Vastus medialis (VM) weakness is thought to alter patellar tracking, thereby changing the loading of the patellofemoral joint (PFJ), resulting in patellofemoral pain. However, it is challenging to measure VM force and weakness in human studies, nor is it possible to measure the associated mechanical changes in the PFJ. To obtain fundamental insight into VM weakness and its effects on PFJ mechanics, the authors determined PFJ loading in the presence of experimentally simulated VM weakness. Skeletally mature New Zealand White rabbits were used (n = 6), and the vastus lateralis, VM, and rectus femoris were stimulated individually through 3 custom-built nerve cuff electrodes. Muscle torque and PFJ pressure distribution were measured while activating all muscles simultaneously, or when the vastus lateralis and rectus femoris were activated, while VM was not, to simulate a quadriceps muscle strength imbalance. For a given muscular joint torque, peak pressures were greater and joint contact areas were smaller when simulating VM weakness compared with the condition where all muscles were activated simultaneously. The results in the rabbit model support that VM weakness results in altered PFJ loading, which may cause patellofemoral pain, often associated with a strength imbalance of the knee extensor muscle group.
Seong-won Han, Andrew Sawatsky, Azim Jinha and Walter Herzog
Tom G. Welter and Maarten F. Bobbert
We have investigated, in fast movements, the hypothesis that bi-articular muscles are preferentially selected to control me direction of force exerted on the environment, while mono-articular muscles are selected to control both this exerted force direction as well as the movement direction. Fourteen subjects performed ballistic arm movements involving shoulder and elbow rotations in the horizontal plane, either with or without an external force applied at the wrist. Joint torques required to counteract the external force were in the same order of magnitude as those required to overcome the inertial load during movements. EMG was recorded from mono- and bi-articular flexors and extensors of me elbow and shoulder. Signals were rectified and integrated (IREMG) over 100 ms following the first detected activity. MANOVA revealed mat, contrary to the hypothesis, IREMG of bi-articular muscles varied with movement direction just as that of the mono-articular muscles. It was concluded that the present data do not support me hypothesis mentioned above. A second finding was that movement effects on IREMG were much stronger than external force effects. This could not be explained using Hill's force-velocity relationship. It may be an indication that in the initiation of fast movements, IREMG is not only tuned to movement dynamics and muscle contractile properties, but also to me dynamics of the build up of an active state of the muscle.
Robert J. Neal and Barry D. Wilson
Three-dimensional kinematics and kinetics for a double pendulum model golf swing were determined for 6 subjects, who were filmed by two phase-locked Photosonics cameras. The film was digitally analyzed. Abdel-Aziz and Karara's (1971) algorithm was used to determine three-dimensional spatial coordinates for the segment endpoints. Linear kinematic and kinetic data showed similarities with previous studies. The orientation of the resultant joint force at the wrists was in the direction of motion of the club center of gravity for most of the downswing. Such an orientation of the force vector would tend to prevent wrist uncocking. Indeterminate peak angular velocities for rotations about the X axis were reported. However, these peaks were due to computational instabilities that occurred when the club was perpendicular to the YZ plane. Furthermore, the motion of the club during the downswing was found to be nonplanar. Wrist uncocking appeared to be associated with the resultant joint torque and not the resultant joint force at the wrists. Torques reported in this study were consistent with those reported by Vaughan (1981).
Yoann Blache, Maarten Bobbert, Sebastien Argaud, Benoit Pairot de Fontenay and Karine M. Monteil
In experiments investigating vertical squat jumping, the HAT segment is typically defined as a line drawn from the hip to some point proximally on the upper body (eg, the neck, the acromion), and the hip joint as the angle between this line and the upper legs (θUL-HAT). In reality, the hip joint is the angle between the pelvis and the upper legs (θUL-pelvis). This study aimed to estimate to what extent hip joint definition affects hip joint work in maximal squat jumping. Moreover, the initial pelvic tilt was manipulated to maximize the difference in hip joint work as a function of hip joint definition. Twenty-two male athletes performed maximum effort squat jumps in three different initial pelvic tilt conditions: backward (pelvisB), neutral (pelvisN), and forward (pelvisF). Hip joint work was calculated by integrating the hip net joint torque with respect to θUL-HAT (WUL-HAT) or with respect to θUL-pelvis (WUL-pelvis). θUL-HAT was greater than θUL-pelvis in all conditions. WUL-HAT overestimated WUL-pelvis by 33%, 39%, and 49% in conditions pelvisF, pelvisN, and pelvisB, respectively. It was concluded that θUL-pelvis should be measured when the mechanical output of hip extensor muscles is estimated.
Hans H.C.M. Savelberg, Ingrid G.L. Van de Port and Paul J.B. Willems
By manipulating trunk angle in ergometer cycling, we studied the effect of body configuration on muscle recruitment and joint kinematics. Changing trunk angle affects the length of muscles that span the hip joint. It is hypothesized that this affects the recruitment of the muscles directly involved, and as a consequence of affected joint torque distributions, also influences the recruitment of more distal muscles and the kinematics of distal joints. It was found that changing the trunk from an upright position to approximately 20 deg forward or backward affected muscle activation patterns and kinematics in the entire lower limb. The knee joint was the only joint not affected by manipulation of the lengths of hip joint muscles. Changes in trunk angle affected ankle and hip joint kinematics and the orientation of the thigh. A similar pattern has been demonstrated for muscle activity: Both the muscles that span the hip joint and those acting on the ankle joint were affected with respect to timing and amplitude of EMG. Moreover, it was found that the association between muscle activity and muscle length was adapted to manipulation of trunk angle. In all three conditions, most of the muscles that were considered displayed some eccentric activity. The ratio of eccentric to concentric activity changed with trunk angle. The present study showed that trunk angle influences muscle recruitment and (inter)muscular dynamics in the entire limb. As this will have consequences for the efficiency of cycling, body configuration should be a factor in bicycle design.
Elena J. Caruthers, Julie A. Thompson, Ajit M.W. Chaudhari, Laura C. Schmitt, Thomas M. Best, Katherine R. Saul and Robert A. Siston
Sit-to-stand transfer is a common task that is challenging for older adults and others with musculoskeletal impairments. Associated joint torques and muscle activations have been analyzed two-dimensionally, neglecting possible three-dimensional (3D) compensatory movements in those who struggle with sit-to-stand transfer. Furthermore, how muscles accelerate an individual up and off the chair remains unclear; such knowledge could inform rehabilitation strategies. We examined muscle forces, muscleinduced accelerations, and interlimb muscle force differences during sit-to-stand transfer in young, healthy adults. Dynamic simulations were created using a custom 3D musculoskeletal model; static optimization and induced acceleration analysis were used to determine muscle forces and their induced accelerations, respectively. The gluteus maximus generated the largest force (2009.07 ± 277.31 N) and was a main contributor to forward acceleration of the center of mass (COM) (0.62 ± 0.18 m/s2), while the quadriceps opposed it. The soleus was a main contributor to upward (2.56 ± 0.74 m/s2) and forward acceleration of the COM (0.62 ± 0.33 m/s2). Interlimb muscle force differences were observed, demonstrating lower limb symmetry cannot be assumed during this task, even in healthy adults. These findings establish a baseline from which deficits and compensatory strategies in relevant populations (eg, elderly, osteoarthritis) can be identified.
Eric J. Sprigings and Doris I. Miller
Optimized computer simulation, using a mathematical model of a diver, was employed to gain insight into the primary mechanical factors responsible for producing height and rotation in dives from the reverse group. The performance variable optimized was the total angular displacement of the diver as measured from last contact to the point where the diver's mass center passed the level of the springboard or platform. The times of onset, and lengths of activation for the joint torque actuators, were used as the control variables for the optimization process. The results of the platform simulation indicated that the magnitude of the hip torque was approximately twice that generated by the knee joint during the early extension phase of the takeoff. Most of the knee extension for the simulation model coincided with the period of reduced hip torque during the later phase of takeoff, suggesting that the knee torque served mainly to stabilize the lower limbs so that the force from the powerful hip extension could be delivered through to the platform. Maintaining a forward tilt of the lower legs (~50° from the horizontal) during hip and knee extension appeared to be paramount for successful reverse somersaults. Although the movement pattern exhibited by the springboard model was limited by the torque activation strategy employed, the results provided insight into the timing of knee extension. Peak knee extension torque was generated just prior to maximum springboard depression, allowing the diver's muscular efforts to be exerted against a stiffer board. It was also apparent that the diver must maintain an anatomically strong knee position (~140°) at maximum depression to resist the large upward force being exerted by the springboard against the diver's feet. The optimization process suggested that, as the number of reverse somersaults increases, both the angle of the lower legs with respect to the springboard and the angle of knee extension at completion of takeoff should decrease.
Original Research Validity and Reliability of Methods for Testing Vertical Jumping Performance Herbert Hatze * 5 1998 14 2 127 140 10.1123/jab.14.2.127 Research Relationship between Knee Joint Torque, Velocity, and Muscle Activation: Considerations for Musculoskeletal Modeling David Hawkins
* Gertjan Ettema * 2 2007 23 1 12 19 10.1123/jab.23.1.12 Musculotendon Parameters and Musculoskeletal Pathways Within the Human Foot Melissa R. Lachowitzer * Anne Ranes * Gary T. Yamaguchi * 2 2007 23 1 20 41 10.1123/jab.23.1.20 Effects of Upper Trunk Rotation on Shoulder Joint Torque among Baseball
1993 9 4 315 328 10.1123/jab.9.4.315 Book Reviews Book Reviews 11 1993 9 4 329 330 10.1123/jab.9.4.329 Research What Is a Joint Torque for Joints Spanned by Multiarticular Muscles? 11 1993 9 4 333 336 10.1123/jab.9.4.333 jab Journal of Applied Biomechanics 1065-8483 1543-2688 1993 9 4 10.1123/jab.1993