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BCH 443 Muscle Tissues Dr. Samina Hyder Haq Dept of Biochemistry King Saud university Functions of Muscle tissues Body movement (Locomotion) Maintenance of posture Respiration Communication (Verbal and Facial) Constriction of organs and vessels Diaphragm and intercostal contractions Peristalsis of intestinal tract Vasoconstriction of b.v. and other structures (pupils) Heart beat Production of body heat (Thermogenesis) Types of Muscle Tissue Skeletal Smooth Attached to bones Makes up 40% of body weight Responsible for locomotion, facial expressions, posture, respiratory movements, other types of body movement Voluntary in action; controlled by somatic motor neurons In the walls of hollow organs, blood vessels, eye, glands, uterus, skin Some functions: propel urine, mix food in digestive tract, dilating/constricting pupils, regulating blood flow, In some locations, autorhythmic Controlled involuntarily by endocrine and autonomic nervous systems Cardiac Heart: major source of movement of blood Autorhythmic Controlled involuntarily by endocrine and autonomic nervous system. Connective Tissue of a Muscle Epimysium. Dense regular c.t. surrounding entire muscle Perimysium. Collagen and elastic fibers surrounding a group of muscle fibers called a fascicle Contains b.v and nerves Endomysium. Loose connective tissue that surrounds individual muscle fibers Separates muscle from surrounding tissues and organs Connected to the deep fascia Also contains b.v., nerves, and satellite cells (embryonic stem cells function in repair of muscle tissue Collagen fibers of all 3 layers come together at each end of muscle to form a tendon or aponeurosis Skeletal Muscle Structure Composed of muscle cells (fibers), connective tissue, blood vessels, nerves Fibers are long, cylindrical, and multinucleated Tend to be smaller diameter in small muscles and larger in large muscles. 1 mm- 4 cm in length Develop from myoblasts; numbers remain constant Striated appearance Nuclei are peripherally located Muscle Fiber Anatomy Sarcolemma - cell membrane Surrounds the sarcoplasm (cytoplasm of fiber) Contains many of the same organelles seen in other cells An abundance of the oxygen-binding protein myoglobin Punctuated by openings called the transverse tubules (T-tubules) Narrow tubes that extend into the sarcoplasm at right angles to the surface Filled with extracellular fluid Myofibrils -cylindrical structures within muscle fiber Are bundles of protein filaments (=myofilaments) Two types of myofilaments 1. Actin filaments (thin filaments) 2. Myosin filaments (thick filaments) – At each end of the fiber, myofibrils are anchored to the inner surface of the sarcolemma – When myofibril shortens, muscle shortens (contracts) Sarcoplasmic Reticulum (SR SR is an elaborate, smooth endoplasmic reticulum runs longitudinally and surrounds each myofibril Form chambers called terminal cisternae on either side of the T-tubules A single T-tubule and the 2 terminal cisternae form a triad SR stores Ca++ when muscle not contracting When stimulated, calcium released into sarcoplasm SR membrane has Ca++ pumps that function to pump Ca++ out of the sarcoplasm back into the SR after contraction SARCOLEMMA Parts of Muscle Sarcomeres: Z Disk to Z Disk Sarcomere - repeating functional units of a myofibril About 10,000 sarcomeres per myofibril, end to end Each is about 2 µm long Differences in size, density, and distribution of thick and thin filaments gives the muscle fiber a banded or striated appearance. A bands: a dark band; full length of thick (myosin) filament M line - protein to which myosins attach H zone - thick but NO thin filaments I bands: a light band; from Z disks to ends of thick filaments Thin but NO thick filaments Extends from A band of one sarcomere to A band of the next sarcomere Z disk: filamentous network of protein. Serves as attachment for actin myofilaments Titin filaments: elastic chains of amino acids; keep thick and thin filaments in proper alignment Structure of Actin and Myosin Myosin (Thick) Myofilament Many elongated myosin molecules shaped like golf clubs. Single filament contains roughly 300 myosin molecules Molecule consists of two heavy myosin molecules wound together to form a rod portion lying parallel to the myosin myofilament and two heads that extend laterally. Myosin heads 1. Can bind to active sites on the actin molecules to form crossbridges. (Actin binding site) 2. Attached to the rod portion by a hinge region that can bend and straighten during contraction. 3. Have ATPase activity: activity that breaks down adenosine triphosphate (ATP), releasing energy. Part of the energy is used to bend the hinge region of the myosin molecule during contraction Thin Filament: composed of 3 major proteins 1. F (fibrous) actin 2. Tropomyosin 3. Troponin Two strands of fibrous (F) actin form a double helix extending the length of the myofilament; attached at either end at sarcomere. Composed of G actin monomers each of which has a myosinbinding site (see yellow dot) Actin site can bind myosin during muscle contraction. Tropomyosin: an elongated protein winds along the groove of the F actin double helix. Troponin is composed of three subunits: Tn-A : binds to actin Tn-T :binds to tropomyosin, Tn-C :binds to calcium ions. Actin (Thin) Myofilament Sliding Filament Model of Contraction Each myosin head binds and detaches several times during contraction, acting like a ratchet to generate tension and propel the thin filaments to the center of the sarcomere As this event occurs throughout the sarcomeres, the muscle shortens Three states of Muscles –Relaxed (low calcium, all Ca+ ions stored in SR –Contracting (Release of high calcium from SR + ATP) –Rigor (high calcium present in sarcoplasm, no ATP The role of Ca+ ions When a muscle is at rest , Ca+ ions are not present in the sarcoplasm because they are stored in sarcoplasmic reticulum. In the absence of Ca + ions in the sarcoplasm, tropomycin prevents the myosin head from attaching onto actin by blocking the binding sites. When a muscle is stimulared sufficiently by nerve impulse, calcium ions are released from the sarcoplasmic reticulum and combine with troponin, causing the tropomycin to change shape and unblock the binding sites. Ca+ ions are released from the sarcoplasmic reticulum at the end of a sequence of events which begins when an action potential reaches the neuromuscular junction. Neuromuscular Junction Muscle Contraction When the action potential arrives, Ca+ ion channels are opened in the membrane of the nerve fibre and ca ion diffuses into the synaptic cleft. This causes synaptic vesicles to move into the junction membrane and fuses with it, releasing acetylcholine into the synaptic cleft. This acetylcholine diffuses across the cleft and attaches onto receptor molecules on the muscle fibre membrane. This leads to graded potential. This action potential sweeps across the muscle fibre and passes to T tubules which causes the sarcoplasmic reticulum to release Ca ions into the sarcoplasm. Ca ions spread through the sarcoplasm. Enabling myosin head to bind onto actin. Energy from ATP enables the head to take new position. Ca ions are pumbed back again into the sarcoplasmic reticulum .tropomycin blocks the myosin head binding site on the actin and the muscle relax. Neuromuscular Junction Region where the motor neuron stimulates the muscle fiber The neuromuscular junction is formed by : 1. End of motor neuron axon (axon terminal) Terminals have small membranous sacs (synaptic vesicles) that contain the neurotransmitter acetylcholine (ACh) 2. The motor end plate of a muscle • A specific part of the sarcolemma that contains ACh receptors Though exceedingly close, axonal ends and muscle fibers are always separated by a space called the synaptic cleft Neuromuscular Junction Figure 9.7 (a-c) The Nerve-Muscle Functional Unit A motor unit is a motor neuron and all the muscle fibers it supplies The number of muscle fibers per motor unit can vary from a few (4-6) to hundreds (12001500) Muscles that control fine movements (fingers, eyes) have small motor units Large weight-bearing muscles (thighs, hips) have large motor units Motor Unit What is rigor mortis Rigor mortis is the stiffening of muscles after death. In both living and dead muscle calcium leaks through the walls of the muscle fibers, and once inside, causes the muscle to contract.. Dead muscle can pump calcium out until it runs out of energy. Once the dead muscle runs out of energy reserves, it cannot pump calcium back out. Therefore it stays contracted. This is called rigor mortis. Over time the dead muscle contracts more and more until it becomes quite tight. Types of muscles Staining of muscle section with special dyes shows these main type of muscle fibre. Type 1 slowly contracting red fibre where aerobic metabolism dominates. Type 11A fiber of intermediate contractibility where both aerobic and anaerobic processes. Type 11B rapidly contracting white fibres where anaerobic metabolism is the major energy supply Energy used in exercise Aerobic(blue) anaerobic(Yellow) Slow twitch fibres Slow twitch fibres are adapted to function over long periods. They respire aerobically to avoid build up of lactic acid. They use muscle glycogen , as they are aerobic they can also use the limitless supply of fat stores in the body.their high content of myoglobib and good blood supply means they obtain sufficient oxygen. Large amounts of mitochondria generate large amount of ATP. Fast-Twitch fibres They are adapted for short burst of explosive action. They generate ATP quickly and anaerobically from stores of high energy compound creatine phosphate and by lactate fermentation. Sources of energy Metabolism ATP IS the "currency" of energy metabolism. Muscle contraction, that is coupling between actin and myosin is powered by ATP (and ONLY ATP). There is only a small amount of this material in muscle cells but this is backed up by several buffer systems. The most rapid of these is the creatine phosphate/creatine phosphokinase system. This is also the smallest reserve and at maximum utilization it is exhausted in about 4 seconds. This is a major source of high-energy phosphate for sprinters.. Sources of Energy The next largest energy source is anaerobic glycolysis. Only glycogen stored in muscles and blood glucose can serve as substrates for anaerobic glycolysis. In quantity, aerobic glycolysis follows, being able to supply enough energy for muscle activity over several hours (dependent upon intensity). Fatty acid oxidation has the largest ATP-producing capacity. This is relatively slow but can produce energy over many hours if work intensity corresponds to the rate of ATP production. It is fascinating to note that the most rapid sources of energy are also the most limited Energy source during exercise Cori cycle diagram Cori cycle or the lactic acid cycle Links for animation http://entochem.tamu.edu/MuscleStrucContra ctswf/index.html http://www.blackwellpublishing.com/matthew s/myosin.html http://msjensen.cehd.umn.edu/1135/Links/Ani mations/Flash/0011-swf_breakdown_of_a.swf