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Muscle Activation, Growth and Disease

Muscle Activation, Growth and Disease. motor unit : minimum unit of contraction. Spinal cord. Motor unit 1. Motor unit 2. Synaptic terminals. Fig. 50-30. Nerve.

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Muscle Activation, Growth and Disease

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  1. Muscle Activation, Growth and Disease

  2. motor unit: minimum unit of contraction Spinal cord Motorunit 1 Motorunit 2 Synaptic terminals Fig. 50-30 Nerve • All motor neurons leading to skeletal muscles have branching axons, each of which terminates in a neuromuscular junction with a single muscle fiber. Motor neuroncell body Motor neuronaxon • Nerve impulses passing down a single motor neuron will thus trigger contraction in all the muscle fibers at which the branches of that neuron terminate. Muscle Muscle fibers Tendon

  3. Put it all together… 1 2 3 ATP 7 4 6 ATP 5

  4. Botox • Bacteria Clostridiumbotulinum toxin • blocks release of acetylcholine • botulism can be fatal muscle

  5. Motor Units Size of the motor unit = amount of control a single motor neuron triggers fewer than 10 fibers in the muscles controlling eye movements the motor units of the muscles controlling the larynx are as small as 2–3 fibers per motor neuron In contrast, a single motor unit for a muscle like the gastrocnemius (calf) muscle may include 1000–2000 fibers (scattered uniformly through the muscle).

  6. NS has 2 mechanisms for controlling graded whole muscle contractions • Recruitment: strength is determined by the number of motor units participating and/or by selecting large or small motor units 2. Varying rate of muscle fiber stimulation Don’t forget a nerve impulse is All or None!!!

  7. Do Muscles ever REST? • Tonus: skeletal muscles are in a state of partial contraction , • The state of activity or tension of a muscle beyond that related to its physical properties, that is, its active resistance to stretch. In skeletal muscle, tonus is dependent upon efferent innervation. (Stedman, 25th ed) • is maintained by the activation of a few motor units at all times even in resting muscle. • As one set of motor units relaxes, another set takes over.

  8. Force (tension) developed by a muscle progressively increases as more and more of the motor neurons controlling the muscle are activated Tension

  9. Alternate Activation • Posture muscles are always partially contracted • NS may alternate activation of motor units • Reducing time any one set of fibers is contracted

  10. Gentle pressure Fig. 50-UN2 Sensoryreceptor Low frequency of action potentials More pressure (a) Single sensory receptor activated High frequency of action potentials Gentlepressure Fewer receptorsactivated Sensoryreceptors Morepressure More receptorsactivated (b) Multiple receptors activated

  11. Varying rate of muscle fiber stimulation • 1 action potential (twitch) lasts <100msec • If another ap arrives before fiber is relaxed , the two twitches add together = greater tension • Further summation occurs as the rate of stimulation increases • When the rate is high enough and the muscle fiber cannot relax at all between stimuli the twitches fuse into one smooth sustained contraction called - tetanus

  12. Myogram: graph of twitch contraction Contraction period: Repetitive power strokes Generating force /tension Relaxation period: power strokes are decreasingLevels of Ca2+ decreasing How is this happening? Latent period: Time for Ca2+ to be released from SR to bind to troponin Why do we need this step? stimulus

  13. Tetanus When shocks are given at 1/sec, the muscle responds with a single twitch. At 5/sec and 10/sec, the individual twitches begin to fuse together, a phenomenon called clonus. At 50 shocks per second, the muscle goes into the smooth, sustained contraction of tetanus. Clonus and tetanus are possible because the refractory period is much briefer than the time needed to complete a cycle of contraction and relaxation. Note that the amount of contraction is greater in clonus and tetanus than in a single twitch. As we normally use our muscles, the individual fibers go into tetanus for brief periods rather than simply undergoing single twitches.

  14. Tetanus Fig. 50-31 Summation oftwo twitches Tension Singletwitch Time Actionpotential Series of actionpotentials athigh frequency Pair ofactionpotentials

  15. The contraction of skeletal muscle is controlled by the nervous system. The Dying Lioness (an Assyrian relief dating from about 650 B.C. and supplied through the courtesy of The Trustees of the British Museum) shows this vividly. Injury to the spinal cord has paralyzed the otherwise undamaged hind legs. Activation of Skeletal Muscle • In this respect, skeletal muscle differs from smooth and cardiac muscle. Both cardiac and smooth muscle can contract without being stimulated by the nervous system. Nerves of the autonomic branch of the nervous system lead to both smooth and cardiac muscle, but their effect is one of moderating the rate and/or strength of contraction.

  16. Heartbeat ANS does run to the heart = modulate • increase or decrease • the intrinsic rate • the strength of the heartbeat Even if the nerves are destroyed (as they are in a transplanted heart), the heart continues to beat. Gap junctions STRUCTRE =FUNCTION Significance: All the fibers contract in a synchronous wave that sweeps from the atria down through the ventricles and pumps blood out of the heart.

  17. Anything that interferes with this synchronous wave (such as damage to part of the heart muscle from a heart attack) may cause the fibers of the heart to beat at random — called fibrillation. Fibrillation is the ultimate cause of most deaths and its reversal is the function of defibrillators that are part of the equipment in ambulances, hospital emergency rooms, and — recently — even on U.S. airlines

  18. Does the heart go into tetanus? • The refractory period in heart muscle is longer than the period it takes for the muscle to contract (systole) and relax (diastole). Thus tetanus is not possible (a good thing, too!). • Cardiac muscle has a much richer supply of mitochondria than skeletal muscle. This reflects its greater dependence on cellular respiration for ATP. • STRUCTURE = FUNCTION • Cardiac muscle has little glycogen and gets little benefit from glycolysis when the supply of oxygen is limited. • Thus anything that interrupts the flow of oxygenated blood to the heart leads quickly to damage — even death — of the affected part. This is what happens in heart attacks.

  19. Isotonic versus Isometric Contractions • Isotonic: the muscle is allowed to shorten • Isometric: a stimulated muscle is held so that it cannot shorten, it simply exerts tension.

  20. Muscle OK now we know how to get a muscle to contract and how to get gradients of strength…. Now how do we get stronger? Strength= size of contractile force (cross section of the muscle’s belly) Endurance : increases in CP MB Glycogen Lung capacity RBC count Fig. 50-25a Bundle ofmuscle fibers Nuclei Single muscle fiber(cell) Plasma membrane Myofibril Z lines Sarcomere

  21. How muscles grow initially Skeletal muscle forms by fusion of mononucleated myoblasts to form mutinucleated myotubes. If it tried to divide, it would have several dozen or hundreds of spindles = MESS • Some Recent Findings • Satellite cells - Day K, Shefer G, Richardson JB, Enikolopov G, Yablonka-Reuveni Z. Nestin-GFP reporter expression defines the quiescent state of skeletal muscle satellite cells. Dev Biol. 2006 Dec 15; • "Repair of adult skeletal muscle depends on satellite cells, quiescent myogenic stem cells located beneath the myofiber basal lamina. ...

  22. The number of fibers is probably fixed early in life. This is regulated by myostatin, a cytokine that is synthesized in muscle cells (and circulates as a hormone later in life). • Myostatin suppresses skeletal muscle development.. Inactive Oncogene? Some athletes and other remarkably strong people have been found to carry one mutant myostatin gene Cattle and mice with inactivating mutations in their myostatin genes develop much larger muscles. • Growing illicit market in drugs supposedly able to suppress myostatin.

  23. In adults, increased strength and muscle mass Interesting note: In the mouse, at least, fibers increase in size by attracting more myoblasts to fuse with them. The fibers attract more myoblasts by releasing the cytokine interleukin 4 (IL-4). Anything that lowers the level of myostatin also leads to an increase in fiber size. increase in the thickness of the individual fibers increase in the amount of connective tissue Increase of muscle fibers = bulking up

  24. Atrophy is the partial or complete wasting away of a part of the body. Causes : poor nourishment, poor circulation, loss of hormonal support, loss of nerve supply, disuse or lack of exercise disease intrinsic to the tissue Atrophy is a general physiological process of reabsorption and breakdown of tissues, involving apoptosis on a cellular level. Webbed feet due to lack of aptosis wikipedia

  25. Diseases of Muscle tissue • ALS • amyotrophic lateral sclerossi • Lou Gehrig’s disease • motor neurons degenerate • Myasthenia gravis • auto-immune • antibodies to acetylcholine receptors Stephen Hawking

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