In vivo determination of triceps surae muscle?tendon complex viscoelastic properties

2004 ◽  
Vol 92 (4-5) ◽  
Author(s):  
Jan Babic ◽  
Jadran Lenarcic
Keyword(s):  
Viscoelastic Properties ◽  
Triceps Surae ◽  
Triceps Surae Muscle

scholarly journals Considerations on the human Achilles tendon moment arm for in vivo triceps surae muscle–tendon unit force estimates

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Denis Holzer ◽  
Florian Kurt Paternoster ◽  
Daniel Hahn ◽  
Tobias Siebert ◽  
Wolfgang Seiberl
Keyword(s):  
Achilles Tendon ◽  
Triceps Surae ◽  
Muscle Forces ◽  
Moment Arm ◽  
Unit Force ◽  
Plateau Region ◽  
Triceps Muscle ◽  
Triceps Surae Muscle ◽  
The Individual

Abstract Moment arm-angle functions (MA-a-functions) are commonly used to estimate in vivo muscle forces in humans. However, different MA-a-functions might not only influence the magnitude of the estimated muscle forces but also change the shape of the muscle’s estimated force-angle relationship (F-a-r). Therefore, we investigated the influence of different literature based Achilles tendon MA-a-functions on the triceps surae muscle–tendon unit F-a-r. The individual in vivo triceps torque–angle relationship was determined in 14 participants performing maximum voluntary fixed-end plantarflexion contractions from 18.3° ± 3.2° plantarflexion to 24.2° ± 5.1° dorsiflexion on a dynamometer. The resulting F-a-r were calculated using 15 literature-based in vivo Achilles tendon MA-a-functions. MA-a-functions affected the F-a-r shape and magnitude of estimated peak active triceps muscle–tendon unit force. Depending on the MA-a-function used, the triceps was solely operating on the ascending limb (n = 2), on the ascending limb and plateau region (n = 12), or on the ascending limb, plateau region and descending limb of the F-a-r (n = 1). According to our findings, the estimated triceps muscle–tendon unit forces and the shape of the F-a-r are highly dependent on the MA-a-function used. As these functions are affected by many variables, we recommend using individual Achilles tendon MA-a-functions, ideally accounting for contraction intensity-related changes in moment arm magnitude.

scholarly journals The effects of triceps surae muscle stimulation on localized achilles subtendon tissue displacements

2021 ◽  
Author(s):  
Nathan L. Lehr ◽  
William H. Clark ◽  
Michael D. Lewek ◽  
Jason R. Franz
Keyword(s):  
Achilles Tendon ◽  
Muscle Activation ◽  
Triceps Surae ◽  
Medial Gastrocnemius ◽  
Muscle Stimulation ◽  
Triceps Surae Muscle ◽  
Ankle Angle ◽  
In Series ◽  
Fixed End

The triceps surae muscle tendon unit is comprised of the lateral and medial gastrocnemius (MG) and soleus (SOL) muscles and three in series elastic “subtendons” that form the Achilles tendon. Comparative literature and our own in vivo evidence suggests that sliding between adjacent subtendons may facilitate independent muscle actuation. We aim to more clearly define the relation between individual muscle activation and subtendon tissue displacements. Here, during fixed-end contractions, electrical muscle stimulation controlled the magnitude of force transmitted via individual triceps surae muscles while ultrasound imaging recorded resultant subtendon tissue displacements. We hypothesized that MG and SOL stimulation would elicit larger displacements in their associated subtendon. 10 young adults completed 4 experimental activations at 3 ankle angles (-20°, 0°, 20°) with knee flexed to approximately 20°: MG stimulation (STIMMG), SOL stimulation (STIMSOL), combined stimulation, and volitional contraction. At 20° plantarflexion, STIMSOL elicited 49% larger tendon non-uniformity (SOL – MG subtendon tissue displacement) than that of STIMMG (p=0.004). For STIMSOL, a one-way post-hoc ANOVA revealed a significant main effect of ankle angle (p=0.009) on Achilles tendon non-uniformity. However, peak tendon non-uniformity decreased by an average of 61% from plantarflexion to dorsiflexion, likely due to an increase in passive tension. Our results suggest that localized tissue displacements within the Achilles tendon respond in anatomically consistent ways to differential patterns of triceps surae muscle activation, but these relations are highly susceptible to ankle angle. This in vivo evidence points to at least some mechanical independence in actuation between the human triceps surae muscle-subtendon units.

Morphological changes of the triceps surae muscle-tendon unit during passive extension: an in vivo rabbit model

1998 ◽  
Vol 13 (8) ◽  
pp. 634-640 ◽  
Author(s):  
Jui-Sheng Sun ◽  
Yi-Shiong Hang ◽  
Yang-Hwei Tsuang ◽  
Cheng-Kung Cheng ◽  
King-Yaw Tsao ◽  
...  
Keyword(s):  
Morphological Changes ◽  
Rabbit Model ◽  
Triceps Surae ◽  
Triceps Surae Muscle

scholarly journals Cyclooxygenase inhibition does not impact the pressor response during static or dynamic mechanoreflex activation in healthy decerebrate rats

2019 ◽  
Vol 317 (3) ◽  
pp. R369-R378 ◽  
Author(s):  
Korynne S. Rollins ◽  
Tyler D. Hopkins ◽  
Alec L. Butenas ◽  
Kennedy P. Felice ◽  
Carl J. Ade ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Pressor Response ◽  
Muscle Afferents ◽  
Triceps Surae ◽  
Prostaglandin E ◽  
Muscle Stretch ◽  
Triceps Surae Muscle ◽  
Cox Inhibitor

Passive limb movement and limb muscle stretch in humans and animals are common experimental strategies used to investigate activation of the muscle mechanoreflex independent of contraction-induced metabolite production. Cyclooxygenase (COX) metabolites, however, are produced by skeletal muscle stretch in vitro and have been found to impact various models of mechanoreflex activation. Whether COX metabolites influence the decerebrate rat triceps surae muscle stretch mechanoreflex model remains unknown. We examined the effect of rat triceps surae muscle stretch on the interstitial concentration of the COX metabolite prostaglandin E2 (PGE2). Interstitial PGE2 concentration was increased above baseline values by 4 min of both static (38% increase, P = 0.01) and dynamic (56% increase, P < 0.01) triceps surae muscle stretch ( n = 10). The 4-min protocol was required to collect enough microdialysis fluid for PGE2 detection. The finding that skeletal muscle stretch in vivo was capable of producing COX metabolites prompted the hypothesis that intra-arterial administration of the COX inhibitor indomethacin (1 mg/kg) would reduce the pressor and cardioaccelerator responses evoked during 30 s (the duration most commonly used in the rat mechanoreflex model) of static and dynamic rat triceps surae muscle stretch. We found that indomethacin had no effect ( P > 0.05, n = 9) on the pressor or cardioaccelerator response during 30 s of either static or dynamic stretch. We conclude that, despite the possibility of increased COX metabolite concentration, COX metabolites do not activate or sensitize thin-fiber muscle afferents stimulated during 30 s of static or dynamic hindlimb skeletal muscle stretch in healthy rats.

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