Muscle Force Output and Electromyographic Activity in Squats With Various Unstable Surfaces

2013 ◽  
Vol 27 (1) ◽  
pp. 130-136 ◽  
Author(s):  
Atle H. Saeterbakken ◽  
Marius S. Fimland
1999 ◽  
Vol 159 (3) ◽  
pp. 892-895 ◽  
Author(s):  
SPYROS ZAKYNTHINOS ◽  
THEODOROS VASSILAKOPOULOS ◽  
ANTONIOS MAVROMMATIS ◽  
CHARIS ROUSSOS ◽  
GEORGE E. TZELEPIS

2019 ◽  
pp. 1-10 ◽  
Author(s):  
Paulo H. Marchetti ◽  
Marcelo M. S. Miyatake ◽  
Roberto A. Magalhaes ◽  
Willy A. Gomes ◽  
Josinaldo J. Da Silva ◽  
...  

1996 ◽  
Vol 75 (5) ◽  
pp. 2050-2070 ◽  
Author(s):  
S. J. Bonasera ◽  
T. R. Nichols

1. The stretch-evoked reflex organization of muscles whose major action is to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis posterior (TP); flexor digitorum longus (FDL); flexor hallucis longus (FHL)] the ankle, and their interactions with the hindlimb extensors gastrocnemius (G) and soleus (S), were studied in 27 unanesthetized decerebrate cats. Ramp-hold-release stretches of physiological amplitudes were applied to muscle tendons detached from their bony insertion, and muscle force output was measured in response to these perturbations. Flexion and crossed-extension reflexes were used to modulate baseline force. 2. PB and TP shared strong, length-dependent, short-latency inhibitory reflexes prominent when the muscles were either actively generating force or quiescent. The mechanical characteristics of this reflex suggest Ia reciprocal inhibition as the underlying mechanism. Just as reciprocal inhibition between S and tibialis anterior stiffens the ankle joint against sagittal perturbations, we propose that reciprocal inhibition between PB and TP stiffens the ankle joint against nonsagittal perturbations. 3. In all preparations (n = 7) and under all conditions examined, PB and PL shared well-demonstrated mutual excitation. The reflex responses were asymmetric (favoring excitation of PL), length dependent, and occurred simultaneously with the stretch reflex at a latency of 16-18 ms. Mutual monosynaptic projections previously described between these two muscles explain all of the above findings. Our data further demonstrate that, under certain conditions, the ensemble activity of this reflex interaction has a powerful effect on the mechanical behavior of the muscle. 4. The heterogenic reflex organization of the ankle adductors was as follows: FDL evoked a modest excitation on TP, whereas FHL evoked weak inhibition. Latency of the excitation from FDL onto TP (24 ms) was greater than expected if the reflex were mediated by heteronymous Ia afferents. In all preparations examined (n = 3), TP contributed no significant reflexes onto either FDL or FHL. 5. Mutual, asymmetric inhibition characterized interactions between PB and the plantarflexors S and G. Most remarkable was a novel, long-latency (72-74 ms) reflex inhibition evoked on both S and G by stretch of PB. When this inhibition occurred, it dramatically decreased the S (or G) stretch response. Longer PB lengths evoked greater inhibition of isometric S; regression analysis indicated that the model best predicting this inhibition contained muscle force and stiffness terms. No long-latency reflexes were noted from either G or S onto PB. The mechanism underlying long-latency inhibition is presently unknown; however, features of this interaction suggest interneurons receive either group II or group III afferent input. 6. G and TP shared short latency, mutually inhibitory, asymmetric reflexes favoring inhibition of TP. No long-latency interactions were noted, nor were there any mechanically significant interactions between S and TP. 7. Reflex interactions across the abduction/adduction axis thus favored inhibition of plantarflexion and adduction torques while emphasizing abduction torques: PB/S (or PB/G) interactions were mutual, asymmetric, and favored inhibition of G and S; TP/G interactions were mutual, asymmetric, and favored inhibition of TP; TP/PB interactions were approximately balanced. The overall mechanical outcome of these inhibitory interactions may partly underlie the global corrective strategy seen in intact cats subjected to linear perturbations. 8. No significant reflex interactions were demonstrated between PL and TP, G, or S, nor were any long-latency reflexes noted. Thus, whereas reflex interactions between the stereotypically activated PB and other stereotypically activated muscles (including TP, G, and S) were strong and well-demonstrated, interactions between the variably activated PL and these same muscles were far weaker.


1985 ◽  
Vol 54 (3) ◽  
pp. 565-577 ◽  
Author(s):  
G. E. Loeb ◽  
J. A. Hoffer

Chronically implanted electrodes and nerve cuff catheters were used to record the activity of individual muscle spindle afferents during treadmill walking as low doses of lidocaine were infused around the femoral nerve to progressively block gamma motoneuron activity. Both primary and secondary endings from both the monarticular knee extensors and the biarticular hip/knee muscles of the anterior thigh showed large decreases in afferent activity, usually well before changes in the electromyographic activity, force output, or length and velocity were seen in the parent muscles. This decline in the proprioceptive signal feeding back onto the spinal cord, which we presume to have involved most of the spindles supplied by the femoral nerve, did not cause noticeable irregularities or instability of the walking gait. At the peak of the fusimotor blockade, spindle afferents from knee extensor muscles lost about half of their usually brisk activity during the near-isometric contraction of the stance phase. Significant decreases in the response to passive stretch during the flexion phase also occurred. At the peak of the fusimotor blockade, spindle afferents from the biarticular muscles lost all of their activity during the rapidly shortening swing phase and about half of their activity during the rapidly lengthening stance phase. For both monarticular and biarticular muscle spindles, the activity decreases in stance and swing phase often occurred at distinctly different stages of the progressive fusimotor blockade, indicating several different sources of fusimotor control. From these data, we infer that the sensitivity of most spindle afferents is substantially influenced by fusimotor activity during phases of both extrafusal activity and extrafusal silence. At least some of this influence appears to come from fusimotor neurons whose recruitment is independent of the extrafusal recruitment. The extent and type of fusimotor effects on spindle afferent sensitivity (dynamic or static) appear to be specialized for the mechanical events that tend to occur during those phases.


2011 ◽  
Vol 105 (5) ◽  
pp. 2169-2180 ◽  
Author(s):  
Xiaogang Hu ◽  
Karl M. Newell

This study investigated the interactive influence of organismic, environmental, and task constraints on the organization of redundant force coordination patterns and the hypothesis that each of the three categories of constraints is weighted based on their relative influence on coordination patterns and the realization of the task goal. In the bimanual isometric force experiment, the task constraint was manipulated via different coefficients imposed on the finger forces such that the weighted sum of the finger forces matched the target force. We examined three models of task constraints based on the criteria of task variance (minimum variance model) and efficiency of muscle force output (coefficient-independent and coefficient-dependent efficiency models). The environmental constraint was quantified by the perceived performance error, and the organismic constraint was quantified by the bilateral coupling effect (i.e., symmetric force production) between hands. The satisficing approach was used in the models to quantify the constraint weightings that reflect the interactive influence of different categories of constraints on force coordination. The findings showed that the coefficient-dependent efficiency model best predicted the redundant force coordination patterns across trials. However, the within-trial variability structure revealed that there was not a consistent coordination strategy in the online control of the individual trial. The experimental findings and model tests show that the force coordination patterns are adapted based on the principle of minimizing muscle force output that is coefficient dependent rather than on the principle of minimizing signal-dependent variance. Overall, the results support the proposition that redundant force coordination patterns are organized by the interactive influence of different categories of constraints.


1992 ◽  
Vol 2 (2) ◽  
pp. 47-55 ◽  
Author(s):  
Ira M. Fiebert ◽  
Jeannie M. Haas ◽  
Karen J. Dworkin ◽  
William G. LeBlanc

2016 ◽  
Vol 41 (10) ◽  
pp. 1052-1056 ◽  
Author(s):  
W.C. Ian Janes ◽  
Brandon B.G. Snow ◽  
Caisie E. Watkins ◽  
Elecia A.L. Noseworthy ◽  
Jonathan C. Reid ◽  
...  

Much of the static stretching (SS) literature reports performance impairments with prolonged SS. However, it has been acknowledged that a limitation of these studies is participants’ knowledge or bias. Since many participants have knowledge of the literature, their performance may be subconsciously influenced by expectations. Hence, the objective of this study was to examine the effect of stretching knowledge or deception on subsequent force output following SS. Two groups of male participants who were either aware (BIASED: 14) or unaware (DECEPTION: 14) of the SS literature participated. Unaware participants were misinformed that SS increases force production. Testing involved maximal voluntary isometric contractions (MVC) of the quadriceps and hamstrings at pre-, post-, and 5 min post-intervention (three 30-s passive hamstring stretches to the point of discomfort with 30-s rest intervals) or control. While the DECEPTION group displayed impaired knee flexion force (p = 0.04; 3.6% and 10.4%) following hamstrings SS, there was no significant impairment with the BIASED (–1.1% and +0.9%) group. Both groups exhibited hamstrings F200 (force produced in the first 200 ms) impairments following SS. Whereas BIASED participants exhibited an overall decrease (p < 0.05; 1.8% and 4.2%) in knee extension MVC, DECEPTION participants showed (p = 0.005; 8.8% and 5.1%) force increases. The quadriceps F200 was not significantly affected with the BIASED group but overall there were 4.5% and 8.7% F200 impairments at 1 and 5 min post-intervention (p = 0.05) with the DECEPTION group. Thus while deception resulted in enhanced quadriceps muscle force output, there was no knowledge or deception advantage when stretching the hamstrings.


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