Section 15 (last section - Skeletal muscles)

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9 Terms

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What are the 3 main types of muscles?

Smooth muscle:

  • Found in internal organs and blood vessels, allow substances to travel with reduced friction

Cardiac muscle:

  • Found in the heart

Skeletal muscles:

  • Muscles attached to the bone, they work as antagonistic muscles (while one contracts, the other relaxes)

    • The contracting muscle shortens and pulls on the attached tendon

    • The tendon pulls on the bone, causing movement at joint

    • The relaxing muscle lengthens to allow movement

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Microscopic muscle structure background info:

Skeletal muscles are made from bundles of muscle fibers.

A single muscle fiber is made of specialised cell organelles (myofibrils)

<p>Skeletal muscles are made from bundles of muscle fibers.</p><p>A single muscle fiber is made of specialised cell organelles (myofibrils)</p>
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Structure of the Mycrofibril:

  • Sarcolemma - the cell surface membrane of muscle fibre

  • Sarcoplasm - The cytoplasm of a muscle fibre

  • Transverse tubules (T tubules) - Extensions of the sarcolemma that transmit electrical signals, so entire muscle recieves and contracts simultaneously

  • Sarcoplasmic reticulum - Specialised endoplasmic reticulum that is responsible for storing and releasing calcium ions

  • Myofibrils - subcellular strucutres designed for contraction

  • Multiple nuclei - skeletal muscle fibres have many nuclei because several cells merge to form one muscle fibre

<ul><li><p>Sarcolemma - the cell surface membrane of muscle fibre</p></li><li><p>Sarcoplasm - The cytoplasm of a muscle fibre</p></li><li><p>Transverse tubules (T tubules) - Extensions of the sarcolemma that transmit electrical signals, so entire muscle recieves and contracts simultaneously</p></li><li><p>Sarcoplasmic reticulum - Specialised endoplasmic reticulum that is responsible for storing and releasing calcium ions</p></li><li><p>Myofibrils - subcellular strucutres designed for contraction</p></li><li><p>Multiple nuclei - skeletal muscle fibres have many nuclei because several cells merge to form one muscle fibre  </p></li></ul><p></p>
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Myofibrils are made of many repeating units …

Myofibrils are made of many repeating units called sacomeres.

Each sacomere:

  • Thin filaments (two actin filaments with tropomyosin)

  • Thick filaments (two myosin filaments bundled together with many others)

<p>Myofibrils are made of many repeating units called sacomeres.</p><p>Each sacomere:</p><ul><li><p>Thin filaments (two actin filaments with tropomyosin)</p></li><li><p>Thick filaments (two myosin filaments bundled together with many others)</p></li></ul><p></p>
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The steps for sliding filament mechanism:

  1. Calcium ions released by the sacroplasmic reticulum causes the tropomyosin to move away from the actin binding sites.

  2. The myosin head then attaches to one of the binding sites on actin (actinomyosin bridge)

  3. ADP and Pi are released from the head, causing a power stroke where myosin head moves actin to M line

  4. The myosin head binds to new ATP molecule and dettaches from actin

  5. Myosin head hydrolyses the ATP and returns to starting position

<ol><li><p>Calcium ions released by the sacroplasmic reticulum causes the tropomyosin to move away from the actin binding sites.</p></li><li><p>The myosin head then attaches to one of the binding sites on actin (actinomyosin bridge)</p></li><li><p>ADP and Pi are released from the head, causing a power stroke where myosin head moves actin to M line</p></li><li><p>The myosin head binds to new ATP molecule and dettaches from actin</p></li><li><p>Myosin head hydrolyses the ATP and returns to starting position</p></li></ol><p></p>
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The proof of sliding filament theory:

  • The I band and H zone shorten due to an increased overlap of actin and myosin filaments

  • The A band remains at constant length, as the myosin filaments remain stationary

<ul><li><p>The I band and H zone shorten due to an increased overlap of actin and myosin filaments</p></li><li><p>The A band remains at constant length, as the myosin filaments remain stationary</p></li></ul><p></p>
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How do the calcium ions find their way into tho the myofibril?

  • Action potential arrives at the end of neurone

  • Triggers opening of calcium ion channels and calcium ions enters the neurone

  • The acetylcholine vesicles release their contents into the synaptic cleft

  • Acetylecholine diffuses across the synaptic cleft

  • Acetylcholine binds to the receptors on sarcolemma leading to opening of sodium ion channels

  • This results in depolarisation of sarcolemma.

  • The depolarisation extends through the T tubles, which interact with sacroplasmic reticulum and release calcium ions into the sacroplasm.

<ul><li><p>Action potential arrives at the end of neurone</p></li><li><p>Triggers opening of calcium ion channels and calcium ions enters the neurone</p></li><li><p>The acetylcholine vesicles release their contents into the synaptic cleft</p></li><li><p>Acetylecholine diffuses across the synaptic cleft</p></li><li><p>Acetylcholine binds to the receptors on sarcolemma leading to opening of sodium ion channels</p></li><li><p>This results in depolarisation of sarcolemma.</p></li><li><p>The depolarisation extends through the T tubles, which interact with sacroplasmic reticulum and release calcium ions into the sacroplasm.</p></li></ul><p></p>
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The three types of ATP sources from muscles

  • Aerobic respiration: when the ATP demand matches the oxygen and glucose supply

  • Anaerobic respiration: when the ATP demand does not match the oxygen and glucose supply

  • Phosphocreatine + ADP → Creatine + ATP: when the ATP demand does not match the oxygen and glucose supply

<ul><li><p>Aerobic respiration: when the ATP demand matches the oxygen and glucose supply</p></li><li><p>Anaerobic respiration: when the ATP demand does not match the oxygen and glucose supply</p></li><li><p>Phosphocreatine + ADP → Creatine + ATP: when the ATP demand does not match the oxygen and glucose supply</p></li></ul><p></p>
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The difference between slow-twitch and fast-twitch muscles:

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