Biomedical subjects

Sharon R Bullimore

Publications and source records attributed to Sharon R Bullimore.

5 recordsLinked to original sources

PubMed2006

History-dependence of isometric muscle force: effect of prior stretch or shortening amplitude.

It is well-recognised that steady-state isometric muscle force is decreased following active shortening (force depression, FD) and increased following active stretch (force enhancement, FE). It has also been demonstrated that passive muscle force is increased following active stretch (passive FE). Several studies have reported that FD increases with shortening amplitude and that FE and passive FE increase with stretch amplitude. Here, we investigate whether these trends continue with further increases in shortening or stretch amplitude. Experiments were performed using in situ cat soleus muscles (n=8 for FD; n=7 for FE and passive FE). FD, FE and passive FE were measured after shortening or stretch contractions that covered as wide a range of amplitudes as practically possible without damaging the muscles. FD increased approximately linearly with shortening amplitude, over the full range of amplitudes investigated. This is consistent with the hypothesis that FD arises from a stress-induced inhibition of crossbridges. FE increased with stretch amplitude only up to a point, and then levelled off. Passive FE, and the transient increase in force at the end of stretch, showed relationships to stretch amplitude that were qualitatively very similar to the relationship for FE, increasing only until the same critical stretch amplitude had been reached. We conclude that FE and passive FE do not increase with stretch amplitude under all circumstances. This finding has important consequences for determining the mechanisms underlying FE and passive FE because any mechanism that is proposed to explain them must be able to predict it.

Animals↗

PubMed2006

Dynamically similar locomotion in horses.

It is possible for animals of very different sizes to use the same patterns of locomotion, i.e. to move in a ;dynamically similar fashion'. This will only occur, however, if relevant biomechanical parameters scale with size in such a way that they compensate for the effects of size differences. Here we apply this principle to understanding the effects of size on locomotion within a species: the domestic horse. We predict that, without any factor to compensate for size differences, detectable deviations from dynamically similar locomotion would occur over the size range present in adult horses. We measured relative stride length (RSL) and duty factor (DF) in 21 trotting horses (body mass: 86-714 kg), and interpolated the data to predict RSL and DF at equivalent speeds (Froude numbers: 0.5, 0.75, 1.0). RSL and DF at equal Froude number were not significantly related to body mass. This is consistent with the hypothesis that horses trot in a dynamically similar fashion at equal Froude number. We show that the nonlinear stress-strain relationship of tendon can contribute to reducing deviations from dynamic similarity, ;buffering' the effects of variation in body mass, but conclude that this effect is unlikely to explain fully our results. This suggests that a ;compensatory distortion' may occur in horses, counteracting the effects of size differences. The approach used here is also applicable to understanding the consequences of size changes within an individual during growth.

Animals↗

PubMed2005

Consequences of forward translation of the point of force application for the mechanics of running.

In running humans, the point of force application between the foot and the ground moves forwards during the stance phase. Our aim was to determine the mechanical consequences of this 'point of force translation' (POFT). We modified the planar spring-mass model of locomotion to incorporate POFT, and then compared spring-mass simulations with and without POFT. We found that, if leg stiffness is adjusted appropriately, it is possible to maintain very similar values of peak vertical ground reaction force (GRF), stance time, contact length and vertical centre of mass displacement, whether or not POFT occurs. The leg stiffness required to achieve this increased as the distance of POFT increased. Peak horizontal GRF and mechanical work per step were lower when POFT occurred. The results indicate that the lack of POFT in the traditional spring-mass model should not prevent it from providing good predictions of peak vertical GRF, stance time, contact length and vertical centre of mass displacement in running humans, if an appropriate spring stiffness is used. However, the model can be expected to overestimate peak horizontal GRF and mechanical work per step. When POFT occurs, the spring stiffness in the traditional spring-mass model is not equivalent to leg stiffness. Therefore, caution should be exercised when using spring stiffness to understand how the musculoskeletal system adapts to different running conditions. This can explain the contradictory results in the literature regarding the effect of running speed on leg stiffness.

Acceleration↗

PubMed2005

Scaling of elastic energy storage in mammalian limb tendons: do small mammals really lose out?

It is widely believed that elastic energy storage is more important in the locomotion of larger mammals. This is based on: (a) comparison of kangaroos with the smaller kangaroo rat; and (b) calculations that predict that the capacity for elastic energy storage relative to body mass increases with size. Here we argue that: (i) data from kangaroos and kangaroo rats cannot be generalized to other mammals; (ii) the elastic energy storage capacity relative to body mass is not indicative of the importance of elastic energy to an animal; and (iii) the contribution of elastic energy to the mechanical work of locomotion will not increase as rapidly with size as the mass-specific energy storage capacity, because larger mammals must do relatively more mechanical work per stride. We predict how the ratio of elastic energy storage to mechanical work will change with size in quadrupedal mammals by combining empirical scaling relationships from the literature. The results suggest that the percentage contribution of elastic energy to the mechanical work of locomotion decreases with size, so that elastic energy is more important in the locomotion of smaller mammals. This now needs to be tested experimentally.

Animals↗

PubMed2004

Distorting limb design for dynamically similar locomotion.

Terrestrial mammals of different sizes tend to move in a dynamically similar manner when travelling at speeds corresponding to equal values of the Froude number. This means that certain dimensionless locomotor parameters, including peak vertical ground reaction force relative to body weight, stride length relative to leg length and duty factor, are independent of animal size. The Froude number is consequently used to define equivalent speeds for mammals of different sizes. However, most musculoskeletal-tissue properties, including tendon elastic modulus, do not scale in a dynamically similar manner. Therefore, mammals could not be completely dynamically similar, even if perfectly geometrically similar. We argue that, for mammals to move in a dynamically similar manner, they must exhibit systematic 'distortions' of limb structure with size that compensate for the size independence of the tendon elastic modulus. An implication of this is that comparing mammals at equal Froude numbers cannot remove all size-dependent effects. We show that the previously published allometry of limb moment arms is sufficient to compensate for size-independent tendon properties. This suggests that it is an important factor in allowing mammals of different sizes to move in a dynamically similar manner.

Animals↗