scholarly journals In Vivo Measurement of Hindlimb Dorsiflexor Isometric Torque from Pig

10.3791/62905 ◽  
2021 ◽  
Author(s):  
Benjamin T. Corona ◽  
Jarrod A. Call ◽  
Matthew Borkowski ◽  
Sarah M. Greising
Keyword(s):  
Isometric Torque

A stimulating nerve cuff for chronic in vivo measurements of torque produced about the ankle in the mouse

1998 ◽  
Vol 84 (6) ◽  
pp. 2171-2176 ◽  
Author(s):  
Gordon L. Warren ◽  
Christopher P. Ingalls ◽  
R. B. Armstrong
Keyword(s):  
Motor Nerve ◽  
Tibialis Anterior Muscle ◽  
Common Peroneal Nerve ◽  
Success Rates ◽  
Nerve Cuff ◽  
Isometric Torque ◽  
Electromyographic Signal ◽  
Specific Muscle ◽  
Implantation Success

Specific muscle training and chronic contractile measurements are difficult in rodents, especially in the mouse. The primary reason for this is the lack of a means for stimulating the motor nerve that does not damage the nerve and that permits reproducible measurements of contractility. In this paper, we describe procedures for the construction and implantation of a stimulating nerve cuff for use on the mouse common peroneal nerve. We demonstrate that nerve cuff implantation success rates can be high (i.e., 75–93%), as determined from measurements of maximal isometric torque produced by the anterior crural muscles. Isometric torque production is not adversely affected by the nerve cuff because the torque produced matches that observed in our established percutaneous stimulation model. We also demonstrate that use of the nerve cuff for stimulation is compatible with electromyographic measurements made on the tibialis anterior muscle, with no sign of stimulation artifact in the electromyographic signal.

Importance of satellite cells in the strength recovery after eccentric contraction-induced muscle injury

2003 ◽  
Vol 285 (6) ◽  
pp. R1490-R1495 ◽  
Author(s):  
Christopher R. Rathbone ◽  
J. C. Wenke ◽  
Gordon L. Warren ◽  
R. B. Armstrong
Keyword(s):  
Cell Proliferation ◽  
Satellite Cell ◽  
Muscle Injury ◽  
Common Peroneal Nerve ◽  
Eccentric Contraction ◽  
Γ Irradiation ◽  
Force Recovery ◽  
Isometric Torque ◽  
Satellite Cell Proliferation

The purpose of this study was to determine if the elimination of satellite cell proliferation using γ-irradiation would inhibit normal force recovery after eccentric contraction-induced muscle injury. Adult female ICR mice were implanted with a stimulating nerve cuff on the common peroneal nerve and assigned to one of four groups: 1) irradiation- and eccentric contraction-induced injury, 2) eccentric contraction-induced injury only, 3) irradiation only, and 4) no intervention. Anterior crural muscles were irradiated with a dose of 2,500 rad and injured with 150 in vivo maximal eccentric contractions. Maximal isometric torque was determined weekly through 35 days postinjury. Immediately after injury, maximal isometric torque was reduced by ∼50% and had returned to normal by 28 days postinjury in the nonirradiated injured mice. However, torque production of irradiated injured animals did not recover fully and was 25% less than that of injured nonirradiated mice 35 days postinjury. These data suggest that satellite cell proliferation is required for approximately half of the force recovery after eccentric contraction-induced injury.

The Influence of Fascicle Behavior on the Lack of Velocity Dependence in Eccentric Joint Torque in Humans: In Vivo Observation

2009 ◽  
Vol 25 (2) ◽  
pp. 111-118 ◽  
Author(s):  
Kentaro Chino ◽  
Naotoshi Mitsukawa ◽  
Kai Kobayashi ◽  
Yusuke Miyoshi ◽  
Toshiaki Oda ◽  
...  
Keyword(s):  
Plantar Flexion ◽  
Triceps Surae ◽  
Joint Torque ◽  
Fascicle Length ◽  
Significant Difference ◽  
Isometric Torque ◽  
The Difference ◽  
The Relationship ◽  
Real Time Ultrasonography

To investigate the relationship between fascicle behavior and joint torque, the fascicle behavior of the triceps surae during isometric and eccentric (30 and 60 deg/s) plantar flexion by maximal voluntary and submaximal electrical activation (MVA and SEA) was measured by real-time ultrasonography. Eccentric torque at 30 and 60 deg/s was significantly higher than isometric torque under SEA, but not under MVA. However, fascicle length did not significantly differ between isometric and eccentric trials under either condition. Therefore, the difference in developed torque by MVA and SEA cannot be explained by fascicle behavior. Under both MVA and SEA conditions, eccentric torque at 30 and 60 deg/s was equivalent. Similarly, fascicle lengthening velocities at 30 and 60deg/s did not show any significant difference. Such fascicle behavior can be attributed to the influence of tendinous tissue and pennation angle, and lead to a lack of increase in eccentric torque with increasing angular velocity.

Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice.

2021 ◽  
Author(s):  
Seongkyun Lim ◽  
J. William Deaver ◽  
Megan E. Rosa-Caldwell ◽  
Wesley S. Haynie ◽  
Francielly Morena Da Silva ◽  
...  
Keyword(s):  
Time Course ◽  
Cancer Cachexia ◽  
Contractile Function ◽  
Tumor Bearing ◽  
Synthetic Rate ◽  
Fractional Synthetic Rate ◽  
Isometric Torque ◽  
Muscle Contractile

Cancer cachexia (CC) results in impaired muscle function and quality of life and is the primary cause of death for ~20-30% of cancer patients. We demonstrated mitochondrial degeneration as a precursor to CC in male mice, however, if such alterations occur in females is currently unknown. The purpose of this study was to elucidate muscle alterations in CC development in female tumor-bearing mice. 60 female C57BL/6J mice were injected with PBS or Lewis Lung Carcinoma at 8-week age, and tumors developed for 1, 2, 3, or 4 weeks to assess the time course of cachectic development. In vivo muscle contractile function, protein fractional synthetic rate (FSR), protein turnover, and mitochondrial health were assessed. 3- and 4-week tumor-bearing mice displayed a dichotomy in tumor growth and were reassigned to High Tumor (HT) and Low Tumor (LT) groups. HT mice exhibited lower soleus, TA, and fat weights compared to PBS. HT mice showed lower peak isometric torque and slower one-half relaxation time compared to PBS. HT mice had lower FSR compared to PBS while E3 ubiquitin ligases were greater in HT compared to other groups. Bnip3 (mitophagy) and pMitoTimer red puncta (mitochondrial degeneration) were greater in HT while Pgc1α1 and Tfam (mitochondrial biogenesis) were lower in HT compared to PBS. We demonstrate alterations in female tumor-bearing mice where HT exhibited greater protein degradation, impaired muscle contractility, and mitochondrial degeneration compared to other groups. Our data provide novel evidence for a distinct cachectic development in tumor-bearing female mice compared to previous male studies.

Preconditioning contractions prevent prolonged force depression and Ca2+-dependent proteolysis of STAC3 after damaging eccentric contractions

2021 ◽  
Author(s):  
Yuki Ashida ◽  
Koichi Himori ◽  
Katsuyuki Tamai ◽  
Iori Kimura ◽  
Takashi Yamada
Keyword(s):  
Medial Gastrocnemius ◽  
Eccentric Contractions ◽  
Blue Dye ◽  
Calpain Inhibitor ◽  
Rich Domain ◽  
Force Depression ◽  
Isometric Torque ◽  
Domain 3 ◽  
Subsequent Activation

Preconditioning contractions (PCs) have been shown to markedly improve recovery from eccentric contractions (ECCs)-induced force depression. We here examined the mechanism behind the effects of PCs with focusing on the SH3 and cysteine rich domain 3 (STAC3) that is essential for coupling membrane depolarization to Ca2+ release from the sarcoplasmic reticulum. Rat medial gastrocnemius (MG) muscles were excised immediately (REC0), 1 day (REC1), and 4 days (REC4) after exposure to 100 repeated damaging ECCs in vivo. PCs with 10 repeated non-damaging ECCs were applied 2 days before the damaging ECCs. Damaging ECCs induced in vivo isometric torque depression at 50 and 100 Hz stimulation frequencies, which was accompanied by a significant decrease in the amount of full-length STAC3, an activation of calpain 1, and an increased number of Evans Blue dye positive fibers in MG muscles at REC1 and REC4. Interestingly, PCs attenuated all these deleterious alterations induced by damaging ECCs. Moreover, mechanistic experiments performed on normal muscle samples exposed to various concentration of Ca2+ showed a Ca2+-dependent proteolysis of STAC3, which was prevented by calpain inhibitor MDL-28170. In conclusion, PCs may improve recovery from force depression after damaging ECCs, in part by inhibiting the loss of STAC3 due to the increased permeability of cell membrane and subsequent activation of calpain 1.

scholarly journals Adaptive strength gains in dystrophic muscle exposed to repeated bouts of eccentric contraction

2011 ◽  
Vol 111 (6) ◽  
pp. 1768-1777 ◽  
Author(s):  
Jarrod A. Call ◽  
Michael D. Eckhoff ◽  
Kristen A. Baltgalvis ◽  
Gordon L. Warren ◽  
Dawn A. Lowe
Keyword(s):  
Functional Recovery ◽  
Extensor Digitorum Longus ◽  
Eccentric Contraction ◽  
Extensor Digitorum ◽  
Eccentric Contractions ◽  
Mdx Mice ◽  
Dystrophic Muscle ◽  
Generating Capacity ◽  
Isometric Torque

The objective of this study was to determine the functional recovery and adaptation of dystrophic muscle to multiple bouts of contraction-induced injury. Because lengthening (i.e., eccentric) contractions are extremely injurious for dystrophic muscle, it was considered that repeated bouts of such contractions would exacerbate the disease phenotype in mdx mice. Anterior crural muscles (tibialis anterior and extensor digitorum longus) and posterior crural muscles (gastrocnemius, soleus, and plantaris) from mdx mice performed one or five repeated bouts of 100 electrically stimulated eccentric contractions in vivo, and each bout was separated by 10–18 days. Functional recovery from one bout was achieved 7 days after injury, which was in contrast to a group of wild-type mice, which still showed a 25% decrement in electrically stimulated isometric torque at that time point. Across bouts there was no difference in the immediate loss of strength after repeated bouts of eccentric contractions for mdx mice (−70%, P = 0.68). However, after recovery from each bout, dystrophic muscle had greater torque-generating capacity such that isometric torque was increased ∼38% for both anterior and posterior crural muscles at bout 5 compared with bout 1 ( P < 0.001). Moreover, isolated extensor digitorum longus muscles excised from in vivo-tested hindlimbs 14–18 days after bout 5 had greater specific force than contralateral control muscles (12.2 vs. 10.4 N/cm2, P = 0.005) and a 20% greater maximal relaxation rate ( P = 0.049). Additional adaptations due to the multiple bouts of eccentric contractions included rapid recovery and/or sparing of contractile proteins, enhanced parvalbumin expression, and a decrease in fiber size variability. In conclusion, eccentric contractions are injurious to dystrophic skeletal muscle; however, the muscle recovers function rapidly and adapts to repeated bouts of eccentric contractions by improving strength.

Adaptation to lengthening contraction-induced injury in mouse muscle

2004 ◽  
Vol 97 (3) ◽  
pp. 1067-1076 ◽  
Author(s):  
Christopher P. Ingalls ◽  
J. C. Wenke ◽  
Talal Nofal ◽  
R. B. Armstrong
Keyword(s):  
Myofibrillar Protein ◽  
Rapid Loss ◽  
Lengthening Contractions ◽  
Mouse Muscle ◽  
Lengthening Contraction ◽  
Strength Recovery ◽  
Torque Loss ◽  
Rate Of Recovery ◽  
Isometric Torque

Adaptations to repeated bouts of injury-inducing lengthening contractions were studied in mouse anterior crural muscles. Five bouts of 150 lengthening contractions were performed in vivo, with each bout separated by 2 wk of rest. Three primary observations were made. First, there was little, if any, attenuation in the immediate isometric torque losses after lengthening contractions at “physiological” stimulation frequencies (i.e., <125 Hz), although there was a pronounced decrease in torque loss at higher frequencies between the first and second bouts. Second, the immediate losses in strength that occurred after all five lengthening contraction bouts could be explained in part by excitation-contraction uncoupling. Third, the most important adaptation was a significant enhancement in the rate of recovery of strength after the lengthening contractions. It is probable that the accelerated rate of strength recovery resulted from the more rapid loss and subsequent recovery of myofibrillar protein observed after the fifth bout.

Fine Structural Changes in the Microvasculature of the Mouse Pinna: Aging and Radiation Injury

1974 ◽  
Vol 32 ◽  
pp. 54-55
Author(s):  
S. Phyllis Steamer ◽  
Rosemarie L. Devine
Keyword(s):  
Structural Changes ◽  
Radiation Treatment ◽  
Arterial Stenosis ◽  
Ultrastructural Changes ◽  
Vascular Effects ◽  
Microvascular Changes ◽  
Surrounding Connective Tissue ◽  
Fission Neutrons ◽  
Total Body

The importance of radiation damage to the skin and its vasculature was recognized by the early radiologists. In more recent studies, vascular effects were shown to involve the endothelium as well as the surrounding connective tissue. Microvascular changes in the mouse pinna were studied in vivo and recorded photographically over a period of 12-18 months. Radiation treatment at 110 days of age was total body exposure to either 240 rad fission neutrons or 855 rad 60Co gamma rays. After in vivo observations in control and irradiated mice, animals were sacrificed for examination of changes in vascular fine structure. Vessels were selected from regions of specific interest that had been identified on photomicrographs. Prominent ultrastructural changes can be attributed to aging as well as to radiation treatment. Of principal concern were determinations of ultrastructural changes associated with venous dilatations, segmental arterial stenosis and tortuosities of both veins and arteries, effects that had been identified on the basis of light microscopic observations. Tortuosities and irregularly dilated vein segments were related to both aging and radiation changes but arterial stenosis was observed only in irradiated animals.

Induction and Differentiation of Dental Epithelium in Vivo and in Vitro

1982 ◽  
Vol 40 ◽  
pp. 142-145
Author(s):  
E. J. Kollar
Keyword(s):  
Connective Tissue ◽  
Oral Mucosa ◽  
Basal Lamina ◽  
Functional Derivatives ◽  
Specific Source ◽  
Dental Epithelium ◽  
Connective Tissue Stroma

The differentiation and maintenance of many specialized epithelial structures are dependent on the underlying connective tissue stroma and on an intact basal lamina. These requirements are especially stringent in the development and maintenance of the skin and oral mucosa. The keratinization patterns of thin or thick cornified layers as well as the appearance of specialized functional derivatives such as hair and teeth can be correlated with the specific source of stroma which supports these differentiated expressions.

Ultrastructural Correlations between Clonal Human Tumor Colonies and in Vivo Neoplasms

1982 ◽  
Vol 40 ◽  
pp. 210-211
Author(s):  
M.J. Murphy ◽  
R.R. Price ◽  
J.C. Sloman
Keyword(s):  
Cultured Cells ◽  
Human Tumor ◽  
Cell Type ◽  
Tumor Mass ◽  
Initial Cell ◽  
Cloning Assay ◽  
Human Tumor Cloning ◽  
The Relationship

The in vitro human tumor cloning assay originally described by Salmon and Hamburger has been applied recently to the investigation of differential anti-tumor drug sensitivities over a broad range of human neoplasms. A major problem in the acceptance of this technique has been the question of the relationship between the cultured cells and the original patient tumor, i.e., whether the colonies that develop derive from the neoplasm or from some other cell type within the initial cell population. A study of the ultrastructural morphology of the cultured cells vs. patient tumor has therefore been undertaken to resolve this question. Direct correlation was assured by division of a common tumor mass at surgical resection, one biopsy being fixed for TEM studies, the second being rapidly transported to the laboratory for culture.

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