The Journal of Physiology, ISSN 0022-3751, 12/2017, Volume 595, Issue 23, pp. 7123 - 7134
Key points Inactivation of a skeletal muscle results in slow to fast myosin heavy chain (MyHC) shift. AMP‐activated protein kinase (AMPK) can be implicated in...
AMPK | AICAR | MyHC | hindlimb unloading | soleus muscle | HDAC | HDAC4 | ADAPTIVE RESPONSES | PHYSIOLOGY | ACTIVATED PROTEIN-KINASE | STIMULATION | ATROPHY | PHOSPHORYLATION | TRANSCRIPTION | NEUROSCIENCES | TWITCH MUSCLE | SKELETAL-MUSCLE FIBERS | PLASTICITY | Protein Kinases - metabolism | Phosphorylation | Rats, Wistar | RNA, Messenger - genetics | Myosin Heavy Chains - genetics | Rats | Histone Deacetylases - metabolism | Male | Muscle Fibers, Skeletal - metabolism | RNA, Messenger - metabolism | Myosin Heavy Chains - metabolism | Animals | Cell Nucleus - metabolism | Hindlimb Suspension - adverse effects | Protein Processing, Post-Translational | Active Transport, Cell Nucleus | Muscles | Messenger RNA | T cells | Muscle proteins | Protein kinases | Myosin | Histone deacetylase | Transformation | Calcineurin | Genes | Gene regulation | Chains | Activation | Dephosphorylation | Soleus muscle | Kinases | AMP-activated protein kinase | Nuclei | Accumulation | Proteins | Coding | Rodents | Pretreatment | Deactivation | AMP | Mechanical unloading | Unloading | Gene expression | Nuclear transport | Skeletal muscle | Musculoskeletal system | Isoforms | Research Paper | Muscle
AMPK | AICAR | MyHC | hindlimb unloading | soleus muscle | HDAC | HDAC4 | ADAPTIVE RESPONSES | PHYSIOLOGY | ACTIVATED PROTEIN-KINASE | STIMULATION | ATROPHY | PHOSPHORYLATION | TRANSCRIPTION | NEUROSCIENCES | TWITCH MUSCLE | SKELETAL-MUSCLE FIBERS | PLASTICITY | Protein Kinases - metabolism | Phosphorylation | Rats, Wistar | RNA, Messenger - genetics | Myosin Heavy Chains - genetics | Rats | Histone Deacetylases - metabolism | Male | Muscle Fibers, Skeletal - metabolism | RNA, Messenger - metabolism | Myosin Heavy Chains - metabolism | Animals | Cell Nucleus - metabolism | Hindlimb Suspension - adverse effects | Protein Processing, Post-Translational | Active Transport, Cell Nucleus | Muscles | Messenger RNA | T cells | Muscle proteins | Protein kinases | Myosin | Histone deacetylase | Transformation | Calcineurin | Genes | Gene regulation | Chains | Activation | Dephosphorylation | Soleus muscle | Kinases | AMP-activated protein kinase | Nuclei | Accumulation | Proteins | Coding | Rodents | Pretreatment | Deactivation | AMP | Mechanical unloading | Unloading | Gene expression | Nuclear transport | Skeletal muscle | Musculoskeletal system | Isoforms | Research Paper | Muscle
Journal Article
Experimental Physiology, ISSN 0958-0670, 04/2018, Volume 103, Issue 4, pp. 545 - 558
New Findings What is the central question of this study? Translocation of nNOSμ initiates catabolic signalling via FoxO3a and skeletal muscle atrophy during...
p70S6K | hindlimb unloading | reactive oxygen species | atrophy | mTOR | neuronal nitric oxide synthase | Akt | skeletal muscle | oxidative stress | Muscle Fibers, Fast-Twitch - drug effects | TOR Serine-Threonine Kinases - metabolism | Muscle Fibers, Fast-Twitch - metabolism | Rats, Inbred F344 | Rats | Male | Muscle, Skeletal - metabolism | Muscle Fibers, Slow-Twitch - metabolism | Antioxidants - pharmacology | Muscle Fibers, Slow-Twitch - drug effects | Hindlimb Suspension - physiology | Forkhead Box Protein O3 - metabolism | Catalase - metabolism | Animals | Signal Transduction - drug effects | Muscle, Skeletal - drug effects | Muscle Proteins - metabolism | Oxidative Stress - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Superoxide Dismutase - metabolism | Muscles | Nitration | Superoxide | Muscle proteins | Nitric oxide | Alternative splicing | Oxidative stress | Phosphorylation | Reactive oxygen species | Superoxide dismutase | AKT protein | Dephosphorylation | Cytosol | Fibers | Antioxidants | Atrophy | Signal transduction | Catalase | Proteolysis | Rodents | Myosin | Forkhead protein | FOXO3 protein | Phenotypes | Caveolin | Mechanical unloading | Unloading | Nitric-oxide synthase | Skeletal muscle | Musculoskeletal system
p70S6K | hindlimb unloading | reactive oxygen species | atrophy | mTOR | neuronal nitric oxide synthase | Akt | skeletal muscle | oxidative stress | Muscle Fibers, Fast-Twitch - drug effects | TOR Serine-Threonine Kinases - metabolism | Muscle Fibers, Fast-Twitch - metabolism | Rats, Inbred F344 | Rats | Male | Muscle, Skeletal - metabolism | Muscle Fibers, Slow-Twitch - metabolism | Antioxidants - pharmacology | Muscle Fibers, Slow-Twitch - drug effects | Hindlimb Suspension - physiology | Forkhead Box Protein O3 - metabolism | Catalase - metabolism | Animals | Signal Transduction - drug effects | Muscle, Skeletal - drug effects | Muscle Proteins - metabolism | Oxidative Stress - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Superoxide Dismutase - metabolism | Muscles | Nitration | Superoxide | Muscle proteins | Nitric oxide | Alternative splicing | Oxidative stress | Phosphorylation | Reactive oxygen species | Superoxide dismutase | AKT protein | Dephosphorylation | Cytosol | Fibers | Antioxidants | Atrophy | Signal transduction | Catalase | Proteolysis | Rodents | Myosin | Forkhead protein | FOXO3 protein | Phenotypes | Caveolin | Mechanical unloading | Unloading | Nitric-oxide synthase | Skeletal muscle | Musculoskeletal system
Journal Article
Medicine & Science in Sports & Exercise, ISSN 0195-9131, 07/2019, Volume 51, Issue 7, pp. 1396 - 1403
PURPOSEThis study aimed to investigate the effects of downhill treadmill running on mitochondrial structure/function and expression levels of mitophagy-related...
APOPTOSIS | SPORT SCIENCES | MITOCHONDRIA | MITOPHAGY | AUTOPHAGY MAINTAINS | INDUCTION | BIOMARKERS | DOWNHILL TREADMILL RUNNING | PARKIN | PINK1 | ECCENTRIC EXERCISE | SKELETAL MUSCLE | FISSION | DROSOPHILA-PINK1 | PROMOTES | Running | Genetic aspects | Rats as laboratory animals | Research | Health aspects
APOPTOSIS | SPORT SCIENCES | MITOCHONDRIA | MITOPHAGY | AUTOPHAGY MAINTAINS | INDUCTION | BIOMARKERS | DOWNHILL TREADMILL RUNNING | PARKIN | PINK1 | ECCENTRIC EXERCISE | SKELETAL MUSCLE | FISSION | DROSOPHILA-PINK1 | PROMOTES | Running | Genetic aspects | Rats as laboratory animals | Research | Health aspects
Journal Article
Nutrition Research, ISSN 0271-5317, 2012, Volume 32, Issue 2, pp. 144 - 151
Abstract Animal models of type 2 diabetes exhibit reduced peroxisome proliferator–activated receptor- γ coactivator-1 α (PGC-1 α ) messenger RNA (mRNA) levels,...
Gastroenterology and Hepatology | Obesity | Muscle oxidative enzyme activity | Skeletal muscle | Muscle fiber type | PLANTARIS MUSCLES | PGC-1-ALPHA | MODEL | NUTRITION & DIETETICS | INSULIN-RESISTANCE | GLUCOSE | FIBER-TYPE | ADIPOSITY | HYPERTENSIVE KOLETSKY RAT | EXPRESSION | RNA-Binding Proteins - genetics | Cholesterol - blood | Body Weight - drug effects | Diet, High-Fat - adverse effects | Male | Metabolic Syndrome - metabolism | Muscle, Skeletal - metabolism | Sedentary Lifestyle | Insulin - blood | PPAR gamma - metabolism | RNA, Messenger - metabolism | Rats, Inbred Strains | Metabolic Syndrome - blood | Leptin - blood | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Diabetes Mellitus, Type 2 - etiology | Blood Pressure - drug effects | Dietary Fats - adverse effects | Oxidation-Reduction | Rats | Energy Intake - drug effects | Transcription Factors - genetics | Transcription Factors - metabolism | Animals | Metabolic Syndrome - genetics | Triglycerides - blood | Succinate Dehydrogenase - metabolism | Blood Glucose - metabolism | RNA-Binding Proteins - metabolism
Gastroenterology and Hepatology | Obesity | Muscle oxidative enzyme activity | Skeletal muscle | Muscle fiber type | PLANTARIS MUSCLES | PGC-1-ALPHA | MODEL | NUTRITION & DIETETICS | INSULIN-RESISTANCE | GLUCOSE | FIBER-TYPE | ADIPOSITY | HYPERTENSIVE KOLETSKY RAT | EXPRESSION | RNA-Binding Proteins - genetics | Cholesterol - blood | Body Weight - drug effects | Diet, High-Fat - adverse effects | Male | Metabolic Syndrome - metabolism | Muscle, Skeletal - metabolism | Sedentary Lifestyle | Insulin - blood | PPAR gamma - metabolism | RNA, Messenger - metabolism | Rats, Inbred Strains | Metabolic Syndrome - blood | Leptin - blood | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Diabetes Mellitus, Type 2 - etiology | Blood Pressure - drug effects | Dietary Fats - adverse effects | Oxidation-Reduction | Rats | Energy Intake - drug effects | Transcription Factors - genetics | Transcription Factors - metabolism | Animals | Metabolic Syndrome - genetics | Triglycerides - blood | Succinate Dehydrogenase - metabolism | Blood Glucose - metabolism | RNA-Binding Proteins - metabolism
Journal Article
Journal of Surgical Research, ISSN 0022-4804, 2013, Volume 185, Issue 2, pp. 883 - 888
Abstract Purpose Postoperative hypocalcemia is a frequently encountered complication of thyroid surgery. Since hypocalcemic symptoms are closely associated...
Surgery | Testosterone | Soleus | Gender | Estradiol | Skeletal muscle | Hypocalcemia | CALCIUM REGULATORY PROTEINS | SURGERY | CONTRACTILITY | MESSENGER-RNA LEVELS | FEMALE | SKELETAL-MUSCLE | IMPACT | CA2 | TOTAL THYROIDECTOMY | Estradiol - blood | Estrogens - pharmacology | Estrogens - deficiency | Hypocalcemia - metabolism | Androgens - deficiency | Postoperative Complications - metabolism | Male | Testosterone - pharmacology | Estrogens - blood | Androgens - blood | Testosterone - deficiency | Female | Testosterone - blood | Estradiol - pharmacology | Hypocalcemia - etiology | Ovariectomy | Rats | Estradiol - deficiency | Muscle, Skeletal - physiology | Rats, Sprague-Dawley | Thyroidectomy - adverse effects | Orchiectomy | Animals | Androgens - pharmacology | Muscle Contraction - physiology | Sex Factors | Hormones, Sex
Surgery | Testosterone | Soleus | Gender | Estradiol | Skeletal muscle | Hypocalcemia | CALCIUM REGULATORY PROTEINS | SURGERY | CONTRACTILITY | MESSENGER-RNA LEVELS | FEMALE | SKELETAL-MUSCLE | IMPACT | CA2 | TOTAL THYROIDECTOMY | Estradiol - blood | Estrogens - pharmacology | Estrogens - deficiency | Hypocalcemia - metabolism | Androgens - deficiency | Postoperative Complications - metabolism | Male | Testosterone - pharmacology | Estrogens - blood | Androgens - blood | Testosterone - deficiency | Female | Testosterone - blood | Estradiol - pharmacology | Hypocalcemia - etiology | Ovariectomy | Rats | Estradiol - deficiency | Muscle, Skeletal - physiology | Rats, Sprague-Dawley | Thyroidectomy - adverse effects | Orchiectomy | Animals | Androgens - pharmacology | Muscle Contraction - physiology | Sex Factors | Hormones, Sex
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 05/2015, Volume 308, Issue 10, pp. C848 - C855
Effects of macrophage on the responses of soleus fiber size to hind limb unloading and reloading were studied in osteopetrotic homozygous (op/op) mice with...
Satellite cells | Myonuclei | Osteopetrotic mice | Unloading and reloading | Muscle fiber size | muscle fiber size | RAT SOLEUS | PHYSIOLOGY | COLONY-STIMULATING FACTOR | OP OP MOUSE | REGENERATION | myonuclei | CELL BIOLOGY | SKELETAL-MUSCLE | HINDLIMB SUSPENSION | IN-VIVO | GROWTH | osteopetrotic mice | unloading and reloading | DIFFERENTIATION | BED REST | satellite cells | Hypertrophy - prevention & control | Macrophages - pathology | Muscular Atrophy - metabolism | Male | Muscle, Skeletal - metabolism | Osteopetrosis - metabolism | Satellite Cells, Skeletal Muscle - metabolism | Hypertrophy - metabolism | Myoblasts - metabolism | Animals | Muscle Fibers, Skeletal - pathology | Mice | Disease Models, Animal | Physiological aspects | Immune response | Osteopetrosis | Macrophages | Properties
Satellite cells | Myonuclei | Osteopetrotic mice | Unloading and reloading | Muscle fiber size | muscle fiber size | RAT SOLEUS | PHYSIOLOGY | COLONY-STIMULATING FACTOR | OP OP MOUSE | REGENERATION | myonuclei | CELL BIOLOGY | SKELETAL-MUSCLE | HINDLIMB SUSPENSION | IN-VIVO | GROWTH | osteopetrotic mice | unloading and reloading | DIFFERENTIATION | BED REST | satellite cells | Hypertrophy - prevention & control | Macrophages - pathology | Muscular Atrophy - metabolism | Male | Muscle, Skeletal - metabolism | Osteopetrosis - metabolism | Satellite Cells, Skeletal Muscle - metabolism | Hypertrophy - metabolism | Myoblasts - metabolism | Animals | Muscle Fibers, Skeletal - pathology | Mice | Disease Models, Animal | Physiological aspects | Immune response | Osteopetrosis | Macrophages | Properties
Journal Article
Comparisons on the Proportion of Type I and II Fibers in Soleus Muscle and the Visceral Indexes in Rats and Mice, 12/2005
According to age and sex,32 rats and 32 mice were divided into 8 groups. The activities of mATPase of soleus muscle were detected by the mATPase method. Then...
Soleus | Rat | Mouse | Visceral index | Myosine ATPase
Soleus | Rat | Mouse | Visceral index | Myosine ATPase
Journal
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, p. e0169314
Microgravity exposure as well as chronic disuse are two main causes of skeletal muscle atrophy in animals and humans. The antigravity calf soleus is a...
MICROGRAVITY | SKELETAL-MUSCLE | FIBERS | SIGNALING PATHWAYS | ATROPHY | PGC-1 COACTIVATORS | MULTIDISCIPLINARY SCIENCES | MOUSE | RATS | SPACEFLIGHT | BED REST | Muscular Atrophy - metabolism | Mice, Inbred C57BL | Male | Muscle, Skeletal - metabolism | Muscular Atrophy - genetics | Gene Expression Profiling | Muscle Fibers, Slow-Twitch - metabolism | Space Flight | Animals | Time Factors | Microarray Analysis | Weightlessness - adverse effects | Mice | Muscular Atrophy - etiology | Muscles | Gene expression | Microgravity | Analysis | Oxidative stress | Neurosciences | Calcium | Oxidative metabolism | Genes | Homeostasis | Cages | Soleus muscle | Kinases | Machinery | Optimization | Posture | Machinery and equipment | Atrophy | Rodents | Calcium homeostasis | Aerospace medicine | Contractility | Rats | Inflammation | Space flight | Metabolism | Muscle contraction | Biological activity | Skeletal muscle | Ground based control | Studies | Biomarkers | Antigravity | Rehabilitation | Cellular stress response
MICROGRAVITY | SKELETAL-MUSCLE | FIBERS | SIGNALING PATHWAYS | ATROPHY | PGC-1 COACTIVATORS | MULTIDISCIPLINARY SCIENCES | MOUSE | RATS | SPACEFLIGHT | BED REST | Muscular Atrophy - metabolism | Mice, Inbred C57BL | Male | Muscle, Skeletal - metabolism | Muscular Atrophy - genetics | Gene Expression Profiling | Muscle Fibers, Slow-Twitch - metabolism | Space Flight | Animals | Time Factors | Microarray Analysis | Weightlessness - adverse effects | Mice | Muscular Atrophy - etiology | Muscles | Gene expression | Microgravity | Analysis | Oxidative stress | Neurosciences | Calcium | Oxidative metabolism | Genes | Homeostasis | Cages | Soleus muscle | Kinases | Machinery | Optimization | Posture | Machinery and equipment | Atrophy | Rodents | Calcium homeostasis | Aerospace medicine | Contractility | Rats | Inflammation | Space flight | Metabolism | Muscle contraction | Biological activity | Skeletal muscle | Ground based control | Studies | Biomarkers | Antigravity | Rehabilitation | Cellular stress response
Journal Article
Muscle & Nerve, ISSN 0148-639X, 03/2017, Volume 55, Issue 3, pp. 393 - 399
ABSTRACT Introduction: The purpose of our study was to assess the contribution of insulin growth factor‐1–dependent and phosphatidic acid‐dependent signaling...
p70S6K | GSK‐3β | disuse atrophy | reloading | protein synthesis | Akt | soleus muscle | GSK-3β | MAMMALIAN TARGET | PHOSPHORYLATION | ATROPHY | GLYCOGEN-SYNTHASE KINASE-3 | RATS | GSK-3 | NEUROSCIENCES | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | HYPERTROPHY | INHIBITION | PHOSPHATIDIC-ACID | MECHANICAL ACTIVATION | Rats, Wistar | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Protein Biosynthesis - physiology | Phosphodiesterase Inhibitors - pharmacology | Rats | Muscle, Skeletal - physiology | Hindlimb Suspension - physiology | Organ Size - drug effects | Animals | Androstadienes - pharmacology | Signal Transduction - drug effects | Time Factors | Muscle, Skeletal - drug effects | Puromycin - pharmacology | Protein Biosynthesis - drug effects | Signal Transduction - physiology | Protein Synthesis Inhibitors - pharmacology | 1-Butanol - pharmacology | Oncogene Protein v-akt - metabolism | Insulin-Like Growth Factor I - metabolism | Protein biosynthesis | Proteins | Kinases | Protein synthesis | Rodents
p70S6K | GSK‐3β | disuse atrophy | reloading | protein synthesis | Akt | soleus muscle | GSK-3β | MAMMALIAN TARGET | PHOSPHORYLATION | ATROPHY | GLYCOGEN-SYNTHASE KINASE-3 | RATS | GSK-3 | NEUROSCIENCES | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | HYPERTROPHY | INHIBITION | PHOSPHATIDIC-ACID | MECHANICAL ACTIVATION | Rats, Wistar | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Protein Biosynthesis - physiology | Phosphodiesterase Inhibitors - pharmacology | Rats | Muscle, Skeletal - physiology | Hindlimb Suspension - physiology | Organ Size - drug effects | Animals | Androstadienes - pharmacology | Signal Transduction - drug effects | Time Factors | Muscle, Skeletal - drug effects | Puromycin - pharmacology | Protein Biosynthesis - drug effects | Signal Transduction - physiology | Protein Synthesis Inhibitors - pharmacology | 1-Butanol - pharmacology | Oncogene Protein v-akt - metabolism | Insulin-Like Growth Factor I - metabolism | Protein biosynthesis | Proteins | Kinases | Protein synthesis | Rodents
Journal Article
Muscle & Nerve, ISSN 0148-639X, 06/2010, Volume 41, Issue 6, pp. 819 - 827
We investigated the utility of branched‐chain amino acids (BCAA) in dexamethasone‐induced muscle atrophy. Dexamethasone (600 μg/kg, intraperitoneally) and/or...
dexamethasone | atrogin‐1 | autophagy | muscle atrophy | BCAA | Muscle atrophy | Dexamethasone | Atrogin-1 | Autophagy | atrogin-1 | SLOW | PROTEOLYSIS | POSTABSORPTIVE RATS | UBIQUITIN LIGASES | NEUROSCIENCES | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | IN-VIVO | FIBER-TYPE | GENE-EXPRESSION | LEUCINE | Amino Acids, Branched-Chain - therapeutic use | Dexamethasone - administration & dosage | RNA, Messenger - isolation & purification | Body Size | SKP Cullin F-Box Protein Ligases - genetics | RNA, Messenger - genetics | Injections, Intraperitoneal | Organ Size | Rats | Dexamethasone - adverse effects | Male | Glyceraldehyde-3-Phosphate Dehydrogenases - genetics | Muscular Atrophy - chemically induced | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Tripartite Motif Proteins | Muscle Proteins - genetics | Animals | Muscle, Skeletal - drug effects | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Ubiquitin-Protein Ligases - genetics | Muscle, Skeletal - anatomy & histology
dexamethasone | atrogin‐1 | autophagy | muscle atrophy | BCAA | Muscle atrophy | Dexamethasone | Atrogin-1 | Autophagy | atrogin-1 | SLOW | PROTEOLYSIS | POSTABSORPTIVE RATS | UBIQUITIN LIGASES | NEUROSCIENCES | CLINICAL NEUROLOGY | SKELETAL-MUSCLE | IN-VIVO | FIBER-TYPE | GENE-EXPRESSION | LEUCINE | Amino Acids, Branched-Chain - therapeutic use | Dexamethasone - administration & dosage | RNA, Messenger - isolation & purification | Body Size | SKP Cullin F-Box Protein Ligases - genetics | RNA, Messenger - genetics | Injections, Intraperitoneal | Organ Size | Rats | Dexamethasone - adverse effects | Male | Glyceraldehyde-3-Phosphate Dehydrogenases - genetics | Muscular Atrophy - chemically induced | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Tripartite Motif Proteins | Muscle Proteins - genetics | Animals | Muscle, Skeletal - drug effects | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Ubiquitin-Protein Ligases - genetics | Muscle, Skeletal - anatomy & histology
Journal Article
Scandinavian Journal of Medicine and Science in Sports, ISSN 0905-7188, 03/2018, Volume 28, Issue 3, pp. 1009 - 1017
Achilles tendon (AT) comprises of 3 subtendons arising from the soleus (SOL) and the lateral (LG) and medial (MG) heads of the gastrocnemius muscle. While...
triceps surae | ankle torque | Orthopedics and Sports Medicine | anatomy | Achilles tendon | deformation | 3-dimensional model | Physical Therapy, Sports Therapy and Rehabilitation | 3‐dimensional model | SPORT SCIENCES | WALKING | LENGTH | PATTERNS | ENERGY-STORING TENDONS | FORCE TRANSMISSION | FASCICLES | IN-VIVO | MUSCLES | Torque | Animals | Muscle Contraction | Ankle Joint - physiology | Rats, Wistar | Rats | Achilles Tendon - physiology | Male | Muscle, Skeletal - physiology | Achilles Tendon - anatomy & histology | Ankle | Rodents | Sports medicine | Tendons
triceps surae | ankle torque | Orthopedics and Sports Medicine | anatomy | Achilles tendon | deformation | 3-dimensional model | Physical Therapy, Sports Therapy and Rehabilitation | 3‐dimensional model | SPORT SCIENCES | WALKING | LENGTH | PATTERNS | ENERGY-STORING TENDONS | FORCE TRANSMISSION | FASCICLES | IN-VIVO | MUSCLES | Torque | Animals | Muscle Contraction | Ankle Joint - physiology | Rats, Wistar | Rats | Achilles Tendon - physiology | Male | Muscle, Skeletal - physiology | Achilles Tendon - anatomy & histology | Ankle | Rodents | Sports medicine | Tendons
Journal Article
Muscle & Nerve, ISSN 0148-639X, 08/2016, Volume 54, Issue 2, pp. 300 - 307
ABSTRACT Introduction: The potential of gender to affect unloading‐induced neuromuscular adaptations was investigated. Methods: Twenty male and 20 female rats...
unweighting | myofiber | disuse | strength | neuromuscular junction | Unweighting | Myofiber | Neuromuscular junction | Disuse | Strength | LOWER-LIMB SUSPENSION | FATIGUE | HUMANS | NEUROSCIENCES | CLINICAL NEUROLOGY | SPACE | SKELETAL-MUSCLE | RECOVERY | TRANSMISSION | AGED RATS | Torque | Electric Stimulation | Rats, Wistar | Adaptation, Physiological - physiology | Organ Size | Rats | Male | Muscle, Skeletal - physiology | Sex Characteristics | Animals | Muscle Contraction - physiology | Female | Neuromuscular Junction - physiology | Females | Rodents | Gender
unweighting | myofiber | disuse | strength | neuromuscular junction | Unweighting | Myofiber | Neuromuscular junction | Disuse | Strength | LOWER-LIMB SUSPENSION | FATIGUE | HUMANS | NEUROSCIENCES | CLINICAL NEUROLOGY | SPACE | SKELETAL-MUSCLE | RECOVERY | TRANSMISSION | AGED RATS | Torque | Electric Stimulation | Rats, Wistar | Adaptation, Physiological - physiology | Organ Size | Rats | Male | Muscle, Skeletal - physiology | Sex Characteristics | Animals | Muscle Contraction - physiology | Female | Neuromuscular Junction - physiology | Females | Rodents | Gender
Journal Article
Biochemistry and Cell Biology, ISSN 0829-8211, 2016, Volume 94, Issue 2, pp. 101 - 108
We studied whether short-term administration of triiodothyronine (T 3 ) for the last 3 days of endurance training would influence the rate of uptake of...
muscle squelettique | fatty acid uptake | triacylglycerols | triacylglycérols | short-term hyperthyroidism | skeletal muscle | hyperthyroïdie à court terme | captation des acides gras | Fatty acid uptake | Short-term hyperthyroidism | Skeletal muscle | Triacylglycerols | Animals | Rats, Wistar | Muscle, Skeletal - drug effects | Rats | Male | Muscle, Skeletal - metabolism | Physical Endurance | Fatty Acids - metabolism | Physical Conditioning, Animal | Triiodothyronine - administration & dosage | Triiodothyronine - pharmacology | Muscles | Triiodothyronine | Dosage and administration | Fatty acid metabolism | Health aspects
muscle squelettique | fatty acid uptake | triacylglycerols | triacylglycérols | short-term hyperthyroidism | skeletal muscle | hyperthyroïdie à court terme | captation des acides gras | Fatty acid uptake | Short-term hyperthyroidism | Skeletal muscle | Triacylglycerols | Animals | Rats, Wistar | Muscle, Skeletal - drug effects | Rats | Male | Muscle, Skeletal - metabolism | Physical Endurance | Fatty Acids - metabolism | Physical Conditioning, Animal | Triiodothyronine - administration & dosage | Triiodothyronine - pharmacology | Muscles | Triiodothyronine | Dosage and administration | Fatty acid metabolism | Health aspects
Journal Article