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140 Cards in this Set
- Front
- Back
epimysium
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the connective tissue covering the whole muscle
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perimysium
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the connective tissue covering of the muscle bundle/fascicle
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endomysium
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the connective tissue covering of the muscle fiber
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actin
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this protein is located in the thin filament; binds to myosin to produce a cross bridge
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alpha-actinin
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this protein anchors actin to the Z disc in the sarcomere
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Laminin
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this protein is located in the lamina lucida layer of the basal lamina; it contributes to cell attachment (exists with the costamere)
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myosin
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protein located in the center of the sarcomere, and is the major component of the thick filament; it binds to actin to produce a cross bridge
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tropomyosin
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protein located in a groove along the length of the actin filament; it covers the myosin binding sites on actin to prevent cross bridges from being formed
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troponin
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protein that is bound to both actin and tropomyosin; when calcium binds to it, tropomyosin changes and the actin binding sites are exposed so cross bridges can be formed
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nebulin
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protein that is connected to actin; appears to contribute to assembly and regulation of thin filament length
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titin
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this protein connects myosin filaments from the M line to the nearest Z disc; it maintains myofibrillar lattice structure and contributes to the passive tension of the muscle
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Z discs
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these are the dark lines that bisect the I bands of thin filament; demarcate the sarcomere
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M line
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the dense zone in the center of the A band of thick filaments
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myosin binding proteins
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proteins that provide a framework/scaffold to stabilize thick filament and guide the filament development during myogenesis
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desmin
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this is a protein that is the major part of intermediate filament system; it connects the outer Z disc to the sarcolemma and also tethers the Z disc to the mitochondria and myonuclei; it plays a critical role in maintaining registry between adjacent Z discs
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dystrophin
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protein located in the subsarcolemmal region; it stabilizes the membrane ion channels during contraction and relaxation; it links the dystrophin associated proteins to actin
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dystrophin associated proteins
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this protein complex spans the sarcolemma and is thought to play a critical role in linking the actin cytoskeleton to the extracellular matrix
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costamere
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these structures are located below the sarcolemma; they couple force-generating sarcomeres with the sarcolemma and anchor the sarcolemma with the Z discs, M lines, and at the musculoskeletal junction
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creatine kinase
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this is an enzyme located within the thick filament that helps to regulate ATP levels in the muscle cell
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basal lamina
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this membrane forms a network that links skeletal muscle proteins to the sarcolemma, providing lateral transmission of force; it maintains muscle integrity as well. It is required for muscle repair and is a selective permeability layer
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DHP receptors
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these receptors are located in the T tubule; they sense the change in voltage during an action potential
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RyR
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these receptors are located on the sarcoplasmic reticulum and are a calcium release channel
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calsequestrin
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this protein is located in the sarcoplasmic reticulum; it binds and stores calcium
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SERCA
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this is a calcium ATPase transporter that pumps calcium back into the SR
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phospholamban
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this is a protein that regulates the activity of SERCA (when phosphorylated, increases SERCA activity)
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myoD myfd5
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these myogenic regulatory factors are involved in determination (create myoblasts)
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mrf4 and myogenin
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these myogenic regulatory factors are expressed later and are involved in differentiation (cause myoblasts to proliferate and fuse into myotubes for muscle development to proceed)
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plasma membrane
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this cell organelle separates the interior of the cell from the outside; it is an attachment point for the intracellular cytoskeleton; it attaches the ECM to other cells to help group the cells together to form tissues
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mitochondria
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this cell organelle generates most of the ATP used to supply the cell; it regulates cell metabolism and can regulate homeostasis of calcium and membrane potential
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myonuclei
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these organelles are responsible for a "domain"; they secrete different growth factors that support growth and repair of the cell
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sarcoplasmic reticulum
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this organelle is directly involved in the storage of calcium and the removal of calcium from myofilaments to relax muscle; it is the middleman between skeletal muscle activation and relaxation
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twitch
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the response of one single muscle fiber to a single action potential
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unfused tetany
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when a set of repeating action potentials activates the muscle fiber before the relaxation of the previous twitch; can still distinguish between contractile events
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fused tetay
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the time interval between activation of successive twitches has shortened and the twitches fuse into a single, stable level of muscle
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motor unit
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the alpha motor neuron and all the fibers it innervates
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calcineurin/NFAT
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the main pathway for myofiber transition
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Akt, mTOR
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the main pathways for muscle hypertrophy
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myostatin, FOXO, urfs, atrogin, ubiquitin ligase
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the main pathways for muscle atrophy
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Akt
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these proteins inhibit cell apoptosis and can also induce protein synthesis pathways, so it is therefore a key signaling protein in the cellular pathways that lead to skeletal muscle hypertrophy
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atrogin
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this protein mediates proteolysis events that occur during muscle atrophy; it is thought to recognize and bind to some proteins to promote their degradation during atrophy
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mTOR
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this protein integrates the input from pathways, senses cellular nutrient and energy levels and determines if there is enough to cause hypertrophy
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myopathy
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a muscular disease in which the muscle fibers do not function for reasons, resulting in muscular weakness
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sarcopenia
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the degenerative loss of skeletal muscle mass and strength that is associated with aging
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NCAM
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this molecule is expressed on the primitive myotubes following denervation to perhaps "guide" incoming nerves to the muscle fiber; thought to signal to induce neurite outgrowth
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CALPAIN
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enzymes that are activated when calcium levels rise too high; cause regeneration
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calcineurin/NFAT
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this pathway is the activity-dependent transformation of fast fibers into slow fibers
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epithelial
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these types of cells form a continuous layer that line the surfaces of organs; form a selective permeability layer, secrete substances, and protect from danage
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unilaminar
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epithelial cells that form a single layer in adjacent tissues (squamous, cuboidal)
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multilaminar
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epithelial cells that form multiple layers (stratified squamous, stratified cuboidal or columnar)
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exocrine
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glands that secrete onto external surfaces through ducts
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endocrine
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glands that are ductless and secrete messengers into the blood (insulin)
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paracrine
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glands that secrete substances into the extracellular fluid compartment
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special skeletal
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this type of connective tissue consists of cartilage and bone and includes chondrocytes, osteocytes, osteoblasts, and osteoclasts; they are found embedded in a matrix that they secrete
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general type
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the type of connective tissues that are subdivided into resident and transient immigration cells
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resident
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cells of the general type of connective tissues that stay fixed in location and include fibroblasts, adipocytes, macrophages, pericytes, and mast cells
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transient
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these types of general type of connective tissues originate in the bone marrow and circulate int he bloodstream, then leave the circulation and enter the connective tissue to perform their specific function; are B and T lymphocytes, plasma cells, neutrophils, eosinophils, basophils, monocytes, and macrophages
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collagen and elastin
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these are the insoluble protein fibrils of the extracellular matrix
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collagen
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a structural protein that is about 30% of the body's proteins; there are many types and contain hydroxyproline and three polypeptides arranged in helices
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elastin
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these fibers are synthesized by fibroblasts and smooth muscle cells; they stretch easily with near perfect recoil, but calcify with age; surrounded by a sheath of microfibrils and are responsible for the elasticity of connective tissue
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soluble polymers
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ground substance of the ECM; hydrated gel like material that absorbs compressive forces and composed of three families of macromolecules
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glycosaminoglycans (GAG)
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these proteins are negatively charged chains of repeating disaccharide units that possess high osmotic activity and are therefore capable of binding large amounts of water; they resist compression forces
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proteoglycans
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sulfated GAGs that form covalent bonds with a protein core; located in the ground substance of the ECM and they resist compression, retard microorganisms, form molecular filters, possess binding sites for signaling molecules and function as cytoskeletal components
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cell adhesive glycoproteins
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located in the ground substance of the ECM; allow for cells to adhere to the components of the ECM
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fibronectin
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type of glycoprotein that is synthesized by fibroblasts and act as guidance pathways for the embryonic cells and also function in wound repair
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laminin
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a glycoprotein that is found in the basal lamina and binds with type IV collagen and the cell membrane
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tenascin
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a glycoprotein that is limited to embryonic tissue where it functions as a migratory path for cell migrations and axon growth
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basal lamina
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consists of two layers, the lamina lucida and the lamina densa
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lamina lucida
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this layer of the basal lamina consists of the extracellular glycoproteins and transmembrane glycoproteins
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lamina densa
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this layer of the basal lamina is made up of a meshwork of type IV collagen
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lamina reticularis
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this layer is made up of type I, III, and VII collagen, and it serves as an interface between the basal lamina and the connective tissues
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glycocalyx
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this is a cell coat that consists of glycoproteins and glycolipids that form an integral part of the plasma membrane; cell antigens may be found here and also specialized adhesion molecules
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tight junctions
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these types of junctions regulate the passage of molecules between cells
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gap
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these types of junctions allow for communication between adjacent cells
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demosomes
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these types of junctions function to hold adjacent cells firmly together in areas of mechanical stress
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adherence
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these types of junctions link actin fibers between adjacent cells
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cell matrix
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these types of junctions anchor cytoskeletal proteins to ECM macromolecules
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focal adhesions
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these junctions link intracellular actin fibers to ECM proteins
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hemidesmosome
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these junctions link intracellular cytoskeletal proteins to ECM proteins
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homeostasis
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constancy of the internal environment
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2/3
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intracellular fluid represents ___ of total body water
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1/3
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extracelllular fluid represents ___ of total body water and is composed of two volumes of fluid
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interstitial fluid
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one component of extracellular fluid that is 80%
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plasma volume
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one component of extracellular fluid that is 20%
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40-70%
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TBW comprises __ to __ % of total body mass
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fibroblasts
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a type of resident cell that is flattened and irregular with branching processes; it synthesizes most of the ECM of the connective tissue, therefore are highly active; they adhere to collagen and elastin and play a major role in wound repair
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adipocytes
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function in synthesis, storage, and release of fat from glycerol, fatty acids, and glucose; synthesize and secrete a number of chemical messengers and are now considered to be a major endocrine organ
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macrophages
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resident cells that functions as phagocytes (eliminate foreign substances by engulfing them); play many important roles in inflammation (synthesize and secrete cytokines)
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pericytes
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resident cells that surround the endothelial cells of capillaries;they share the basal lamina of endothelial cells and may undergo differentiation to become smooth muscle cells and endothelial cells in the walls
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mast cells
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these cells are derived from bone marrow cells, and function in mediation inflammation; they are the largest of fixed connective tissue cells, and secrete many substances
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excitability, elasticity, contractility, relaxation
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the four differentiated functions of muscle cells
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satellite
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these cells are located out of the plasma membrane but within/below the basal lamina; they are stem cells and are the sole source of postnatal myonuclei
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3-10%
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satellite cells represent between __ and __ of all muscle nuclei
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sarcolemma
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this skeletal muscle membrane includes both the basal lamina and the plasma membrane
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myoplasticity
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the capacity of muscle for adaptive change
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sugar, phosphoric acid, nitrogen base
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the three components of nucleotides
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mRNA
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RNA that encodes the protein
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rRNA
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RNA part of the ribosome that is used to translate mRNA into a protein
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tRNA
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RNA that couples the region which binds the mRNA codon and its amino acid; transports the protein coded on mRNA
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transcription
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the process of making an RNA copy of a single gene
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RNA polymerase
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the enzyme that aids in transcription
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5-3
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the direction in which transcription occurs down the DNA molecule
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exons
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the parts of the mRNA copy that will be expressed
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introns
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the parts of the mRNA copy that will be snipped out and not expressed
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translation
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the process of reading the RNA sequence of an mRNA and creating the amino acid sequence of a protein
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64, 20
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there are __ possible codons that code for __ different amino acids in the body
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AUG, methionine
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the start codon in translation is __, which codes for the protein __
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N terminal
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the location on the first amino acid of a protein that contains a free amino group
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C terminal
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the location on the last amino acid of a protein that has a free acid group
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3'
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the amino acid on the tRNA is attached to the __ end
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aminoacyl tRNA synthetases
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enzymes used to charge the tRNA with the proper amino acid
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release factors
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during translation, these proteins bind to the stop codon, causing the ribosome, the mRNA , and the new polypeptide to separate
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polypeptides
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linear chains of amino acids
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primary structure
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the sequence of amino acids in a polypeptide is known as its __ structure
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peptide
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the bonds that are formed between the acid group of one protein and the amino group of the other protein
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secondary
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this structure is a conformation of a short peptide, mainly determined by hydrogen bonds (alpha helix and beta pleated sheets)
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tertiary
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this protein structure is the conformation of a whole polypeptide chain
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slow twitch (type I)
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these types of fibers have a slow contraction time, are highly resistant to fatigue, smaller, have high mitochondrial and myoglobin density, high levels of oxidative enzymes and low levels of glycolysis
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FOG (Type IIA)
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these types of fibers are moderate in resistance to fatigue and have high mitochondrial density; they are high in creatine phosphate and glycogen, and have high glycolytic and oxidative enzyme activity
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FG (Type IIB)
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these types of fibers are sensitive to fatigue and are short anaerobic fibers; they are large and have low mitochondrial density and myoglobin; high in creatine phosphate and glycogen, so high glycolytic enzyme content and low oxidative content
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fast
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the SR and T-system occupies 2-3 times more volume in __ fibers
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intrafusal
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these types of fibers are part of the muscle spindle and are innervated by gamma motor neurons; they are proprioceptive in nature
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extrafusal
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these types of fibers are innervated by alpha motor neurons and contract, generating skeletal movement
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PEVK
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this region in titin is the spring-like elastic element
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nicotinic
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the receptor on the postsynaptic terminal for ACh is a __ type or receptor
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myopathy
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a variation in fiber type size (degeneration and regeneration of muscle fibers)
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dystrophy
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replacement of muscle fibers with increased connective tissue
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atrophy
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the active process of increase in protein degradation and a decrease in protein synthesis
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endurance
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__ training leads to more type I fibers
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strength
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__ training leads to more type II fibers
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type II
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type __ fibers are selectively atrophied during disuse
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cachexia
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a wasting syndrome that is a loss of weight, muscle atrophy, fatigue, weakness, and significant loss of appetite in someone who is not trying to lose weight; basically a loss of body mass that cannot be reversed nutritionally
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tumor necrosis factor a, or cachexin
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thought to be the most likely mediator of cachexia
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sarcopenia
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muscle weakness and wasting in the elderly possibly due to a decrease in the proliferative capacity or number of satellite cells or accumulating mitochondrial DNA deletion
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critical illness myopathy
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muscle weakness that is prevalent in patients receiving intensive care during a critical illness; hallmark is loss of myosin
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7-10
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half life of muscle structural proteins is __-__ days
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days or hours
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the time course of atrophy is __ or __
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days
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the time course of hypertrophy is __
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FOXO
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these proteins induce the ubiquitin ligase pathway and cause muscle atrophy
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ubiquitin ligase
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the pathway for muscle atrophy that is caused by an attachment of ubiquitin and lysine, targeting specific protein substrates for degradation
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myostatin
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a signaling molecule that is secreted by muscle and negatively regulates muscle mass; it is thought to regulate the proliferation of muscle stem cells and decreases satellite cell incorporation and myoblast differentiation; it also inhibits Akt protein synthesis
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