lecture1 muscle physiology-3

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    Muscle Physiology

    Modul: Nervesystemet ogbevægeapparatet

    Learning Outcomes

    1. Describe the relationship between structureand function of the skeletal muscle fibre.

    2. Describe the events leading to muscle fibrecontraction.

    3. Describe the biochemistry of forcegeneration.

    4. Describe the length-tension relationship.

    5. Describe the role of the intramuscularconnective tissue framework.

    Muscle types Smooth Cardiac Skeletal / Striated

    Limb muscles generally have 2 attachmentpoints – origin & insertion

    Outer connective tissue layer of muscle(epimysium) is continuous with the tendonwhich in turn attaches to the fibrousconnective tissue of bone (periosteum)

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    Skeletal Muscle

    Machines that convertchemical energy tomechanical work & heat

    Muscles withgreater pennationangles have moresarcomeres inparallel and fewerin series.

    Thus better able togenerate force butnot so greatshorteningvelocities..ie. Nogood for speed

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    Single muscle fiber enclosed

    by endomysium – anextension of the sarcolemma

    One muscle fiber is approxas thick as a strand of yourhair!

    Under the microscope it hasa “striated” appearance

    Many fibers (up to 150)bundled together = fasiculus

    Fasiculus enclosed byperimysium

    Many fasicles bundledtogether & enclosed byepimysium = one muscle

    Basic Structure

    Basic Structure

    Important

     All the connective tissue – epimysium,perimysium, andendomysium iscontinuous with thetendon

    Thus any tensiondeveloped in onemuscle cell istransmitted to thetendon.

    Under theMicroscope

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    Myofibrils – what you cannotsee

    approx 100’s - 1000’smyofibrils = one musclefiber

    1/100th size of a strandof your hair

    Contain the apparatusthat contracts themuscle cell

    approx 4500sarcomeres per cm ofmuscle

    More of what you cannotsee:

    The smallest functionalunit is the sarcomere

    2.2microm

     Actin & Myosin filaments(proteins) arrangedlongitudinally

     Actin6nm diameter – thin

    filaments – double helix

    Myosin16nm diameter (1/10,000

    of hair strand)

    Cross bridges protrudefrom myosin molecule

    Sacroplasmic reticulum & T-tubules

    SR – intricate system oftubules – terminates asvesicles close to Z-lines(line btw 2 sacromeres)

    Calcium ions stored invesicles

    Regulation of calciumregulates muscularcontraction

    T-tubules run to 2 SRvesicles

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    The Motor Unit

     A motor neuron + allthe muscle fibers it

    innervates =MOTOR UNIT

    The Motor Unit

    So what happens when a nerve axon

    excites the muscle fibers of a motorunit???

    The NeuromuscularJunction

     ACh diffuses acrosssynaptic cleft &attaches toreceptors onsarcolemma

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     At SR & T-Tubules:

    Initiation of muscleaction potential (MAP)

    The MAP depolarizestransverse tubules at A-I junction of sarcomere

    Calcium release fromlateral sacs ofsarcoplasmic reticulum

    Ca2+ ions bind to troponin-tropomyosin in actin filamentsthus freeing actin to bind withmyosin

     Actin combines with myosin- ATP. It also activates mysosin – ATPase which splits ATP.Energy thus released producesthe movements of the myosincrossbridge, thus tension iscreated.

     ATP binds to myosin bridge

    breaking actin-myosin bond,thus actin-myosin slide pasteach other (muscle shortens)

    This process is repeated whileCa2+ concentration is high

    The slidingfilament theory

    a muscle shortens orlengthens because thethick (myosin) and thin(actin) filaments slidepast each other withoutactually changing length

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    Sarcomere: number of attached cross-bridges, degree of overlap

    Length-Tension Relationship

    the force a muscle can produce depends on the amount ofactin-myosin overlap – ie. the muscle length

    Types ofmuscle

    contraction

    Types ofmuscle

    contraction

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     ATP – The energy currency

     Adenine: nitrogencontaining base

    Ribose: a 5 carbonsugar

    Most important arethe 3 phosphategroups!

    Removal of 1 byhydrolysis = ADP

    Removal of anotherone = AMP

     ATP – The energy currency

     ATP is ESSENTIAL if we are to performany movement

    Where then does it come from?

    Some is stored directly in muscle cell but

    this is not much [5mmol], thus we haveto constantly produce ATP!

    How?

    Biological Energy Systems

    The replenishment of ATP in human skeletalmuscle is accomplished by 3 basic energysystems:

     – Phosphagen System

     – Glycolytic System

     – Oxidative System

     All 3 are active at any one time, BUT, theextent to which each is used DEPENDS intensity of activity & duration of activity

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    Phosphagen System

     Active at start ofactivity regardless ofintensity

    Provides ATPprimarily for short-term, high-intensityactivities

    Limited amounts of ATP & creatinekinase are stored!

    Phosphagen System

       ADP concentration = activity of Creatine Kinase

       ATP concentration =

    activity of Creatine Kinase

    Immediately at start of exercise this system is used, thus: ATPproduced &  ADP concentration, thus activity of CreatineKinase. IF exercise stops or is at a low enough level for othersystems to kick in then  ATP concentration & activity ofCreatine Kinase

    Phosphagen System

    Provides an immediate source of ATP

     AMP stimulates glycolysis!!!!!

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    Glycolytic System

    Glycolysis = breakdown ofcarbohydrates to produce ATP

     – Glycogen stored in muscle, or

     – Glucose delivered in blood

    Multiple reactions involved - nxt pg

    Glycolysis – fast vs slow

    LACTATE There is no such thing as LACTIC ACID! only

    LACTATE – this is what you measure whenyou take blood samples! It is NOT linked tofatigue!!!!

    Clearance of lactate from blood reflects aperson’s ability to recover

     – Both aerobically & anaerobically trained individualsclear lactate FASTER than untrained

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    Biological Energy Systems

    Biological Energy Systems

    Substrate Depletion & Repletion

    Energy substrates – molecules that providestarting materials for bioenergetic reactions –phospagens (ATP, creatine phosphate),glucose, glycogen lactate etc etc

    Depletion = ability to produce energy

    Fatigue associated with substrate depletion

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    Substrate Depletion & Repletion

    Phosphagens Depletion:

     – Creatine phospate depleted by 70% during first 30s ofintense exercise

     – ATP never fully depleted – 60% during high intensityexercise

    Repletion: – CP within 8 mins post exercise – ATP within first 3-5 mins

    Training effect: –   storage within muscle cell? - uncertain –   muscle mass = storage within whole muscle – resistance

    training but also sprint training

    Substrate Depletion & Repletion

    Glycogen Depletion:

     – Limited stores in muscles & liver – these can be controlledby diet

     – Rate of depletion depends on exercise intensity – liverglycogen rarely depleted

     – High intensity, intermittent exercise e.g. resistance trainingcan cause substantial in muscle glycogen stores

    Repletion:

     – Related to post exercise carbohydrate ingestion. – Approx 24hrs required

    Training effect: –   storage through anaerobic training e.g. sprinting &

    resistance but also aerobic training

    Metabolic specificity of training

     Appropriate exercise INTENSITIES & REST intervals can permitthe “selection” of specific energy systems during training forspecific athletic events.

    Most sports have various “metabolic” demands i.e. they arecomprised of a series of high intensity, constant or nearconstant effort interspersed with rest periods

    Pure aerobic training is NOT effective!

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    The end