Literature DB >> 1893980

Functionally complex muscles of the cat hindlimb. III. Differential activation within biceps femoris during postural perturbations.

C M Chanaud1, J M Macpherson.   

Abstract

The biceps femoris (BF) muscle is divided into three neuromuscular compartments defined by the innervation patterns of the main nerve branches (English and Weeks 1987). The goals of this study were i) to determine how different regions of the biceps femoris muscle are activated in the intact cat during a broad range of limb movements evoked by perturbations of stance posture, and ii) to determine the relationship between the anatomical compartments of biceps femoris and the functional units as defined in this task. Cats were trained to stand on a moveable platform with each paw on a triaxial force plate. The animal's stance was perturbed by linear translation of the platform in each of sixteen different directions in the horizontal plane. EMG activity was recorded from eight sites across the width of the left biceps femoris muscle. During quiet stance only the anterior compartment was tonically active, presumably contributing to hip extensor torque in the maintenance of stance. During platform translation, evoked EMG activity was recorded from each electrode pair for a wide range of directions of perturbation; as direction changed progressively, the amplitude of evoked activity from any electrode pair increased to a maximum and then decreased. When the EMG amplitude was plotted in polar coordinates as a function of translation direction, the region of response formed a petal shaped area in the horizontal plane, termed the EMG tuning curve. The compartments of the BF muscle were not activated homogeneously. The tuning curve of the anterior BF compartment was similar to that of other hip extensors, and coincided with the region of postero-lateral force production by the hindlimb against the support. The tuning curve of the middle BF compartment was shifted in a counterclockwise direction from that of the anterior compartment, but overlapped extensively with it; the middle BF tuning curve was similar to that of anterior gracilis. The tuning curve of the posterior biceps compartment was rotated further counterclockwise and overlapped very little with that of the middle BF compartment. The posterior BF was activated in a pattern similar to that of other knee flexors. The functional units of BF activation were not identical with the neuromuscular compartments defined by the main nerve branches. As direction of the perturbation changed, the region of BF that was activated moved progressively across the muscle. This progression of the active region was continuous across BFa and BFm, whereas there was a jump, or discontinuity at the border between BFm and BFp.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1893980     DOI: 10.1007/bf00229406

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  19 in total

1.  Integrative pattern of Ia synaptic actions on motoneurones of hip and knee muscles.

Authors:  R M ECCLES; A LUNDBERG
Journal:  J Physiol       Date:  1958-12-04       Impact factor: 5.182

2.  Small, triaxial force plate.

Authors:  D W Lywood; D J Adams; A van Eyken; J M Macpherson
Journal:  Med Biol Eng Comput       Date:  1987-11       Impact factor: 2.602

3.  Robotic force platform for the study of posture and stance in the quadruped.

Authors:  A van Eyken; S Perlin; D W Lywood; J M Macpherson
Journal:  Med Biol Eng Comput       Date:  1987-11       Impact factor: 2.602

4.  Strategies that simplify the control of quadrupedal stance. I. Forces at the ground.

Authors:  J M Macpherson
Journal:  J Neurophysiol       Date:  1988-07       Impact factor: 2.714

5.  An electromyographic analysis of muscular activity in the hindlimb of the cat during unrestrained locomotion.

Authors:  I Engberg; A Lundberg
Journal:  Acta Physiol Scand       Date:  1969-04

6.  Automatic postural responses in the cat: responses to headward and tailward translation.

Authors:  D S Rushmer; C J Russell; J macpherson; J O Phillips; D C Dunbar
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

7.  Cumulative sum technique and its application to the analysis of peristimulus time histograms.

Authors:  P H Ellaway
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1978-08

8.  Localization of monosynaptic Ia excitatory post-synaptic potentials in the motor nucleus of the cat biceps femoris muscle.

Authors:  B R Botterman; T M Hamm; R M Reinking; D G Stuart
Journal:  J Physiol       Date:  1983-05       Impact factor: 5.182

9.  Functionally complex muscles of the cat hindlimb. IV. Intramuscular distribution of movement command signals and cutaneous reflexes in broad, bifunctional thigh muscles.

Authors:  C A Pratt; C M Chanaud; G E Loeb
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

10.  The organization and development of compartmentalized innervation in rat extensor digitorum longus muscle.

Authors:  R J Balice-Gordon; W J Thompson
Journal:  J Physiol       Date:  1988-04       Impact factor: 5.182

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  24 in total

1.  Motor antagonism exposed by spatial segregation and timing of neurogenesis.

Authors:  Marco Tripodi; Anna E Stepien; Silvia Arber
Journal:  Nature       Date:  2011-10-19       Impact factor: 49.962

2.  Extraction of individual muscle mechanical action from endpoint force.

Authors:  Jason J Kutch; Arthur D Kuo; William Z Rymer
Journal:  J Neurophysiol       Date:  2010-04-14       Impact factor: 2.714

3.  Spatial EMG potential distribution of biceps brachii muscle during resistance training and detraining.

Authors:  Kohei Watanabe; Motoki Kouzaki; Toshio Moritani
Journal:  Eur J Appl Physiol       Date:  2015-08-09       Impact factor: 3.078

4.  Functionally complex muscles of the cat hindlimb. V. The roles of histochemical fiber-type regionalization and mechanical heterogeneity in differential muscle activation.

Authors:  C M Chanaud; C A Pratt; G E Loeb
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

5.  Electromyographic responses from the hindlimb muscles of the decerebrate cat to horizontal support surface perturbations.

Authors:  Claire F Honeycutt; Jinger S Gottschall; T Richard Nichols
Journal:  J Neurophysiol       Date:  2009-03-25       Impact factor: 2.714

6.  Functionally complex muscles of the cat hindlimb. I. Patterns of activation across sartorius.

Authors:  C A Pratt; G E Loeb
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

7.  The mechanical actions of muscles predict the direction of muscle activation during postural perturbations in the cat hindlimb.

Authors:  Claire F Honeycutt; T Richard Nichols
Journal:  J Neurophysiol       Date:  2013-12-04       Impact factor: 2.714

Review 8.  Motor unit recruitment for dynamic tasks: current understanding and future directions.

Authors:  Emma F Hodson-Tole; James M Wakeling
Journal:  J Comp Physiol B       Date:  2008-07-03       Impact factor: 2.200

Review 9.  Functional and architectural complexity within and between muscles: regional variation and intermuscular force transmission.

Authors:  Timothy E Higham; Andrew A Biewener
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-05-27       Impact factor: 6.237

10.  Estimation of musculoskeletal models from in situ measurements of muscle action in the rat hindlimb.

Authors:  Sang Hoon Yeo; Christopher H Mullens; Thomas G Sandercock; Dinesh K Pai; Matthew C Tresch
Journal:  J Exp Biol       Date:  2011-03-01       Impact factor: 3.312

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