor of learning a motion skill. (A.motionless B. motor imagery C. isometri c contracti on D. isotoni c contracti on) Figure 1. Electromyogram of Bicipital Muscle of Right a rm. Table 1. Reaction Time, Surfac e EMG and Peak Torque of Biceps Brachii (Mean±SD). Surface EMG P eak Torque (N.m) Reaction Time (s) RMS (μV) MPF ( Hz ) Before Trial 442.1±187.9 63.2±6.1 33.57±12.74 0.3567±0.0425 After Trial 429. 7±169.6 67.0±9.5 35.82±12.70 0.3299±0.0291 P >0.05 >0.05 >0.05 >0.05 L. X. HE, Z. J. TIAN Copyright © 2012 SciRes. E NG 101 Brain functional representations and their connections have plasticity [4]. Repeat motion training can stimulate or excite its brain functional representations and strengthen their connec- tions each other, which will be of benefit to sport performance. Motor imagery is a mental activity. It is a dynamic state dur- ing which the representation of a specific motor action is inter- nally activated without any motor output. Increasing evidences have confirmed that both motor imagery and actual physical activity can activate cortical motor areas in the central nervou s system. Therefore, the effect of motor imagery on learning motion skill and motor recovery from sport injury has gained tremendous attention. Previous reports have demonstrated that mental practice can increase i ts accu rac y thro ugh ping-pong ball tossing experiment, which suggests that motor imagery may be a useful tool in learning a new motor skill[5]. However, for learning the abduc- tion of the big toe, only subjects who had some experience in the task improved significantly after mental practice as well as after ph ysical p ractic e[ 6] . For patien ts, mot or r ecover y is a kin d of relearning of motor skill actually. Motor imagery has been also proved to be helpful for motor recovery of patients with stroke[ 7]. Mechanism of motor imagery is less well understood. Cur- rently, two hypotheses are used for the explanation of motor imagery[8-9]. The central mechanism has made an assumption that motor imagery can stimulate the same cortical areas as actual physical activity and strengthen the connections of rela- tive functional representations, which is supported by function- al magnetic r es onan ce imaging (fMRI). The activation in dorsal premotor cortex, superior parietal lobe and intraparietal sulcus is observed and the cortical repre- sentati ons are over lapped partially during the motor imagery of the participants [10]. Imagery of right-hand finger movements can induce a cortical activation pattern including dorsal and ventral portions of the premotor cortex, frontal medial wall areas, and cortical areas lining the intraparietal sulcus in both cerebral hemispheres[11]. Motor imagery not only has similar functions of neural networks as real physical activity [12], but also can modulate corticomotor excitability[13]. However, a novel continuous pointing method was used to measure and precisely characterize self-motion perception dur- ing actual movement and imagined movement through space. The results have revealed that the spatial updating processes that o ccur during actual self-motion were not evidenced during imagined movement [14]. The peripheral mechanism has supposed that motor imagery may result i n neural impulse o utput so th at myoelectrical acti v- ity may increase and more fibers may contract synchronously, thus improving muscle strength [15-17] According to Fontani’s report, 30 male participants with motor imagery (karate) have achieved same results in muscle strength improvement as actual training group. However, no obviou s change in reacti vity is n ot observed in mental imagery group[16]. Similarly, 11 stroke patients subjected to motor imagery training have greatly improved their limb functions [16]. In contrast, 39 stroke patients involved in mental practice for 4 weeks have revealed inconsistent results [18]. In our study, healthy college students involved in mental practice for 4 weeks also d id not exhibit a significant ch ange in surface EMG signal and peak torque when compared with the data before trial, which suggested that 4 weeks of motor imagery training is not enough to enhance muscle strength. Muscle strength is highly correlated with neural system func- tions such as modulating velocity and frequency of neural im- pulse. Faster neural impulse from motor cortex to arm muscles can lead to shorter reaction time. In the present study, motor imagery did not result in the decrease of reaction time, thus suggestin g that mental practice has no effect on th e modulation of neural impulse velocity. This result is consistent with Fon- tani’s report[16]. In a word, extensive investigations have demonstrated that motor imagery can stimulate cortical functional areas, and the rehabilitation of patients with dyskinesia may benefit from motor imagery [19]. However, the improvement of muscle strength through motor imagery is still lack of convincing evi- dences. The motor imagery (elbow flexion) for 4 weeks can not improve the strength of biceps in right arm. The optimal train- ing protocol should be further explored in the future. 6. Acknowledgements We are very grateful to Dr. Ning Chen for helpful comments and revi s e. REFERENCES [1] T. Mulder. “Motor imagery and action observation: cognitive tools for rehabilition,” J Neural Transm, vol.114(10), pp.1265-1278, 2007. [2] M. Lotze, L.G. Cohen, “Volition and imagery in neurorehabili- tion,” Cogn Behav Neurol, vol.19(3), pp.135-140, 2006. [3] A. Lucía, J. Hoyos, J.L. Chicharro, “The slow component of VO2 in professional cyclists,” Br J Sports Med, vol.34, pp.367-374, 2000. [4] M. Fiori, M. Tinazzi, S.M. Aglioti, “Selective impairment of hand mental rotation in patients with focal hand dystonia,” Brain, vol.129(1) , pp.47-54, 2006. [5] J.R. 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