Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Muscles, skeletal

Skeletal muscle (Fig. 12.1) consists of long, thin, parallel cells arranged into fiber bundles. Each of these muscle fibers exists as a separate entity surrounded by connective tissue, the endomysium. Numbers of these primary muscle [Pg.564]

Country Chicken meat Country Duck meat Country Meat, grand total [Pg.565]

Year Beef/Veal Pork Poultry Total [Pg.565]

The membrane surrounding each individual muscle fiber is called the sarcolemma (thickness ca. 75 nm). It consists of three layers the endomysium, a middle amorphous layer and an inner plasma membrane. Muscle fibers are polynuclear cells. The nuclei are surrounded by the sarcoplasm and by other cellular elements (mitochondria, sarcoplasmic reticulum, lyso- [Pg.565]

Country/ region Year Beef/ Veal Pork Poultry Total [Pg.565]

Quinine, quinidine, cinchonine, and cinchonidine have similar actions. Dilute solutions cause direct depression with prolonged refractory phase. Concentrated solutions produce rigor. [Pg.252]


HisN03,(CH3)3N + -CH2 CH0H CH2C00-. Isolated from skeletal muscle. It acts as a carrier for ethanoyl groups and fatty acyl groups across the mitochondrial membrane during the biosynthesis or oxidation of fatty acids. [Pg.84]

C14H30CI2N2O4. White powder prepared from dimethylaminoethanol and succinyl chloride, followed by methylation. Neuromuscular blocking agent used to relax skeletal muscles during certain types of surgical operation. [Pg.382]

The growth of animals can be defined as an increase in mass of whole body, tissue(s), organ(s), or ceU(s) with time. This type of growth can be characterized by morphometric measurements eg, skeletal muscle or adipose tissue growth can be described by observing temporal changes in ceU number, ie, hyperplasia, and ceU size, ie, hypertrophy. Growth also includes developmental aspects of function and metaboHsm of cells and tissues from conception to maturity. [Pg.408]

One possible mechanism responsible for the abiHty of trenbolone acetate to stimulate skeletal muscle hypertrophy may be through enhanced proliferation and differentiation of satelHte ceUs as the result of increased sensitivity to insuHn-Hke growth factor-I (IGE-1) and fibroblast growth factor (43). [Pg.409]

Data for carcass composition corresponding to protein and lipid are percent-dissected skeletal muscle and adipose, respectively. [Pg.414]

Mechanism of Action. P-Agonists stimulate skeletal muscle growth by accelerating rates of fiber hypertrophy and protein synthesis, but generally do not alter muscle DNA content in parallel with the increases in protein accretion (133—135). This is in contrast to the effects of anaboHc steroids and ST on skeletal muscle growth. Both of the latter stimulate fiber hypertrophy and muscle protein synthesis, but also increase muscle DNA content coincident with increased protein accretion. Whether the P-agonists decrease muscle protein degradation is equivocal. [Pg.414]

The absorption of sulfonylureas from the upper gastrointestinal tract is faidy rapid and complete. The agents are transported in the blood as protein-bound complexes. As they are released from protein-binding sites, the free (unbound) form becomes available for diffusion into tissues and to sites of action. Specific receptors are present on pancreatic islet P-ceU surfaces which bind sulfonylureas with high affinity. Binding of sulfonylureas to these receptors appears to be coupled to an ATP-sensitive channel to stimulate insulin secretion. These agents may also potentiate insulin-stimulated glucose transport in adipose tissue and skeletal muscle. [Pg.341]

The sacroplasmic proteins myoglobin and hemoglobin are responsible for much of the color in meat. Species vary tremendously in the amount of sacroplasmic proteins within skeletal muscle with catde, sheep, pigs, and poultry Hsted in declining order of sarcoplasmic protein content. Fat is also an important component of meat products. The amount of fat in a portion of meat varies depending on the species, anatomy, and state of nutrition of the animal. The properties of processed meat products are greatiy dependent on the properties of the fat included. Certain species, such as sheep, have a relatively higher proportion of saturated fat, whereas other species, such as poultry, have a relatively lower proportion of saturated fat. It is well known that the characteristic davors of meat from different species are in part determined by their fat composition. [Pg.32]

Autoantibodies are directed against nicotinic acetylcholine receptors in myasthenia gravis, resulting in receptor loss, skeletal muscle paralysis, and dysfunction (100). In addition, antibodies directed against voltage-gated Ca " channels produce similar neuromuscular dysfunction of Lambert-Eaton... [Pg.282]

Historical Inhalation Agents. Diethyl ether produces excellent surgical anesthesia, but it is flammable (see Ethers). Chloroform is a nonflammable, sweet smelling, colorless Hquid which provides analgesia at nonanesthetic doses and can provide potent anesthesia at 1% (see Chlorocarbons AND CHLOROHYDROCARBONs). However, a metabohte causes hepatic cell necrosis. Tdlene, a nonflammable colorless Hquid, has a slower onset and recovery and a higher toxicity and chemical reactivity than desirable. Cyclopropane is a colorless gas which has rapid induction (2 —3 min) and recovery characteristics and analgesia is obtained in the range of 3—5% with adequate skeletal muscle relaxation (see Hydrocarbons). The use of cyclopropane has ceased, however, because of its flammabiHty and marked predisposition to cause arrhythmias. [Pg.408]

Florfenicol concentrations in tissues and body fluids of male veal calves were studied after 11 mg/kg intramuscular doses adininistered at 12-h intervals (42). Concentrations of florfenicol in the lungs, heart, skeletal muscle, synovia, spleen, pancreas, large intestine, and small intestine were similar to the corresponding semm concentrations indicating excellent penetration of florfenicol into these tissues. Because the florfenicol concentration in these tissues decreased over time as did the corresponding semm concentrations, it was deemed that florfenicol equiUbrated rapidly between these tissues and the blood. Thus semm concentrations of florfenicol can be used as an indicator of dmg concentrations in these tissues. [Pg.517]

Muscle tissue is unique in its ability to shorten or contract. The human body has three basic types of muscle tissue histologically classified into smooth, striated, and cardiac muscle tissues. Only the striated muscle tissue is found in all skeletal muscles. The type of cells which compose the muscle tissue are known as contractile cells. They originate from mesenchymal cells which differentiate into myoblasts. Myoblasts are embryonic cells which later differentiate into contractile fiber cells. [Pg.185]

Proteins can be broadly classified into fibrous and globular. Many fibrous proteins serve a stmctural role (11). CC-Keratin has been described. Fibroin, the primary protein in silk, has -sheets packed one on top of another. CoUagen, found in connective tissue, has a triple-hehcal stmcture. Other fibrous proteins have a motile function. Skeletal muscle fibers are made up of thick filaments consisting of the protein myosin, and thin filaments consisting of actin, troponin, and tropomyosin. Muscle contraction is achieved when these filaments sHde past each other. Microtubules and flagellin are proteins responsible for the motion of ciUa and bacterial dageUa. [Pg.211]

Health and Safety Factors. Clinical side effects and LD q values of most commercially available analeptics have been summarized (2). Overdoses produce symptoms of extreme CNS excitation, including resdessness, hyperexcitabiUty, skeletal muscle hyperactivity, and ia some cases convulsions. [Pg.463]

In the tissues of animals, most thiamine is found as its phosphorylated esteis (4—6) and is piedominandy bound to enzymes as the pyrophosphate (5), the active coen2yme form. As expected for a factor involved in carbohydrate metaboHsm, the highest concentrations ate generally found in organs with high activity, such as the heart, kidney, Hver, and brain. In humans this typically amounts to 1—8 p.g/g of wet tissue, with lesser amounts in the skeletal muscles (35). A typical healthy human body may contain about 30 mg of thiamine in all forms, about 40—50% of this being in the muscles owing to their bulk. Almost no excess is stored. Normal human blood contains about 90 ng/mL, mostly in the ted cells and leukocytes. A value below 40 ng/mL is considered indicative of a possible deficiency. Amounts and proportions in the tissues of other animal species vary widely (31,35). [Pg.88]

P-Adrenoceptors have been subdivided into P - and P2-adrenoceptors. A third subset called nontypical P-adrenoceptors or P -adrenoceptors have been described but are stiU the subject of debate. In terms of the interactions with various subsets of P-adrenoceptors, some antagonists are nonselective in that they antagonize the effects of activation of both P - and P2-adrenoceptors, whereas others are selective for either P - or P2-adrenoceptors. P - and P2-adrenoceptors coexist in almost all organs but generally, one type predominates. The focus herein is on the clinically relevant P -adrenoceptor-mediated effects on heart and on P2-adrenoceptor-mediated effects on smooth muscles of blood vessels and bronchioles, the insulin-secreting tissue of the pancreas, and skeletal muscle glycogenolysis for side effects profile (36). [Pg.114]

Sygusch, J., Beaudry, D., Allaire, M. Molecular architecture of rabbit skeletal muscle aldolase at 2.7 A resolution. Proe. Natl. Aead. Sei. USA 84 ... [Pg.65]


See other pages where Muscles, skeletal is mentioned: [Pg.65]    [Pg.541]    [Pg.408]    [Pg.411]    [Pg.412]    [Pg.413]    [Pg.413]    [Pg.413]    [Pg.413]    [Pg.414]    [Pg.414]    [Pg.169]    [Pg.169]    [Pg.243]    [Pg.515]    [Pg.515]    [Pg.516]    [Pg.268]    [Pg.269]    [Pg.407]    [Pg.445]    [Pg.215]    [Pg.301]    [Pg.301]    [Pg.126]    [Pg.573]    [Pg.370]    [Pg.207]    [Pg.362]    [Pg.714]    [Pg.723]    [Pg.778]    [Pg.229]    [Pg.533]   
See also in sourсe #XX -- [ Pg.556 , Pg.568 ]

See also in sourсe #XX -- [ Pg.230 ]

See also in sourсe #XX -- [ Pg.9 ]

See also in sourсe #XX -- [ Pg.62 , Pg.258 , Pg.259 , Pg.263 , Pg.264 , Pg.265 , Pg.268 , Pg.269 , Pg.270 , Pg.271 , Pg.272 , Pg.273 , Pg.274 , Pg.275 , Pg.276 ]

See also in sourсe #XX -- [ Pg.20 ]

See also in sourсe #XX -- [ Pg.104 ]

See also in sourсe #XX -- [ Pg.17 ]

See also in sourсe #XX -- [ Pg.7 , Pg.9 , Pg.11 , Pg.67 , Pg.74 , Pg.126 , Pg.244 , Pg.254 , Pg.299 ]

See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.121 , Pg.129 ]

See also in sourсe #XX -- [ Pg.325 ]

See also in sourсe #XX -- [ Pg.121 ]

See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.177 ]

See also in sourсe #XX -- [ Pg.517 ]

See also in sourсe #XX -- [ Pg.235 , Pg.337 , Pg.339 , Pg.454 , Pg.455 , Pg.488 , Pg.787 ]

See also in sourсe #XX -- [ Pg.370 , Pg.373 ]

See also in sourсe #XX -- [ Pg.43 , Pg.44 ]

See also in sourсe #XX -- [ Pg.456 ]

See also in sourсe #XX -- [ Pg.14 , Pg.410 , Pg.415 ]

See also in sourсe #XX -- [ Pg.14 , Pg.30 , Pg.35 , Pg.79 , Pg.83 , Pg.103 , Pg.106 , Pg.108 , Pg.110 , Pg.111 , Pg.114 , Pg.116 , Pg.118 , Pg.122 , Pg.123 , Pg.124 ]

See also in sourсe #XX -- [ Pg.73 ]

See also in sourсe #XX -- [ Pg.491 ]

See also in sourсe #XX -- [ Pg.201 ]

See also in sourсe #XX -- [ Pg.564 , Pg.566 , Pg.567 ]

See also in sourсe #XX -- [ Pg.580 , Pg.680 , Pg.695 ]




SEARCH



ATPases skeletal muscle

Acetylcholine receptors in skeletal muscle

Acetylcholine receptors skeletal muscle

Acetylcholine skeletal muscle

Acetylcholinesterase in skeletal muscle

Actin based regulation (skeletal and cardiac muscle)

Actin skeletal muscle

Adverse drug reactions muscle, skeletal

Androgen skeletal muscle

Baclofen, a skeletal muscle relaxant, acts at the spinal cord level to inhibit transmission of monosynaptic and polysynaptic reflexes

Biochemical adaptations, skeletal muscle

Biomarkers skeletal muscle injury, drug-induced

Botulinum toxin causes skeletal muscle paralysis by binding to acetylcholine receptors on the motor end plate

Browning skeletal muscle

Chicken skeletal muscle, comparison

Corticosteroids skeletal muscle effects

Curare skeletal muscle relaxants

Drug-induced skeletal muscle injury

Drugs depressing skeletal muscle relaxants

Enzyme skeletal muscle, release

Enzymes skeletal muscles

Fast-twitch skeletal muscle

Fenofibrate skeletal muscle

Fiber types in skeletal muscle

Fuel utilization skeletal muscle

Glucose in skeletal muscle

Glucose transporter skeletal muscle

Heart and Skeletal Muscle

Human skeletal muscle Na+ channels

Human skeletal muscle, comparison

INDEX skeletal muscles, enzymes

Imaging skeletal muscle

Immune system skeletal muscle

In skeletal muscle

Insulin resistance, skeletal muscle

Lean skeletal muscle tissue

Length-tension relationship skeletal muscle

Muscle cells, skeletal, translocation

Muscle contractile proteins, skeletal

Muscle skeletal, crossbridges

Muscle skeletal, lactate dehydrogenase

Muscle skeletal, micrograph

Muscle skeletal, myofibrillar proteins

Muscle, skeletal NSAIDS

Muscle, skeletal intramuscular drug administration

Muscle, skeletal myopathy

Muscle, skeletal neuromuscular blockers

Muscle, skeletal rhabdomyolysis

Muscle, skeletal tranquillizers

Muscle, skeletal transferase

Muscle-cell surface skeletal

Muscles, skeletal electrophysiology

Muscles, skeletal smooth

Neuromuscular blocking agents skeletal muscle effects

Novel Translational Biomarkers of Skeletal Muscle Injury

Of Rabbit Skeletal Muscle

Oxidative stress skeletal muscle

Protein in skeletal muscle

Quinine skeletal muscle

ROS production in chicken skeletal muscle under acute heat stress conditions

Rabbit skeletal muscle

Relaxation of the skeletal muscl

Sarcoplasmic reticulum skeletal muscle

Signal patterns in proton spectra of skeletal muscle

Skeletal Muscle Can Function Aerobically or Anaerobically

Skeletal Muscle Tumors

Skeletal Muscle and Peripheral Nerve Pathology

Skeletal muscle INDEX

Skeletal muscle Na+ channels

Skeletal muscle acetylcholine release

Skeletal muscle arteries

Skeletal muscle autonomic regulation

Skeletal muscle caffeine, effects

Skeletal muscle calcium

Skeletal muscle calcium movement

Skeletal muscle calcium pump

Skeletal muscle cells

Skeletal muscle changes

Skeletal muscle changes function

Skeletal muscle changes neuromuscular junction

Skeletal muscle changes structure

Skeletal muscle changes units

Skeletal muscle cholinergic system

Skeletal muscle cholinergic transmission

Skeletal muscle connectin

Skeletal muscle contractile activity

Skeletal muscle contractions

Skeletal muscle creatine kinase

Skeletal muscle cytoskeletal proteins

Skeletal muscle description

Skeletal muscle diseases

Skeletal muscle disorders

Skeletal muscle drugs causing relaxation

Skeletal muscle dysfunction

Skeletal muscle effects

Skeletal muscle excitation-contraction coupling

Skeletal muscle fatigue

Skeletal muscle fiber types

Skeletal muscle fibers, fatigue

Skeletal muscle fuels

Skeletal muscle functions

Skeletal muscle glycogen

Skeletal muscle glycogen stores

Skeletal muscle glycogenolysis

Skeletal muscle heat production

Skeletal muscle innervation

Skeletal muscle isometric

Skeletal muscle isotonic

Skeletal muscle lactic dehydrogenase

Skeletal muscle localization

Skeletal muscle mechanics

Skeletal muscle mechanisms

Skeletal muscle metabolism

Skeletal muscle metabolism nucleotides

Skeletal muscle mitochondrial content

Skeletal muscle motor end plate

Skeletal muscle movement

Skeletal muscle neuromuscular blockade

Skeletal muscle neuromuscular junction

Skeletal muscle nicotinic receptors

Skeletal muscle oxidative capacity

Skeletal muscle phosphates

Skeletal muscle phosphorus

Skeletal muscle phosphorylase deficiency

Skeletal muscle protein

Skeletal muscle pump

Skeletal muscle quantitative analysis

Skeletal muscle regeneration process

Skeletal muscle regulatory proteins

Skeletal muscle relaxant

Skeletal muscle relaxant chlorzoxazone

Skeletal muscle relaxant drugs

Skeletal muscle relaxant drugs spasms

Skeletal muscle relaxants baclofen

Skeletal muscle relaxants centrally acting

Skeletal muscle relaxants depolarizing

Skeletal muscle relaxants neuromuscular blocking drugs

Skeletal muscle relaxants nondepolarizing

Skeletal muscle relaxants sedative-hypnotics

Skeletal muscle respiratory capacity

Skeletal muscle sarcomeres

Skeletal muscle slow twitch fibers

Skeletal muscle spasm

Skeletal muscle specificity

Skeletal muscle strength

Skeletal muscle structure

Skeletal muscle structure development

Skeletal muscle system

Skeletal muscle system neuromuscular reflexes

Skeletal muscle thick filaments

Skeletal muscle thin filaments

Skeletal muscle thyroid hormones

Skeletal muscle tissue

Skeletal muscle tissue clinical application

Skeletal muscle tissue engineering

Skeletal muscle tolerance development

Skeletal muscle transaminase activities

Skeletal muscle tropomyosin

Skeletal muscle troponin

Skeletal muscle xanthine effects

Skeletal muscles AChE activity

Skeletal muscles BuChE activity

Skeletal muscles cholinergic toxicity

Skeletal muscles experimental model

Skeletal muscles hypoxic response

Skeletal muscles muscle development

Skeletal muscles muscle excitotoxicity

Skeletal muscles muscle fibers

Skeletal muscles necrotic fibers

Skeletal muscles neonatal

Skeletal muscles postnatal

Slow-twitch skeletal muscle

Soman skeletal muscle effects

Stimulants, skeletal muscle

Striated skeletal muscle

Structure and Development of Skeletal Muscle

Structure of skeletal muscle

The mechanical basis of movement by skeletal muscle

Thin filament proteins skeletal muscle

Troponin, in skeletal muscle

Utilization of Skeletal Muscle Glycogen

© 2024 chempedia.info