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1.82 Volts 1 t T 2 m (t )dt T t RMS m(t) The Surface Mechanomyogram (MMG) 3.44 ms-2 f med 0 S m ( f ) df f med S m ( f ) df 406 μV 55 Nm I m(t ) t T t 0 1 m(t ) dt 2 3 seconds Mechanomyography (MMG) Non-invasive technique that records and quantifies the oscillations generated by dimensional changes of the active skeletal muscle fibers. Has also been called acoustic myography, phonomyography, sound myography, and vibromyography. “surface mechanomyogram” recommended at CIBA Foundation Symposium, 1995. Orizio, C. Critical Reviews in Biomedical Engineering. 1993. force sound water line muscle hydrophone When muscle fibers contract they oscillate or vibrate. Early MMG studies utilized isolated frog muscle in a sound-insulated chamber and recorded the oscillations with a hydrophone. Isometric muscle action at 30% MVC Displacement Sensor Accelerometer Laser Beam Bipolar EMG Electrodes Force Transducer Orizio, C., Gobbo, M., Diemont, B., Esposito, F., Veicsteinas, A. Eur J Appl Physiol. 2003. Watakabe, M., Itoh, Y., Mita, K., and Akataki, K. Med. Biol. Eng. Comput. 1998. During voluntary contractions, the oscillations create pressure waves that can be recorded at the skin’s surface using a crystal contact sensor or accelerometer. Over the years, there have been a number of hypotheses regarding the origin of the MMG signal that have been ruled out. Vascular sounds MMG can be recorded when blood flow is occluded. Friction between the microphone and skin MMG can be recorded in a water bath and with air coupled microphones. Friction between fascia and muscles Less MMG activity is recorded over fascia such as the vastus lateralis. No MMG activity during passive muscle actions. Bone oscillations MMG can be recorded from isolated muscle. Nerve conduction Ambient temperature does not affect MMG frequency, but does affect nerve conduction velocity. The MMG signal has three components: 1. 2. 3. A gross lateral movement at the initiation of a contraction generated by a non-simultaneous activation of muscle fibers. Smaller subsequent lateral oscillations at the resonant frequency of the muscle. Dimensional changes of the active fibers. Smith, D.B., Housh, T.J., Johnson, G.O., Evetovich, T.K., Ebersole, K.T., Perry, S.R. Muscle Nerve. 1998. The MMG signal is affected by many factors: Muscle temperature Stiffness Mass Intramuscular pressure Viscosity of the intracellular and extracellular fluid mediums Perry, S.R., Housh, T.J., Weir, J.P., Johnson, G.O., Bull, A.J., Ebersole, K.T. J. Electromyogr. Kinesiol. 2001. The MMG signal is low frequency: Typically bandpass filtered at 5-100 Hz, while EMG is 10-500 Hz. Time and frequency domains of the MMG signals have been used to examine various aspects of muscle function including: Neuromuscular fatigue Electromechanical delay Motor control strategies Muscle fiber type distribution patterns Diagnose neuromuscular disorders in adult and pediatric populations Low back pain Control external prostheses Effectiveness of anesthesia Although we are continually learning more, our knowledge of the MMG signal is probably 20-25 years behind that of the EMG signal. M. Stokes: “As knowledge of muscle sounds increases and the development of more appropriate methodology occurs, the potential uses and limitations of [MMG] must be reassessed continually.” We have examined the MMG signal in the time and frequency domains under a number of conditions in an attempt to both develop and test hypotheses. Isometric muscle actions Concentric muscle actions Eccentric muscle actions Passive movements Cross-talk Stretching interventions Resistance training interventions Isometric and Isokinetic Force vs. MMG and EMG amplitude and frequency relationships Coburn, J.W., Housh, T.J., Cramer, J.T., Weir, J.P., Miller, J.M., Beck, T.W., Malek, M.H., and G.O. Johnson. Electromyogr clin Neurophysiol. 2004. Increase in torque due only to increased recruitment of ST fibers – no change in frequency Torque increase is due to increased motor unit firing rate and not recruitment at > 80% MVC since MMG amplitude decreases. Increased frequency due to recruitment of FT fibers at > 50% MVC; these fibers have greater frequency than ST fibers Subjects: 1.0 Muscle actions: .9 Normalized MMG rms and MPF n = 10 (7 male, 3 female). .8 Leg extension: Isometric = 45° Isokinetic = 30°∙s-1 .7 .6 Torque: .5 .4 10 – 100% MVC. Parameters: .3 .2 .1 MMG amplitude and frequency. Muscles: 0.0 0 10 20 30 40 50 60 70 Percent Maximal Torque 80 90 100 Vastus medialis. Coburn, J.W., Housh, T.J., Cramer, J.T., Weir, J.P., Miller, J.M., Beck, T.W., Malek, M.H., & Johnson, G.O. (2004). J Strength Cond Res. in press. Subjects: n = 7 men Muscle actions: Leg extension: Isometric = 45° Isokinetic = 30°∙s-1 Torque: 20 – 100% MVC. Parameters: MMG & EMG amplitude and frequency. Muscles: Vastus medialis. Coburn, J.W., Housh, T.J., Cramer, J.T., Weir, J.P., Miller, J.M., Beck, T.W., Malek, M.H., & Johnson, G.O. (2004). J Strength Cond Res. in press. Subjects: n = 7 men Muscle actions: Leg extension: Isometric = 45° Isokinetic = 30°∙s-1 Torque: 20 – 100% MVC. Parameters: MMG & EMG amplitude and frequency. Muscles: Vastus Medialis Vastus medialis. Orizio, C., Gobbo, M., Diemont, B., Esposito, F., A. Veicsteinas. Eur J Appl Physiol. 2003. Biceps Brachii Assignments Complete all the normalization and graphing for our experimental data. Randomly assign the 5 articles posted on the website tonight Give a presentation on your article next week. PPT, 10 min, 5-min Q & A Discuss the results of your article and how they relate to our study. Mid-term exam/lab write-up (take home) due Monday after spring break (March 21).