Module 5-Midterm- Muscles Flashcards

1
Q

What are the three types of muscles?

A
  • skeletal: primarily for voluntary motion
  • cardiac: found in the heart
  • smooth: walls of blood vessels, airways, ducts, bladder, uterus and digestive tract
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2
Q

What is the purpose of muscles?

A
  • movement
  • heat production
  • body support and posture
  • 600 diff muscles in the body
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3
Q

Structure of the muscle

A
  • whole muscles are made up of bundles of fasiculi
  • each fascicle is made up of muscle cell or fiber
  • each muscle cell or fiber contains myofibrils
  • myofibrils have thick and thin filaments
  • thick myofilaments have myosin
  • thin myofilaments have actin, troponin and tropomyosin
  • fasciculi surrounded by perimysium
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4
Q

what is the sarcolemma?

A
  • surrounds muscle cell
  • muscle cell membrane
  • over where the action potential is transmitted
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5
Q

what are the transverse tubules?

A
  • tubelike projections off the sarcolemma that extend down into the cell
  • conduct action potentials depp into the cell where the myofibrils are located
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6
Q

what is the sarcoplasmic recticulum?

A
  • surrounds myofibrils

- mesh like networks of tube containing Ca ions

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7
Q

Terminal Cisternae

A
  • at either end of sarcoplasmic reticulum

- a membranous enlargement of SR

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8
Q

Thin myofilament

A
  • made of globular protein actin
  • contains special binding site for myosin
  • tropomyosin protein found here (covers binding site when muscle is at rest)
  • troponin A binds to actin
  • troponin T binds to tropomyosin
  • tropinin C binds to Ca+
  • troponin C binds to Ca+ and pulls tropomyosin off the binding site
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9
Q

Thick myofilament

A
  • myosin
  • long, bendable tail protein with two heads to attach to myosin binding site
  • also has head that can bind to ATP that releases energy to myosin that powers contraction
  • many myosin molecules arranged to make one thick filament
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10
Q

Actin/Myosin Relationship

A

-thin and thick filaments arranged in a repeating pattern
-z disk= from one Z disc to another
-m line= centre of sacromere, group of thick fila extend outward from this line
-A bands= thick filaments
-I bands= think filaments
sacromere= from one z disc to another

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11
Q

sliding filament theory

A
  • head of myosin molecule attaches to myosin binding site on actin, forms and crossbridge and the myosin changes shape
  • change in shape causes myosin head to swing, producing a power stroke
  • powerstroke slides actin passed myosin
  • thin or thick filaments DO NOT shorten during contraction
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12
Q

Excitation contraction coupling

A
  • process in which an AP in the cell membrane (sarcolemma) excites the muscle cell to produce a contraction
  • the AP generated at the NMJ will spread out over the sarcolemma, down the T tubules into the core of muscle cell
  • AP travels very close to the SR and will open Ca+ channels, causing a release of Ca+ from the terminal cisternae of the SR
  • Ca+ binds to troponin C on the thin myofilament, causing tropomyosin to uncover the myosin binding sites
  • myosin will attach to actin and the Powerstroke will occur
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13
Q

Relaxation of the muscle

A
  • once AP stops, Ca+ will no longer diffuse out of the SR
  • special Ca+ pumps rapidly pump Ca+ back into the SR (up its concentration gradient, requires ATP)
  • without calcium present in the cytoplasm of the cell, tropomyosin will cover the binding sites again, and the Powerstroke will not take place
  • muscles will not relax if there is a build up of Ca+
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14
Q

ATP cycle and muscle contraction

A
  • ATP splits to ADP and PI head, releases energy to myosin and prepares the head from activity
  • An action potential occurs, Ca+ is released from the SR and binds to troponin C. This rolls tropomyosin off the binding site on actin
  • Powerstroke occurs, and the ADP and PI are released from the myosin head
  • new ATP molecule binds to the myosin head
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15
Q

Rigor Mortis

A
  • 3/4 hours after death
  • stiffness disappears after 24-48 hrs
  • results from the loss of ATP in muscles
  • slow degradation of the SR, causes a release of Ca+
  • cross-bridge is formed, however without ATP the bonds cannot be broken (will eventually let go with cell degeneration)
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16
Q

Altering the force of contraction

A

2 methods:

     - recruiting motor units
     - summation of twitch contractions
17
Q

The motor unit

A
  • is a motor neuron and all the muscle cells/fibers it causes to contract
  • one motor neuron will contact several different muscle cells (each cell is only innervated by one motor unit)
18
Q

Recruitment of motor units

A
  • activation of more motor units

- progressive activation resulting in a stronger contraction

19
Q

muscle twitch

A
  • smallest muscle contraction
  • 1 AP in the motor neuron
  • single AP excites muscle cell, causes release of Ca from the SR
  • twitch is 10-100ms
  • AP is 2ms, there is a latent period because of all the events going on at the NMJ
20
Q

Summation of twitch contractions

A
  • increasing the number of action potentials per second traveling down the nerve
  • increasing muscle tension
21
Q

maximal tetanic contraction

A

-plateau in muscle contractions, where no more AP can be added per second