scholarly journals Scaling of muscle fibres and locomotion

1992 ◽  
Vol 168 (1) ◽  
pp. 243-252 ◽  
Author(s):  
L. C. Rome
Keyword(s):  
Muscle Fibre ◽  
Body Mass ◽  
Fibre Type ◽  
Fibre Types ◽  
Energetic Cost ◽  
Muscle Fibres ◽  
Small Animals ◽  
Running Speed ◽  
Cost Of Locomotion ◽  
The Cost

To reconcile the scaling of the mechanics and energetics of locomotion to recent data on the scaling of the mechanics of muscle fibres, I have extended the theory of Taylor and colleagues that the energetic cost of locomotion is determined by the cost of generating force by the fibres. By assuming (1) that the cost of generating force in a fibre is proportional to V(max) (maximum velocity of shortening) and (2) that, at physiologically equivalent speeds, animals of different body sizes recruit the same fibre types, this extension quantitatively predicts the scaling of the energetics of locomotion, as well as other observations, from the scaling of V(max) of the muscle fibres. First, the energetic cost of locomotion at physiologically equivalent speeds scales with Mb-0.16, where Mb is body mass, as does V(max) of a given fibre type. However, the energetic cost at absolute speeds (cost of transport) scales with Mb-0.30, because small animals must compress their recruitment order into a narrower speed range and, hence, recruit faster muscle fibre types at a given running speed. Thus, it costs more for small animals to move 1 kg of their body mass 1 km not only because a given muscle fibre type from a small animal costs more to generate force than from a large one, but also because small animals recruit faster fibre types at a given absolute running speed. In addition, this analysis provides evidence that V(max) scales similarly to 1/tc (where tc is foot contact time) and muscle shortening velocity (V), in agreement with recent models. Finally, this extension predicts that, at physiologically equivalent speeds, the weight-specific energetic cost per step is independent of body size, as has been found empirically.

Speed, stride frequency and energy cost per stride: how do they change with body size and gait?

1988 ◽  
Vol 138 (1) ◽  
pp. 301-318 ◽  
Author(s):  
N. C. Heglund ◽  
C. R. Taylor
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Energy Cost ◽  
Reaction Force ◽  
Stride Frequency ◽  
Energetic Cost ◽  
Published Data ◽  
Frequency Change ◽  
Cost Of Locomotion ◽  
The Cost

In this study we investigate how speed and stride frequency change with body size. We use this information to define ‘equivalent speeds’ for animals of different size and to explore the factors underlying the six-fold difference in mass-specific energy cost of locomotion between mouse- and horse-sized animals at these speeds. Speeds and stride frequencies within a trot and a gallop were measured on a treadmill in 16 species of wild and domestic quadrupeds, ranging in body size from 30 g mice to 200 kg horses. We found that the minimum, preferred and maximum sustained speeds within a trot and a gallop all change in the same rather dramatic manner with body size, differing by nine-fold between mice and horses (i.e. all three speeds scale with about the 0.2 power of body mass). Although the absolute speeds differ greatly, the maximum sustainable speed was about 2.6-fold greater than the minimum within a trot, and 2.1-fold greater within a gallop. The frequencies used to sustain the equivalent speeds (with the exception of the minimum trotting speed) scale with about the same factor, the −0.15 power of body mass. Combining this speed and frequency data with previously published data on the energetic cost of locomotion, we find that the mass-specific energetic cost of locomotion is almost directly proportional to the stride frequency used to sustain a constant speed at all the equivalent speeds within a trot and a gallop, except for the minimum trotting speed (where it changes by a factor of two over the size range of animals studied). Thus the energy cost per kilogram per stride at five of the six equivalent speeds is about the same for all animals, independent of body size, but increases with speed: 5.0 J kg-1 stride-1 at the preferred trotting speed; 5.3 J kg-1 stride-1 at the trot-gallop transition speed; 7.5 J kg-1 stride-1 at the preferred galloping speed; and 9.4 J kg-1 stride-1 at the maximum sustained galloping speed. The cost of locomotion is determined primarily by the cost of activating muscles and of generating a unit of force for a unit of time. Our data show that both these costs increase directly with the stride frequency used at equivalent speeds by different-sized animals. The increase in cost per stride with muscles (necessitating higher muscle forces for the same ground reaction force) as stride length increases both in the trot and in the gallop.

Energetics of ascent: insects on inclines

1990 ◽  
Vol 149 (1) ◽  
pp. 307-317 ◽  
Author(s):  
R. J. Full ◽  
A. Tullis
Keyword(s):  
Oxygen Consumption ◽  
Minimum Cost ◽  
Metabolic Cost ◽  
Metabolic Energy ◽  
Stride Frequency ◽  
Energetic Cost ◽  
Incline Angle ◽  
Small Animals ◽  
Cost Of Locomotion ◽  
The Cost

Small animals use more metabolic energy per unit mass than large animals to run on a level surface. If the cost to lift one gram of mass one vertical meter is constant, small animals should require proportionally smaller increases in metabolic cost to run uphill. To test this hypothesis on very small animals possessing an exceptional capacity for ascending steep gradients, we measured the metabolic cost of locomotion in the cockroach, Periplaneta americana, running at angles of 0, 45 and 90 degrees to the horizontal. Resting oxygen consumption (VO2rest) was not affected by incline angle. Steady-state oxygen consumption (VO2ss) increased linearly with speed at all angles of ascent. The minimum cost of locomotion (the slope of the VO2ss versus speed function) increased with increasing angle of ascent. The minimum cost of locomotion on 45 and 90 degrees inclines was two and three times greater, respectively, than the cost during horizontal running. The cockroach's metabolic cost of ascent greatly exceeds that predicted from the hypothesis of a constant efficiency for vertical work. Variations in stride frequency and contact time cannot account for the high metabolic cost, because they were independent of incline angle. An increase in the metabolic cost or amount of force production may best explain the increase in metabolic cost. Small animals, such as P. americana, can easily scale vertical surfaces, but the energetic cost is considerable.

Moving cheaply: energetics of walking in the African elephant.

1995 ◽  
Vol 198 (3) ◽  
pp. 629-632 ◽  
Author(s):  
V A Langman ◽  
T J Roberts ◽  
J Black ◽  
G M Maloiy ◽  
N C Heglund ◽  
...  
Keyword(s):  
Fuel Economy ◽  
African Elephant ◽  
Metabolic Energy ◽  
Energetic Cost ◽  
Allometric Relationships ◽  
Cost Of Locomotion ◽  
Biological Laws ◽  
Large Animals ◽  
The Cost

Large animals have a much better fuel economy than small ones, both when they rest and when they run. At rest, each gram of tissue of the largest land animal, the African elephant, consumes metabolic energy at 1/20 the rate of a mouse; using existing allometric relationships, we calculate that it should be able to carry 1 g of its tissue (or a load) for 1 km at 1/40 the cost for a mouse. These relationships between energetics and size are so consistent that they have been characterized as biological laws. The elephant has massive legs and lumbers along awkwardly, suggesting that it might expend more energy to move about than other animals. We find, however, that its energetic cost of locomotion is predicted remarkably well by the allometric relationships and is the lowest recorded for any living land animal.

scholarly journals Post-synaptic morphology of mouse neuromuscular junctions is linked to muscle fibre type

2020 ◽  
Author(s):  
Aleksandra M. Mech ◽  
Anna-Leigh Brown ◽  
Giampietro Schiavo ◽  
James N. Sleigh
Keyword(s):  
Motor Neuron ◽  
Muscle Fibre ◽  
Fibre Type ◽  
Neuromuscular Junctions ◽  
Fibre Diameter ◽  
Neuromuscular Diseases ◽  
Neuronal Morphology ◽  
Muscle Fibre Type ◽  
Muscle Membrane ◽  
Muscle Fibres

AbstractThe neuromuscular junction (NMJ) is the highly specialised peripheral synapse formed between lower motor neuron terminals and muscle fibres. Post-synaptic acetylcholine receptors (AChRs), which are found in high density in the muscle membrane, bind to acetylcholine released into the synaptic cleft of the NMJ, ultimately facilitating the conversion of motor action potentials to muscle contractions. NMJs have been studied for many years as a general model for synapse formation, development and function, and are known to be early sites of pathological changes in many neuromuscular diseases. However, information is limited on the diversity of NMJs in different muscles, whether muscle fibre type impacts NMJ morphology and growth, and the relevance of these parameters to neuropathology. Here, this crucial gap was addressed using a robust and standardised semi-automated workflow called NMJ-morph to quantify features of pre- and post-synaptic NMJ architecture in an unbiased manner. Five wholemount muscles from wild-type mice were dissected and compared at immature (post-natal day, P7) and early adult (P31-32) timepoints. Post-synaptic AChR morphology was found to be more variable between muscles than that of the motor neuron terminal and there were greater differences in the developing NMJ than at the mature synapse. Post-synaptic architecture, but not neuronal morphology or post-natal synapse growth, correlates with fibre type and is largely independent of muscle fibre diameter. Counter to previous observations, this study indicates that smaller NMJs tend to innervate muscles with higher proportions of fast twitch fibres and that NMJ growth rate is not conserved across all muscles. Furthermore, healthy pre- and post-synaptic NMJ morphological parameters were collected for five anatomically and functionally distinct mouse muscles, generating reference data that will be useful for the future assessment of neuromuscular disease models.Graphical Abstract

Efficiency of uphill locomotion in nocturnal and diurnal lizards

1996 ◽  
Vol 199 (3) ◽  
pp. 587-592 ◽  
Author(s):  
C Farley ◽  
M Emshwiller
Keyword(s):  
Body Mass ◽  
Low Cost ◽  
Minimum Cost ◽  
Mechanical Work ◽  
Energetic Cost ◽  
Cost Of Transport ◽  
Unit Distance ◽  
Cost Of Locomotion ◽  
Average Body Mass ◽  
Average Body

Nocturnal geckos can walk on level ground more economically than diurnal lizards. One hypothesis for why nocturnal geckos have a low cost of locomotion is that they can perform mechanical work during locomotion more efficiently than other lizards. To test this hypothesis, we compared the efficiency of the nocturnal gecko Coleonyx variegatus (average body mass 4.2 g) and the diurnal skink Eumeces skiltonianus (average body mass 4.8 g) when they performed vertical work during uphill locomotion. We measured the rate of oxygen consumption when each species walked on the level and up a 50 slope over a range of speeds. For Coleonyx variegatus, the energetic cost of traveling a unit distance (the minimum cost of transport, Cmin) increased from 1.5 to 2.7 ml O2 kg-1 m-1 between level and uphill locomotion. For Eumeces skiltonianus, Cmin increased from 2.5 to 4.7 ml O2 kg-1 m-1 between level and uphill locomotion. By taking the difference between Cmin for level and uphill locomotion, we found that the efficiency of performing vertical work during locomotion was 37 % for Coleonyx variegatus and 19 % for Eumeces skiltonianus. The similarity between the 1.9-fold difference in vertical efficiency and the 1.7-fold difference in the cost of transport on level ground is consistent with the hypothesis that nocturnal geckos have a lower cost of locomotion than other lizards because they can perform mechanical work during locomotion more efficiently.

Rat diaphragm during postnatal development. I. Changes in distribution of muscle fibre type and in oxidative potential

1996 ◽  
Vol 8 (3) ◽  
pp. 391 ◽  
Author(s):  
MD Fratacci ◽  
M Levame ◽  
A Rauss ◽  
H Bousbaa ◽  
G Atlan
Keyword(s):  
Muscle Fibre ◽  
Fibre Type ◽  
Oxidative Capacity ◽  
Cross Sectional Area ◽  
Fibre Types ◽  
Type I ◽  
Sectional Area ◽  
Rat Diaphragm ◽  
Oxidative Potential ◽  
Cross Sectional

The changes occurring in the histochemical characteristics of the rat diaphragm during the postnatal period were examined. Fibre-type distribution, fibre oxidative capacity, i.e. succinate-dehydrogenase (SDH) activity, and cross-sectional area were compared in the costal (COS) and crural (CRU) regions, and across their abdominal and thoracic surfaces. The proportions of type I and IIb fibres in both COS and CRU increased with age, while the proportion of type IIa fibres progressively decreased. For COS, fibre distribution was homogeneous over the entire muscle and did not change after 4 weeks. For CRU, it was heterogeneous with a higher proportion of type I fibres on the thoracic surface as from the first week. All fibre types significantly increased in cross-sectional area between 1 and 8 weeks, with no significant differences in COS and CRU. Mean SDH activity did not differ between COS and CRU or across the muscles. Mean SDH activities-were low and identical in all fibre types at birth, and then increased, peaking at the 6th week in type I and IIa fibres. When total muscle fibre oxidative capacity was calculated from an index including fibre-type proportion, cross-sectional area and mean SDH activity, it was significantly higher at 1 than at 8 weeks after birth; this might have functional implications for the newborn.

Form and classification of motor endings in mammalian muscle spindles

1985 ◽  
Vol 225 (1239) ◽  
pp. 195-212 ◽  
Keyword(s):  
Muscle Fibre ◽  
Fibre Type ◽  
Muscle Spindles ◽  
Muscle Fibre Type ◽  
Motor Axon ◽  
Muscle Fibres ◽  
Intrafusal Muscle ◽  
Axon Terminals ◽  
Hindlimb Muscle

The presynaptic features of 234 motor endings supplied to cat hindlimb muscle spindles have been studied in teased, silver preparations, and the postsynaptic features of a further 27 endings have been studied in serial, 1 μm thick, transverse sections. In the presynaptic study motor endings received by the three types of intrafusal muscle fibre were compared with the endings supplied to spindles by the various functional categories of motor axon. Three forms of motor ending were found that had significantly different presynaptic features. These forms correspond closely to those previously identified in the literature as p 1 (β), p 2 (dynamic γ) and trail (static γ). The results of the postsynaptic study showed that the degree of indentation of the intrafusal muscle fibres by motor axon terminals increases with greater distance from the primary ending, irrespective of muscle-fibre type. We conclude that the postsynaptic form of intrafusal motor endings is determined by distance from primary ending and muscle-fibre type. It is not determined by type of motor axon, and cannot be correlated with presynaptic form so as to produce a unified classification of intrafusal motor endings.

Energetic cost of locomotion in the tammar wallaby

1992 ◽  
Vol 262 (5) ◽  
pp. R771-R778 ◽  
Author(s):  
R. V. Baudinette ◽  
G. K. Snyder ◽  
P. B. Frappell
Keyword(s):  
Oxygen Consumption ◽  
Blood Lactate ◽  
Body Mass ◽  
Energy Cost ◽  
Physiological Adaptation ◽  
Energetic Cost ◽  
Cost Of Locomotion ◽  
Lactate Levels ◽  
Energy Cost Of Locomotion ◽  
Blood Lactate Levels

Rates of oxygen consumption and blood lactate levels were measured in tammar wallabies (Macropus eugenii) trained to hop on a treadmill. In addition, the work required to overcome wind resistance during forward locomotion was measured in a wind tunnel. Up to approximately 2.0 m/s, rates of oxygen consumption increased linearly with speed and were not significantly different from rates of oxygen consumption for a quadruped of similar body mass. Between 2.0 and 9.4 m/s, rates of oxygen consumption were independent of hopping speed, and between 3.9 and 7.9 m/s, the range over which samples were obtained, blood lactate levels were low (0.83 +/- 0.13 mmol.min-1.kg-1) and did not increase with hopping speed. The work necessary to overcome drag increased exponentially with speed but increased the energy cost of locomotion by only 10% at the average speed attained by our fast hoppers. Thus, during hopping, the energy cost of locomotion is effectively independent of speed. At rates of travel observed in the field, the estimated energy cost of transport in large macropods is less than one-third the cost for a quadruped of equivalent body mass. The energetic savings associated with this unique form of locomotion may have been an important physiological adaptation, enabling large macropods to efficiently cover the distances necessary to forage in the semiarid landscapes of Australia.

scholarly journals Effect of Age and Sex on Histomorphometrical Characteristics of Two Muscles of Laticauda Lambs

2010 ◽  
Vol 79 (1) ◽  
pp. 3-12 ◽  
Author(s):  
Salvatore Velotto ◽  
Ettore Varricchio ◽  
Maria Rosa Di Prisco ◽  
Tommaso Stasi ◽  
Antonio Crasto
Keyword(s):  
Muscle Fibre ◽  
Fibre Type ◽  
Succinic Dehydrogenase ◽  
Longissimus Dorsi ◽  
Multiple Birth ◽  
Muscle Fibres ◽  
Type Area ◽  
Muscle Tissues ◽  
Slow Twitch ◽  
Fast Twitch

The aim of the present experiment was to determine the effect of sex and age on histochemical and morphometric characteristics of muscle fibres (myocytes) in lambs born by single, twin, triplet and quadruplet birth. Thirty lambs were slaughtered at 60 days of age; thirty were weaned at 60 days and fed until 120 days with flakes (60%) and food supplements, and then slaughtered. Muscle tissues were obtained from two muscles, namely m. semitendinosus and m. longissimus dorsi of all lambs. For each fibre type, area perimeter and diameter (maximum and minimum) were measured and slow-twitch oxidative fibres, fast-twitch glycolytic fibres, fast-twitch oxidative-glycolytic fibres were histochemically differentiated. The muscles were stained for myosin ATPase, and succinic dehydrogenase. At 60 days, females had fibres larger than males, whereas the opposite was observed at 120 days. Besides, at 60 days, the lambs born by single birth had fibres larger than those born by multiple birth, whereas the opposite was observed at 120 days. Single lambs were heavier than twin lambs and multiple lambs. Fast-twitch glycolytic fibres had the largest size, followed by slow-twitch oxidative and fast-twitch oxidative glycolytic fibres. The dimensions of fibre types in m. longissimus dorsi were larger than in m. semitendinosus (P < 0.001).These muscle fibre characteristics are thought to be important factors influencing meat quality, which is often related to metabolic and contractile properties as determined by the muscle fibre type distribution.

The effect of maternal undernutrition on muscle fibre type in the newborn lamb

2003 ◽  
Vol 2003 ◽  
pp. 60-60
Author(s):  
A.J. Fahey ◽  
J.M. Brameld ◽  
T. Parr ◽  
P.J. Buttery
Keyword(s):  
Muscle Fibre ◽  
Meat Quality ◽  
Fibre Type ◽  
Muscle Development ◽  
Nutrient Supply ◽  
Muscle Fibre Type ◽  
Growth Potential ◽  
Muscle Fibres ◽  
General Hypothesis ◽  
Maternal Undernutrition

Muscle fibre type can influence meat quality (Maltinet al1997). Muscle fibre formation occurs during gestation and in the sheep the total number of fibres in a muscle is essentially fixed at birth. (Ashmereet al1972). Postnatal growth of muscle is entirely due to elongation and widening of the existing muscle fibres. Therefore the gestational period is important in the long-term growth potential of the animal. By investigating changes in muscle fibre type, the aim of this study was to test the general hypothesis that the poor carcass quality sometimes seen in ruminant animals may be due to poor nutrition at strategic time points during the animal’s development. As agricultural practices continue to become more extensive, variation in the nutrient supply to the animal is becoming more common. Therefore it is important to understand the effect of any changes in nutrient supply to the mother, during gestation on the subsequent muscle development of the fetus and ultimately the effects on meat quality.

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