scholarly journals Noncontractile tissue forces mask muscle fiber forces underlying muscle spindle Ia afferent firing rates in stretch of relaxed rat muscle

2018 ◽  
Author(s):  
Kyle P. Blum ◽  
Paul Nardelli ◽  
Timothy C. Cope ◽  
Lena H. Ting
Keyword(s):  
Muscle Fiber ◽  
Muscle Spindle ◽  
Muscle Force ◽  
Muscle Fibers ◽  
Elastic Tissue ◽  
Tissue Model ◽  
Firing Rates ◽  
Ia Afferent ◽  
Rat Muscle ◽  
Cross Bridges

AbstractStretches of relaxed cat and rat muscle elicit similar history-dependent muscle spindle Ia firing rates that resemble history-dependent forces seen in single activated muscle fibers (Nichols and Cope, 2004). During stretch of relaxed cat muscle, whole musculotendon forces exhibit history-dependence that mirror history-dependent muscle spindle firing rates, where both muscle force and muscle spindle firing rates are elevated in the first stretch in a series of stretch-shorten cycles (Blum et al., 2017). By contrast, rat musculotendon are only mildly history-dependent and do not mirror history-dependent muscle spindle firing rates in the same way (Haftel et al., 2004). We hypothesized that history-dependent muscle spindle firing rates elicited in stretch of relaxed rat muscle would mirror history-dependent muscle fiber forces, which are masked by noncontractile tissue at the level of whole musculotendon force. We removed noncontractile tissue force contributions from the recorded musculotendon force using an exponentially-elastic tissue model. We then show that the remaining estimated muscle fiber force resembles history-dependent muscle spindle firing rates recorded simultaneously. These forces also resemble history-dependent forces recorded in stretch of single activated fibers and attributed to muscle cross-bridge mechanisms (Campbell and Moss, 2000). Our results suggest that history-dependent muscle spindle firing in both rats and cats arise from stretch of cross-bridges in muscle fibers.

scholarly journals Elastic tissue forces mask muscle fiber forces underlying muscle spindle Ia afferent firing rates in stretch of relaxed rat muscle

2019 ◽  
Vol 222 (15) ◽  
pp. jeb196287 ◽  
Author(s):  
Kyle P. Blum ◽  
Paul Nardelli ◽  
Timothy C. Cope ◽  
Lena H. Ting
Keyword(s):  
Muscle Fiber ◽  
Muscle Spindle ◽  
Elastic Tissue ◽  
Firing Rates ◽  
Ia Afferent ◽  
Rat Muscle

Anisotropic diffusion of oxygen in slices of rat muscle

1984 ◽  
Vol 246 (1) ◽  
pp. R107-R113 ◽  
Author(s):  
L. D. Homer ◽  
J. B. Shelton ◽  
C. H. Dorsey ◽  
T. J. Williams
Keyword(s):  
Diffusion Coefficient ◽  
Fluorescence Quenching ◽  
Muscle Fiber ◽  
Extracellular Space ◽  
Anisotropic Diffusion ◽  
Muscle Fibers ◽  
Rat Muscle ◽  
Hamstring Muscles ◽  
Standard Deviations ◽  
Diffusion Coefficient Of Oxygen

The diffusion coefficient of oxygen (D) and the fluorescence quenching coefficient (K') of pyrenebutyric acid (PBA) were measured in sections of rat hamstring muscles. Values of D and K' at temperatures (Tc) of 20, 30, and 40 degrees C were determined and referred to the values in water. In sections cut parallel to the muscle fibers, D = DH2O (0.380 +/- 0.038), whereas in sections cut across the grain of the fibers, D = DH2O (0.985 +/- 0.039). Oxygen diffuses along the length of a muscle fiber over twice as rapidly as it diffuses in directions perpendicular to the long axis of the fiber. This suggests that fibers, myofibrils, or myofilaments offer substantial barriers to the diffusion of oxygen, whereas extracellular space and spaces around fibers or myofibrils or myofilaments offer no more resistance than water to the diffusion of oxygen. Corresponding estimates for K' were K' = K'H2O[0.14 (1 + 0.25 Tc)] and K' = K'H2O[0.21 (1 + 0.25 Tc)] for slices cut parallel to the long axis of muscle fibers and across the long axis, respectively. Standard deviations of K' were 9%.

scholarly journals Loss of muscle strength during sepsis is in part regulated by glucocorticoids and is associated with reduced muscle fiber stiffness

2012 ◽  
Vol 303 (10) ◽  
pp. R1090-R1099 ◽  
Author(s):  
Nima Alamdari ◽  
Gianluca Toraldo ◽  
Zaira Aversa ◽  
Ira Smith ◽  
Estibaliz Castillero ◽  
...  
Keyword(s):  
Muscle Strength ◽  
Muscle Weakness ◽  
Muscle Fiber ◽  
Muscle Fibers ◽  
Cecal Ligation ◽  
Treatment Strategies ◽  
Skinned Muscle ◽  
Cross Bridges ◽  
New Treatment

Sepsis is associated with impaired muscle function but the role of glucocorticoids in sepsis-induced muscle weakness is not known. We tested the role of glucocorticoids in sepsis-induced muscle weakness by treating septic rats with the glucocorticoid receptor antagonist RU38486. In addition, normal rats were treated with dexamethasone to further examine the role of glucocorticoids in the regulation of muscle strength. Sepsis was induced in rats by cecal ligation and puncture, and muscle force generation (peak twitch and tetanic tension) was determined in lower extremity muscles. In other experiments, absolute and specific force as well as stiffness (reflecting the function of actomyosin cross bridges) were determined in isolated skinned muscle fibers from control and septic rats. Sepsis and treatment with dexamethasone resulted in reduced maximal twitch and tetanic force in intact isolated extensor digitorum longus muscles. The absolute and specific maximal force in isolated muscle fibers was reduced during sepsis together with decreased fiber stiffness. These effects of sepsis were blunted (but not abolished) by RU38486. The results suggest that muscle weakness during sepsis is at least in part regulated by glucocorticoids and reflects loss of contractility at the cellular (individual muscle fiber) level. In addition, the results suggest that reduced function of the cross bridges between actin and myosin (documented as reduced muscle fiber stiffness) may be involved in sepsis-induced muscle weakness. An increased understanding of mechanisms involved in loss of muscle strength will be important for the development of new treatment strategies in patients with this debilitating consequence of sepsis.

scholarly journals Development of a human neuromuscular tissue-on-a-chip model on a 24-well-plate-format compartmentalized microfluidic device

Lab on a Chip ◽  
2021 ◽  
Author(s):  
Kazuki Yamamoto ◽  
Nao Yamaoka ◽  
Yu Imaizumi ◽  
Takunori Nagashima ◽  
Taiki Furutani ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Microfluidic Device ◽  
Motor Neurons ◽  
Muscle Fibers ◽  
Three Dimensional ◽  
Tissue Model ◽  
Skeletal Muscle Fibers

A three-dimensional human neuromuscular tissue model that mimics the physically separated structures of motor neurons and skeletal muscle fibers is presented.

scholarly journals Frozen/thawed meat quality associated with muscle fiber characteristics of porcine longissimus thoracis et lumborum, psoas major, semimembranosus, and semitendinosus muscles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Huilin Cheng ◽  
Sumin Song ◽  
Gap-Don Kim
Keyword(s):  
Meat Quality ◽  
Muscle Fiber ◽  
Shear Force ◽  
Muscle Fibers ◽  
Frozen Storage ◽  
Meat Color ◽  
Pork Meat ◽  
Psoas Major ◽  
The Relationship

AbstractTo evaluate the relationship between muscle fiber characteristics and the quality of frozen/thawed pork meat, four different muscles, M. longissimus thoracis et lumborum (LTL), M. psoas major (PM), M. semimembranosus (SM), and M. semitendinosus (ST), were analyzed from twenty carcasses. Meat color values (lightness, redness, yellowness, chroma, and hue) changed due to freezing/thawing in LTL, which showed larger IIAX, IIX, and IIXB fibers than found in SM (P < 0.05). SM and ST showed a significant decrease in purge loss and an increase in shear force caused by freezing/thawing (P < 0.05). Compared with LTL, SM contains more type IIXB muscle fibers and ST had larger muscle fibers I and IIA (P < 0.05). PM was the most stable of all muscles, since only its yellowness and chroma were affected by freezing/thawing (P < 0.05). These results suggest that pork muscle fiber characteristics of individual cuts must be considered to avoid quality deterioration during frozen storage.

Effects of ?-endorphin on the development of denervation changes in rat muscle fiber membrane

1988 ◽  
Vol 19 (6) ◽  
pp. 550-555 ◽  
Author(s):  
A. V. Chikin ◽  
A. Kh. Urazaev ◽  
E. M. Volkov ◽  
G. I. Poletaev ◽  
Kh. S. Khamitov
Keyword(s):  
Muscle Fiber ◽  
Fiber Membrane ◽  
Rat Muscle ◽  
Muscle Fiber Membrane

scholarly journals FINE STRUCTURE OF RAT INTRAFUSAL MUSCLE FIBERS

1971 ◽  
Vol 51 (1) ◽  
pp. 83-103 ◽  
Author(s):  
William K. Ovalle
Keyword(s):  
Muscle Fiber ◽  
Muscle Fibers ◽  
Muscle Spindles ◽  
Intrafusal Muscle ◽  
Dense Granules ◽  
Intrafusal Muscle Fibers ◽  
Sarcotubular System ◽  
Nuclear Chain ◽  
T System ◽  
Nuclear Bag

An ultrastructural comparison of the two types of intrafusal muscle fibers in muscle spindles of the rat was undertaken. Discrete myofibrils with abundant interfibrillar sarcoplasm and organelles characterize the nuclear chain muscle fiber, while a continuous myofibril-like bundle with sparse interfibrillar sarcoplasm distinguishes the nuclear bag muscle fiber. Nuclear chain fibers possess well-defined and typical M bands in the center of each sarcomere, while nuclear bag fibers contain ill-defined M bands composed of two parallel thin densities in the center of the pseudo-H zone of each sarcomere. Mitochondria of nuclear chain fibers are larger and more numerous than they are in nuclear bag fibers. Mitochondria of chain fibers, in addition, often contain conspicuous dense granules, and they are frequently intimately related to elements of the sarcoplasmic reticulum (SR). Striking differences are noted in the organization and degree of development of the sarcotubular system. Nuclear bag fibers contain a poorly developed SR and T system with only occasional junctional couplings (dyads and triads). Nuclear chain fibers, in contrast, possess an unusually well-developed SR and T system and a variety of multiple junctional couplings (dyads, triads, quatrads, pentads, septads). Greatly dilated SR cisternae are common features of nuclear chain fibers, often forming intimate associations with T tubules, mitochondria, and the sarcolemma. Such dilatations of the SR were not encountered in nuclear bag fibers. The functional significance of these structural findings is discussed.

A semi-automated measurement of muscle fiber size using the Imaris software

2021 ◽  
Author(s):  
Jennifer E. Gilda ◽  
Joon-Hyuk Ko ◽  
Aviv-Yvonne Elfassy ◽  
Nadav Tropp ◽  
Anna Parnis ◽  
...  
Keyword(s):  
Muscle Atrophy ◽  
Muscle Fiber ◽  
Cross Sections ◽  
Statistical Tests ◽  
Muscle Fibers ◽  
Fluorescent Labeling ◽  
Cross Sectional ◽  
Short Period ◽  
Fiber Size ◽  
Specific Protease

The size and shape of skeletal muscle fibers are affected by various physiological and pathological conditions, such as muscle atrophy, hypertrophy, regeneration, and dystrophies. Hence, muscle fiber cross-sectional area (CSA) is an important determinant of muscle health and plasticity. We adapted the Imaris software to automatically segment muscle fibers based on fluorescent labeling of the plasma membrane, and measure muscle fiber CSA. Analysis of muscle cross sections by the Imaris semi-automated and manual approaches demonstrated a similar decrease in CSA of atrophying muscles from fasted mice compared with fed controls. In addition, we previously demonstrated that downregulation of the Ca2+-specific protease calpain-1 attenuates muscle atrophy. Accordingly, both the Imaris semi-automated and manual approaches showed a similar increase in CSA of fibers expressing calpain-1 shRNA compared with adjacent non-transfected fibers in the same muscle cross section. Although both approaches seem valid for measurements of muscle fiber size, the manual marking method is less preferable because it is highly time-consuming, subjective, and limits the number of cells that can be analyzed. The Imaris semi-automated approach is user-friendly, requires little training or optimization, and can be used to efficiently and accurately mark thousands of fibers in a short period of time. As a novel addition to the commonly used statistics, we also describe statistical tests that quantify the strength of an effect on fiber size, enabling detection of significant differences between skewed distributions that would otherwise not be detected using typical methods.

Motoneuron and muscle fiber succinate dehydrogenase activity in control and overloaded plantaris

1991 ◽  
Vol 71 (4) ◽  
pp. 1589-1592 ◽  
Author(s):  
G. R. Chalmers ◽  
R. R. Roy ◽  
V. R. Edgerton
Keyword(s):  
Succinate Dehydrogenase ◽  
Muscle Fiber ◽  
Muscle Fibers ◽  
Cell Types ◽  
Mitochondrial Proteins ◽  
Succinate Dehydrogenase Activity ◽  
Fiber Size ◽  
The Right ◽  
Gastrocnemius Muscles ◽  
Selective Increase

To determine the level of coordination in succinate dehydrogenase (SDH) activity between plantaris motoneurons and muscle fibers, the soleus and gastrocnemius muscles were bilaterally excised in four cats to subject the plantaris to functional overload (FO). Five normal cats served as controls. Twelve weeks after surgery the right plantaris in each cat was injected with horseradish peroxidase to identify plantaris motoneurons. SDH activity then was measured in a population of plantaris motoneurons and muscle fibers in each cat. Control motoneurons and muscle fibers had similar mean SDH activities and a similar relationship between cell size and SDH activity. After FO, muscle fiber size doubled and mean muscle fiber SDH activity halved. Motoneuron mean SDH activity and size were unaffected by FO. Total SDH activity was unchanged in both the motoneurons and muscle fibers after FO. These changes suggest a selective increase in contractile proteins with little or no modulation of mitochondrial proteins in the muscle fibers, because total SDH activity was unchanged in muscle fibers after FO. These data demonstrate that although mean SDH activities were similar in control motoneurons and muscle fibers, mean SDH activities in these two cell types can change independently.

Exercise-induced focal skeletal muscle fiber degeneration and capillary morphology

1989 ◽  
Vol 66 (6) ◽  
pp. 2857-2865 ◽  
Author(s):  
F. M. Peeze Binkhorst ◽  
H. Kuipers ◽  
J. Heymans ◽  
P. M. Frederik ◽  
D. W. Slaaf ◽  
...  
Keyword(s):  
Blood Flow ◽  
Muscle Fiber ◽  
Cross Sections ◽  
Muscle Fibers ◽  
Basal Membrane ◽  
Cross Sectional ◽  
Male Wistar Rats ◽  
Muscle Water Content ◽  
Exercise Muscle ◽  
Exercise Induced

The relationship between exercise-induced focal muscle fiber degeneration and changes in capillary morphology was investigated in male Wistar rats. Untrained animals ran on a treadmill for 1 h at submaximal intensity and were killed 0, 6, or 24 h after running. Nonexercised rats served as controls. In situ perfused soleus muscles were prepared for electron microscopy. Micrographed cross sections were quantitatively analyzed for parameters indicative of capillary blood flow or transcapillary exchange. Capillary lumina were ovally rather than circularly shaped, and no indications for obstruction of blood flow at the capillary level were found. Endothelial cells and their organelles had a normal appearance in all groups. However, immediately after exercise, capillaries showed a decreased thickness of their endothelium and basal membrane, probably caused by dehydration. Six hours after exercise, muscle fibers were swollen (28% increase in cross-sectional area), resulting in a slightly increased diffusion distance. This fiber swelling was not associated with an increase in muscle water content, a finding for which no explanation could be found. Twenty-four hours after the animals ran, capillaries located near degenerated muscle fibers had an increased cross-sectional luminal area and an increased luminal circumference. This effect decreased gradually with increasing distance from the degenerated fiber area. The present morphometric results do not support the hypothesis that changes in capillary morphology primarily contribute to exercise-induced focal muscle fiber degeneration.

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