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Chapter 9 Muscular System Skeletal Muscle Each skeletal muscle is an organ made up of skeletal muscle fibers, connective tissue coverings, blood vessels, and nerve fibers Structure of a Skeletal Muscle Outside In • Each skeletal muscle is then covered by an outer, very tough fibrous layer of CT called deep fascia – The deep fascia may extend past the length of the muscle (tendon or aponeurosis), and attach that muscle to a bone, cartilage or muscle • Each skeletal muscle is covered by a second layer of dense, fibrous CT called epimysium A skeletal muscle is composed of a variety of tissues Slide number: 2 Muscle Bone Tendon Fascia (covering muscle) Epimysium Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Skeletal Muscle cont. • Skeletal muscles are formed from bundles of fascicles – Each fascicle is wrapped in a third layer of CT made of collagen called perimysium • Fascicles are formed from bundles of muscle fibers – Each muscle fiber (cell) is wrapped in a thin, delicate (fourth) layer of CT called endomysium – Cell membrane= Sarcolemma – Cytoplasm= Sarcoplasm A skeletal muscle is composed of a variety of tissues Slide number: 5 Muscle Bone Fascicles Tendon Muscle fibers (cells) Fascia (covering muscle) Epimysium Perimysium Endomysium Fascicle Axon of motor neuron Blood vessel Nucleus Sarcoplasmic reticulum Muscle fiber Sarcolemma Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Fascicle Skeletal Muscle cont. • Each muscle fiber contains many threadlike structures called Myofibrils. – Myofibrils play an important role in muscle contraction • They consist of two types of Protein Filaments – Thick filament= Myosin – Thin filament= Actin A skeletal muscle is composed of a variety of tissues Slide number: 7 Muscle Bone Fascicles Tendon Muscle fibers (cells) Fascia (covering muscle) Myofibrils Epimysium Perimysium Thick and thin filaments Endomysium Fascicle Axon of motor neuron Blood vessel Myofibril Nucleus Sarcoplasmic reticulum Muscle fiber Sarcolemma Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Filaments Myofibril Skeletal Muscle Fibers • Within the sarcoplasm (cytoplasm) of a muscle fiber, there are two specialized membranous organelles (“little organs”) • Sarcoplasmic reticulum (SR) – Network of membranous channels that surrounds each myofibril and runs parallel to it – Similar endoplasmic reticulum in other cells – SR has high concentrations of calcium ions compared to the sarcoplasm (maintained by active transport calcium pump) – When stimulated by muscle impulse, membranes become more permeable to calcium ions and calcium diffuses out of SR and into sarcoplasm Skeletal Muscle Fibers cont. • Transverse tubules (TT) – set of membranous channels that extends into the sarcoplasm as invaginations continuous with muscle cell membrane (sarcolemma) – TTs are filled with extracellular fluid and extend deep into the cell – Each TT runs between two enlarged portions of SR called cisternae – These structures form a triad near the region where actin and myosin overlap Skeletal Muscle Fibers cont. • SR and TT are involved in activating the muscle contraction mechanism (discussed in greater detail later). • Because one TT is associated with two SR they are termed the Triad Skeletal Muscle Fibers cont. • The organization of think and thick filaments within muscle fibers produces light and dark bands (striations) characteristic of skeletal muscle fibers • The striations form a repeating pattern of units called sarcomeres. – Functional unit of muscle • Myofibrils are made from sarcomeres in a row, end-to-end. Sarcomere characteristics • I bands=light area = thin filaments alone • A bands=dark area = overlapping of thick and thin filaments • Z lines=Sarcomeres meet one another Sarcomere characteristics cont. • H zone=Lighter area in A bands with only thick filaments • M line=darker area with proteins to hold thick filaments in place Molecules Involved in Contraction Filaments • Thick filaments = protein myosin • Thin filaments = protein actin Other • Tropomyosin • Troponin Molecules Cont. • Thick filaments = protein myosin – rod-like tail (axis) that terminates in two globular heads or cross bridges – Cross bridges interact with active sites on thin filaments • Thin filaments = Primarily the protein actin – coiled helical structure (resembles twisted strands of pearls): – Tropomyosin = rod-shaped protein spiraling around actin backbone to stabilize it Molecules Cont. – Troponin = complex of polypeptides: – one binds to actin – one that binds to tropomyosin – one that binds to calcium ions • Both tropomyosin and troponin help control actin's interaction with myosin during contraction Skeletal Muscle Contraction Neuromuscular Junction • Neuromuscular Junction (NMJ) = the site where a motor nerve fiber and a skeletal muscle fiber meet (also called a synapse or synaptic cleft) – In order for a skeletal muscle to contract, its fibers must first be stimulated by a motor neuron Neuromuscular Junction cont. • Motor End Plate = the specific part of a skeletal muscle fiber's sarcolemma directly beneath the NMJ • Neurotransmitter = chemical substance released from a motor end fiber, causing stimulation of the sarcolemma of muscle fiber; acetylcholine (ACh) • Synaptic cleft – small space between neuron and muscle Motor Unit • Motor Unit = one motor neuron and many skeletal muscle fibers Stimulus for Contraction Introduction • • • The function of skeletal muscle is to move bones of the skeleton under voluntary control. Contraction of a skeletal muscle fiber is a complex interaction of several cellular and chemical constituents. The final result is a movement whereby actin and myosin filaments slide past one another. – The muscle fiber shortens and pulls on its attachments. Stimulus for Contraction • The process begins when a nerve impulse is initiated by the brain, travels down the spinal cord, into a motor neuron, which branches into many motor nerve fibers/endings • The neuron meets the muscle at the neuromuscular junction • Neurotransmitter (Acetylcholine) is released into the NMJ (via exocytosis) Stimulus for Contraction cont. • Acetylcholine diffuses across the NMJ and creates an electrical signal (similar to a nerve impulse) at the motor end-plate (sarcolemma) – The electrical signal is created by the movement of ions – It must reach a certain strength for contraction to be stimulated • The muscle impulse travels over the surface of the skeletal muscle fiber and deep into the muscle fiber by means of the Transverse Tubules – This instigates the process of muscle contraction Excitation Contraction Coupling Big Picture • The muscle impulse reaches the sarcoplasmic reticulum, which releases calcium ions into the cytosol • Calcium binds to troponin, moving tropomyosin and exposing myosin binding sites on actin filament • Cross-bridges (linkages) form between actin and myosin • Actin filaments are pulled inward by myosin crossbridges • The muscle fiber shortens as contraction occurs Sliding Filament Theory • states that muscle contraction involves the sliding movement of the thin filaments (actin) past the thick filaments (myosin) – Resulting in shortening of sarcomeres • A relaxed muscle cell, overlapping of thick and thin filaments is only slight • Changes in muscle during contraction: – The distance between the Z-lines of the sarcomeres decreases – The I-Bands (light bands) shorten • The A-Bands move closer together, but do not diminish in length. When a skeletal muscle contracts Slide number: 3 Sacromere A band Z line Z line Actin filaments 1 Relaxed Myosin filaments Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. When a skeletal muscle contracts Slide number: 4 Sacromere A band Z line Z line Actin filaments 1 Relaxed Myosin filaments 2 Contracting Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. When a skeletal muscle contracts Slide number: 5 Sacromere A band Z line Z line Actin filaments 1 Relaxed Myosin filaments 2 Contracting 3 Fully contracted Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Cross-bridge Cycling • when calcium ions are present, the myosin binding sites on actin are exposed • myosin cross-bridge attaches to actin binding site • myosin cross-bridge pulls thin filament • ADP and phosphate released from myosin • new ATP binds to myosin Cross-Bridge Cycling cont. • linkage between actin and myosin crossbridge break • ATP splits • myosin cross-bridge goes back to original position * As long as calcium ions and ATP are present, this walking continues until the muscle fiber is fully contracted Slide number: 1 Tropomyosin Troponin complex Actin monomers ADP + P ADP + P Myosin filament Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Actin filament Slide number: 2 Tropomyosin Troponin complex Actin monomers ADP + P ADP + P Myosin filament Ca+2 Muscle contraction Release of Ca+2 from sarcoplasmic reticulum exposes binding sites on thin filament: Ca+2 binds to troponin complex Tropomyosin pulled aside Binding sites on actin filament exposed Ca+2 ADP + P Ca+2 ADP + P Ca+2 1 Exposed binding sites on actin allow the muscle contraction cycle to occur Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Actin filament Slide number: 3 Contraction cycle Ca+2 ADP + P Ca+2 ADP + P Ca+2 ADP + P ADP + P 2 Cross-bridge binds actin to myosin Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Slide number: 4 Contraction cycle ADP + P ADP P ADP P ADP + P 3 Cross-bridge pulls actin filament (power stroke), ADP and P released from myosin Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ADP + P Slide number: 5 Contraction cycle ATP ATP ATP 4 New ATP binds to myosin, causing linkage to release ATP ADP P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ADP P Slide number: 6 Contraction cycle ADP + P ADP + P 5 ATP splits, which provides power to “cock” the myosin cross-bridge ATP ATP ATP Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Slide number: 7 Contraction cycle Ca+2 ADP + P ADP + P Ca+2 ADP + P Ca+2 ADP + P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Slide number: 8 ADP + P ADP + P Ca+2 Muscle relaxation Active transport of Ca+2 into sarcoplasmic reticulum, which requires ATP, makes myosin binding sites unavailable. ATP Ca+2 ADP + P Ca+2 ADP + P Ca+2 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Slide number: 9 Ca+2 ADP + P Ca+2 ADP + P Ca+2 1 Exposed binding sites on actin allow the muscle contraction cycle to occur ADP + P Contraction cycle ADP + P 5 ATP splits, which provides power to “cock” the myosin cross-bridge ATP ADP + P ADP + P 2 Cross-bridge binds actin to myosin ATP ADP ATP P ATP 4 New ATP binds to myosin, causing linkage to release ADP P ADP + P 3 Cross-bridge pulls actin filament (power stroke), ADP and P released from myosin Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Slide number: 10 Tropomyosin Troponin complex Actin monomers ADP + P ADP + P Myosin filament Ca+2 Ca+2 Muscle contraction Muscle relaxation Release of Ca+2 from sarcoplasmic reticulum exposes binding sites on thin filament: Ca+2 binds to troponin complex Active transport of Ca+2 into sarcoplasmic reticulum, which requires ATP, makes myosin binding sites unavailable. ATP Tropomyosin pulled aside Binding sites on actin filament exposed Ca+2 ADP + P Ca+2 ADP + P Ca+2 1 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Actin filament Relaxation • • Acetylcholinesterase is an enzyme present in the NMJ It immediately destroys acetylcholine, so the motor end-plate is no longer stimulated – i.e. it cannot cause continuous muscle contraction • • • Calcium ions are transported from sarcoplasm back into sarcoplasmic reticulum Linkages between actin and myosin are broken The muscle fiber relaxes Energy Sources for Contraction The energy used to power the interaction between actin and myosin comes from ATP Introduction • ATP stored in skeletal muscle lasts only about six seconds • ATP must be regenerated continuously if contraction is to continue • There are three pathways in which ATP is regenerated: – Coupled Reaction with Creatine Phosphate – Anaerobic Cellular Respiration (Ch. 4) – Aerobic Cellular Respiration (Ch. 4) Coupled Reaction with Creatine Phosphate (CP) • CP + ADP <------> creatine + ATP • Muscle stores a lot of CP • This coupling reaction allows for about 10 seconds worth of ATP Oxygen Supply and Cellular Respiration • Anaerobic Respiration – Steps are called glycolysis – Steps occur in the cytoplasm of the cell – Results in production of pyruvic acid and 2 ATP • Aerobic Respiration (bet you thought you were done with this!) – Steps are called citric acid cycle and electron transport chain – Oxygen is required – Steps occur in the mitochondrion of the cell – Results in CO2, water and 36ATP Muscle Fatigue • • • Muscle fatigue is a state of physiological inability to contract If no oxygen is available in muscle cells to complete aerobic respiration, pyruvic acid is converted to lactic acid, which causes muscle fatigue and soreness Results from a relative deficit of ATP and/or accumulation of lactic acid (which decreases pH) Oxygen Debt • The oxygen debt is the amount of oxygen necessary to support the conversion of lactic acid to glycogen • needed to replenish spent glycogen stores • oxygen not available – glycolysis continues – pyruvic acid converted to lactic acid – liver converts lactic acid to glucose Heat Production • Almost half of the energy released during muscle contraction is lost to heat, which helps maintain our body temperature at 37o C • Excessive heat is lost through many negative feedback mechanisms (discussed in chapter 1) including sweating, dilation of superficial blood vessels, increased breathing rate, and increased heart rate Muscle Responses Threshold Stimulus • • The minimal strength of stimulation required to cause contraction A skeletal muscle fiber’s resting membrane potential must be depolarized from –100mV to –70mv before an impulse begins • Therefore the threshold stimulus is +30mV Recording a Muscle Contraction • • • • A myogram is a recording of a muscle contraction A twitch is a single contraction that lasts a fraction of a second, followed by relaxation The delay between stimulation and contraction is called the latent period A muscle fiber must return to its resting state (-100mV) before it can be stimulated again – This is called the refractory period All-or-Nothing Response • If a muscle fiber is brought to threshold or above, it responds with a complete twitch • If the stimulus is sub-threshold, the muscle fiber will not respond Summation • When several stimuli are delivered in succession to a muscle fiber, it cannot completely relax between contractions – • The individual twitches begin to combine and the muscle contraction becomes sustained In a sustained contraction, the force of individual twitches combines in a process called summation – can lead to tetanic contractions Tetanus • When the resulting sustained contraction lacks even slight relaxation, it is called titanic contraction • Incomplete tetanus=the state of a muscle at maximum tension that is not allowed to relax completely • Complete tetanus=the muscle is at maximum tension and there is no relaxation phase at all Motor Units • • • Definition: A motor unit is a motor neuron and the many skeletal muscle fibers it stimulates Because the motor neuron branches into several motor nerve endings, it can stimulate many skeletal muscles fibers simultaneously, which then contract simultaneously The number of muscle fibers in a motor unit varies from 10-hundreds Recruitment • • • • A muscle is composed of many motor units, controlled by many different motor neurons recruitment - increase in the number of motor units activated more precise movements are produced with fewer muscle fibers within a motor unit as intensity of stimulation increases, recruitment of motor units continues until all motor units are activated Muscle Tone • Sustained Contractions – Even when a muscle is at rest, a certain amount of sustained contraction is occurring in its fibers. This is called muscle tone. • Muscle tone is very important in maintaining posture Types of Contractions • isotonic – muscle contracts and changes length • concentric – shortening contraction • eccentric – lengthening contraction • isometric – muscle contracts but does not change length Fast and Slow Muscle Fibers • Muscle fibers vary in contraction speed (i.e. slow or fast twitch) • Slow-Twitch Fibers are also called red fibers – contain oxygen carrying pigment, myoglobin, receive a rich blood supply, and contain many mitochondria – can generate ATP fast enough to keep up with breakdown – These fibers contract for long periods without fatiguing • Fast-twitch fibers are also called white fibers – contain less myoglobin, blood, and fewer mitochondria. – contain extensive sarcoplasmic reticulum to store and reabsorb calcium – These fibers contract rapidly, but fatigue easily due to lactic acid accumulation Smooth Muscle The contraction mechanism of smooth muscle is similar to that of skeletal muscle in that interaction occurs between actin and myosin, however the transverse tubules and sarcoplasmic reticula are greatly reduced, and troponin is absent. Smooth Muscle Fibers Multi-unit smooth muscle • location – irises of eyes – walls of blood vessels • Contraction is rapid and vigorous (similar to skeletal muscle tissue) • less organized • function as separate units – fibers function separately Smooth Muscle Fibers cont. Visceral smooth muscle • Location = the walls of hollow organs • Contraction is slow and sustained – Rhythmicity = pattern of repeated contractions – Peristalsis = wave-like motion that helps push substances through passageways • Structure: – – – – – single-unit smooth muscle sheets of muscle fibers fibers held together by gap junctions random arrangement of actin and myosin filaments Two layers of muscle surround the passageway • inner circular layer • outer longitudinal layer Smooth Muscle Contraction • A protein, calmodulin binds to calcium ions (no troponin) and activates the contraction mechanism • Most calcium diffuses in to smooth muscle cells from the extracellular fluid (reduced SR). • Norepinephrine and acetylcholine are smooth muscle neurotransmitters • Smooth muscle slower to contract and relax • Smooth muscle more resistant to fatigue • Stretching can trigger smooth muscle contraction • Smooth muscle can change length without changing tautness CARDIAC MUSCLE Will be studied in greater detail in Chapter 15 Cardiac Muscle • Location=the heart • Anatomy: – Striated uninuclear cells joined end-to-end forming a network – Cell junctions are called intercalated discs • Arrangement of actin and myosin not as organized as skeletal muscle • Contains sarcoplasmic reticula, transverse tubules, and numerous mitochondria • Sarcoplasmic reticulum is less developed than SR in skeletal muscle and stores much less calcium Cardiac Muscle cont. Physiology • Self-exciting tissue (i.e. “Pacemaker”) • Rhythmic contractions (60-100 beats/minute) • Involuntary, all-or-nothing contractions • Pumps blood to: – Lungs for oxygenation – Body for distribution of oxygen and nutrients SKELETAL MUSCLE ACTIONS Skeletal muscles generate a great variety of body movements. The action of a muscle primarily depends upon the joint associated with it and the manner in which the muscle is attached on either side of that joint Origin and Insertion • Recall that skeletal muscles are usually attached to a fixed body part and a movable body part: – The origin of a muscle is its immovable (anchored) end – The insertion of a muscle is the movable end of a muscle • When a muscle contracts and shortens, its insertion is pulled toward its origin Skeletal Muscle Actions • Flexion = decreasing the angle between 2 bones – Dorsiflexion = decreasing the angle between the foot and shin – Plantar flexion = pointing toes • Extension = increasing the angle between 2 bones • Abduction = moving a body part away from the midline • Adduction = moving a body part toward the midline • Circumduction = movement in a circular (cone-shaped) motion • Rotation = turning movement of a bone about its long axis – (i.e. atlas/axis) • • • • • Supination = thumbs up Pronation = thumbs down Inversion = sole of foot in Eversion = sole of foot out Elevation = lifting a body part – (i.e. shoulder shrug) • Depression = returning a body part to pre-elevated position Interactions of Skeletal Muscles • Prime Mover (agonist) = the primary muscle responsible for a movement – The biceps brachii in flexing the arm at the elbow • Antagonist(s) = the muscle(s) in opposition to the action of the prime mover. The antagonist relaxes (or stretches) during the prime movement – The triceps brachii is the antagonist of the biceps brachii when we flex the arm at the elbow • Synergist(s) = muscles that assist the prime mover – The brachialis helps the biceps brachii during elbow flexion • Fixators = muscle groups that stabilize the origin of the prime mover (i.e. hold it in place) so that the prime mover can act more efficiently – The scapula is the origin for many arm muscles, but it must be held in place by fixator muscles in order to function in this way • serratus anterior • pectoralis minor LIFE SPAN CHANGES • Supplies of ATP, myoglobin, and creatine phosphate in muscle fibers begin to decline in one’s forties • Half of one’s muscle mass has been replaced by connective and adipose tissue by age 80, and reflexes are reduced • Exercise is the best way to maintain muscle function