overuse of muscle - перевод на русский
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  • частота употребления
  • используется оно чаще в устной или письменной речи
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overuse of muscle - перевод на русский

PROCESS THAT IS CHARACTERIZED BY A DECREASE IN PROTEIN CONTENT, FIBER DIAMETER, FORCE PRODUCTION AND FATIGUE RESISTANCE.
Muscular atrophy; Muscle Atrophy; Muscular disorders, atrophic; Muscle wasting; Muscle wasting and atrophy; Muscular wasting; Loss of muscle; Reduced muscle mass; Loss of muscle mass; Decreased muscle mass
  • Atrophy with paralysis due to [[ankylosis]]
  • Severe muscular atrophy leading to emaciation in a young girl with chronic [[rheumatism]]

overuse of muscle      

медицина

перегрузка мышцы

muscle strength         
  • When a sarcomere contracts, the Z lines move closer together, and the I band becomes smaller. The A band stays the same width. At full contraction, the thin and thick filaments overlap.
  • (a) Some ATP is stored in a resting muscle. As contraction starts, it is used up in seconds. More ATP is generated from creatine phosphate for about 15 seconds. (b) Each glucose molecule produces two ATP and two molecules of pyruvic acid, which can be used in aerobic respiration or converted to [[lactic acid]]. If oxygen is not available, pyruvic acid is converted to lactic acid, which may contribute to [[muscle fatigue]]. This occurs during strenuous exercise when high amounts of energy are needed but oxygen cannot be sufficiently delivered to muscle. (c) Aerobic respiration is the breakdown of glucose in the presence of oxygen (O2) to produce carbon dioxide, water, and ATP. Approximately 95 percent of the ATP required for resting or moderately active muscles is provided by aerobic respiration, which takes place in mitochondria.
  • ATPase staining of a muscle cross section. Type II fibers are dark, due to the alkaline pH of the preparation. In this example, the size of the type II fibers is considerably less than the type I fibers due to denervation atrophy.
  • Types of [[pennate muscle]]. A – [[unipennate]];  B – [[bipennate]]; 
C – [[multipennate]]
  • [[Human embryo]] showing [[somite]]s labelled as ''primitive segments''.
  • polypeptide]] tail (only one tail of each pair is shown). The pairs of histones, H2A, H2B, H3 and H4, each have [[lysine]]s (K) in their tails, some of which are subject to post-translational modifications consisting, usually, of acetylations [Ac] and methylations {me}. The lysines (K) are designated with a number showing their position as, for instance, (K4), indicating lysine as the 4th amino acid from the amino (N) end of the tail in the histone protein. The particular acetylations [Ac] and methylations {Me} shown are those that occur on nucleosomes close to, or at, some DNA regions undergoing transcriptional activation of the DNA wrapped around the nucleosome.
  • Prisoner of war exhibiting muscle loss as a result of [[malnutrition]].
  • [[Jogging]] is one form of aerobic exercise.
  • Muscle types by fiber arrangement
  • Exercise-induced signaling pathways in skeletal muscle that determine specialized characteristics of slow- and fast-twitch muscle fibers
  • In [[muscular dystrophy]], the affected tissues become disorganized and the concentration of [[dystrophin]] (green) is greatly reduced.
  •  
'''Regulation of transcription in mammals.'''  An active enhancer regulatory region is enabled to interact with the promoter region of its target gene by formation of a chromosome loop. This can allow initiation of messenger RNA (mRNA) synthesis by RNA polymerase II (RNAP II) bound to the promoter at the transcription start site of the gene. The loop is stabilized by one architectural protein anchored to the enhancer and one anchored to the promoter, and these proteins are joined together to form a dimer (red zigzags). Specific regulatory transcription factors bind to DNA sequence motifs on the enhancer. General transcription factors bind to the promoter. When a transcription factor is activated by a signal (here indicated as phosphorylation shown by a small red star on a transcription factor on the enhancer) the enhancer is activated and can now activate its target promoter. The active enhancer is transcribed on each strand of DNA in opposite directions by bound RNAP IIs. Mediator (a complex consisting of about 26 proteins in an interacting structure) communicates regulatory signals from the enhancer DNA-bound transcription factors to the promoter.
  • Structure of muscle fibre showing a sarcomere under [[electron microscope]] with schematic explanation.
ONE OF THREE MAJOR MUSCLE TYPES
Skeletal muscles; Voluntary muscle; Musculo; Red skeletal muscle cell; White skeletal muscle cell; Muscle protein; Fast twitch muscle; Slow twitch muscles; Skeletal Muscle; Strongest muscle in human body; Muscle loss; Musculature; Muscle mass; Muscle, skeletal; Muscular branches; Muscle fibers, slow-twitch; Muscular diseases; Myoblasts, skeletal; Control of Muscles; Voluntary muscles; Characteristics of muscle; Muscular fiber; Skeletal muscular; Lean muscle; Muscles; Slow-twitch muscle; Panniculus carnosis; Neoplasms, muscle tissue; Excitation-contraction; Muscle proteins; Muscle strength; Muscle; Myoid cells; Branchialis; Connective tissue in skeletal muscle; Connective tissue of skeletal muscle; Muscle types; Convergent muscles; Human muscle; Fast-twitching; Textus muscularis striatus skeletalis; Skeletal muscle cells; Muscular; Gross anatomy of muscles; Muscular force; Myo-; Skeletal striated muscles; Fast twitch fibre; Slow twitch fibre; Slow twitch fiber; Fast twitch fiber; Skeletal striated muscle; Muscular fibers; Myonuclei; Evolution of muscles; Skeletal muscle fibers; Myotendinous junction; Muscle group; Groups of muscles; Msucle; Musculotendinous junction; Skeletal muscle cell

общая лексика

мышечная сила

voluntary muscle         
  • When a sarcomere contracts, the Z lines move closer together, and the I band becomes smaller. The A band stays the same width. At full contraction, the thin and thick filaments overlap.
  • (a) Some ATP is stored in a resting muscle. As contraction starts, it is used up in seconds. More ATP is generated from creatine phosphate for about 15 seconds. (b) Each glucose molecule produces two ATP and two molecules of pyruvic acid, which can be used in aerobic respiration or converted to [[lactic acid]]. If oxygen is not available, pyruvic acid is converted to lactic acid, which may contribute to [[muscle fatigue]]. This occurs during strenuous exercise when high amounts of energy are needed but oxygen cannot be sufficiently delivered to muscle. (c) Aerobic respiration is the breakdown of glucose in the presence of oxygen (O2) to produce carbon dioxide, water, and ATP. Approximately 95 percent of the ATP required for resting or moderately active muscles is provided by aerobic respiration, which takes place in mitochondria.
  • ATPase staining of a muscle cross section. Type II fibers are dark, due to the alkaline pH of the preparation. In this example, the size of the type II fibers is considerably less than the type I fibers due to denervation atrophy.
  • Types of [[pennate muscle]]. A – [[unipennate]];  B – [[bipennate]]; 
C – [[multipennate]]
  • [[Human embryo]] showing [[somite]]s labelled as ''primitive segments''.
  • polypeptide]] tail (only one tail of each pair is shown). The pairs of histones, H2A, H2B, H3 and H4, each have [[lysine]]s (K) in their tails, some of which are subject to post-translational modifications consisting, usually, of acetylations [Ac] and methylations {me}. The lysines (K) are designated with a number showing their position as, for instance, (K4), indicating lysine as the 4th amino acid from the amino (N) end of the tail in the histone protein. The particular acetylations [Ac] and methylations {Me} shown are those that occur on nucleosomes close to, or at, some DNA regions undergoing transcriptional activation of the DNA wrapped around the nucleosome.
  • Prisoner of war exhibiting muscle loss as a result of [[malnutrition]].
  • [[Jogging]] is one form of aerobic exercise.
  • Muscle types by fiber arrangement
  • Exercise-induced signaling pathways in skeletal muscle that determine specialized characteristics of slow- and fast-twitch muscle fibers
  • In [[muscular dystrophy]], the affected tissues become disorganized and the concentration of [[dystrophin]] (green) is greatly reduced.
  •  
'''Regulation of transcription in mammals.'''  An active enhancer regulatory region is enabled to interact with the promoter region of its target gene by formation of a chromosome loop. This can allow initiation of messenger RNA (mRNA) synthesis by RNA polymerase II (RNAP II) bound to the promoter at the transcription start site of the gene. The loop is stabilized by one architectural protein anchored to the enhancer and one anchored to the promoter, and these proteins are joined together to form a dimer (red zigzags). Specific regulatory transcription factors bind to DNA sequence motifs on the enhancer. General transcription factors bind to the promoter. When a transcription factor is activated by a signal (here indicated as phosphorylation shown by a small red star on a transcription factor on the enhancer) the enhancer is activated and can now activate its target promoter. The active enhancer is transcribed on each strand of DNA in opposite directions by bound RNAP IIs. Mediator (a complex consisting of about 26 proteins in an interacting structure) communicates regulatory signals from the enhancer DNA-bound transcription factors to the promoter.
  • Structure of muscle fibre showing a sarcomere under [[electron microscope]] with schematic explanation.
ONE OF THREE MAJOR MUSCLE TYPES
Skeletal muscles; Voluntary muscle; Musculo; Red skeletal muscle cell; White skeletal muscle cell; Muscle protein; Fast twitch muscle; Slow twitch muscles; Skeletal Muscle; Strongest muscle in human body; Muscle loss; Musculature; Muscle mass; Muscle, skeletal; Muscular branches; Muscle fibers, slow-twitch; Muscular diseases; Myoblasts, skeletal; Control of Muscles; Voluntary muscles; Characteristics of muscle; Muscular fiber; Skeletal muscular; Lean muscle; Muscles; Slow-twitch muscle; Panniculus carnosis; Neoplasms, muscle tissue; Excitation-contraction; Muscle proteins; Muscle strength; Muscle; Myoid cells; Branchialis; Connective tissue in skeletal muscle; Connective tissue of skeletal muscle; Muscle types; Convergent muscles; Human muscle; Fast-twitching; Textus muscularis striatus skeletalis; Skeletal muscle cells; Muscular; Gross anatomy of muscles; Muscular force; Myo-; Skeletal striated muscles; Fast twitch fibre; Slow twitch fibre; Slow twitch fiber; Fast twitch fiber; Skeletal striated muscle; Muscular fibers; Myonuclei; Evolution of muscles; Skeletal muscle fibers; Myotendinous junction; Muscle group; Groups of muscles; Msucle; Musculotendinous junction; Skeletal muscle cell
[анат.] произвольно сокращающаяся мышца

Определение

грип
ГРИП, ГРИПП, гриппа, ·муж. (·франц. grippe) (мед.). Инфекционная болезнь - катарральное воспаление дыхательных путей, сопровождаемое лихорадочным состоянием; то же, что инфлуэнца
.

Википедия

Muscle atrophy

Muscle atrophy is the loss of skeletal muscle mass. It can be caused by immobility, aging, malnutrition, medications, or a wide range of injuries or diseases that impact the musculoskeletal or nervous system. Muscle atrophy leads to muscle weakness and causes disability.

Disuse causes rapid muscle atrophy and often occurs during injury or illness that requires immobilization of a limb or bed rest. Depending on the duration of disuse and the health of the individual, this may be fully reversed with activity. Malnutrition first causes fat loss but may progress to muscle atrophy in prolonged starvation and can be reversed with nutritional therapy. In contrast, cachexia is a wasting syndrome caused by an underlying disease such as cancer that causes dramatic muscle atrophy and cannot be completely reversed with nutritional therapy. Sarcopenia is age-related muscle atrophy and can be slowed by exercise. Finally, diseases of the muscles such as muscular dystrophy or myopathies can cause atrophy, as well as damage to the nervous system such as in spinal cord injury or stroke. Thus, muscle atrophy is usually a finding (sign or symptom) in a disease rather than being a disease by itself. However, some syndromes of muscular atrophy are classified as disease spectrums or disease entities rather than as clinical syndromes alone, such as the various spinal muscular atrophies.

Muscle atrophy results from an imbalance between protein synthesis and protein degradation, although the mechanisms are incompletely understood and are variable depending on the cause. Muscle loss can be quantified with advanced imaging studies but this is not frequently pursued. Treatment depends on the underlying cause but will often include exercise and adequate nutrition. Anabolic agents may have some efficacy but are not often used due to side effects. There are multiple treatments and supplements under investigation but there are currently limited treatment options in clinical practice. Given the implications of muscle atrophy and limited treatment options, minimizing immobility is critical in injury or illness.

Как переводится overuse of muscle на Русский язык