Muscle Structure and Contraction Flashcards
What types of muscle are ‘striated’?
skeletal muscle or ‘voluntary muscle’ looks banded or ‘striated’ under a microscope
heart muscle is also striated but is not voluntary
where do we find smooth muscle?
organs - note that it’s not striated muscle, it’s smooth muscle
skeletal muscles are surrounded by a connective tissues called the …..?
endomysium

muscle cells are grouped in fascicles surrounded by … ?
perimysium

Fascicles are grouped together to form the muscle which is surrounded by… ?
epimysium

what percent of body weight is made up of skeletal muscle?
40% of body weight
how would you describe the structure of skeletal muscle?
multinucleate syncytial structure = the whole thing contracts at once, it’s not seperated in function
Describe on the photo below what we’re looking at

- thick filaments, with thin overlapping them.
- A band (just where they overlap) and that creates a ‘dark’ bank
- either side of the A band you have thin filaments ( so it looks light in color)
- the Z line bisects the I band, acts as an anchoring structure holding the thin filaments together
- notice the A band where there is an overlap - the thin filaments overlap to some extent but they don’t come into the middle.
- The H zone is a light band in the middle where the Thick filaments solely exist ( no thin overlap) -
- Also in the middle of the H zone (not shown on the diagram) = M line - giving the thick filaments a certain amount of achoring.
- This whole thing is a sarcomere- which is repeated over and over again in the cell - the Sarcomere is the unit between two Z lines.

The Z band bisects what structures?
thin filaments
the M line bisects the….?
H zone (middle of sarcomere)
the H zone is in the middle of what zone?
the A zone
the M and Z band hold the thick and thin filaments together - what are these bands composed of?
they are accessory proteins - which maintain the structure such as alpha -actinin which maintains the actin lattice and dystrophin which anchors actin filaments to the sarcolemma
Patients with a deficiency in dystrophin… what happens?
their accessory proteins which hold together the thick and thin filaments cannot anchor the actin filaments to the sarcolemma - leads to destruction of the muscles
the action potential is carried through what structure in the muscle cell?
the ‘transverse tubule’ which is a sarcolemma - carries the action potential into the interior of the cell
does the sarcoplasmic reticulum share a membrane with the transverse tubule?
no the sarcoplasmic reticullum is an intracellular organelle - so even though the membrane is very close to the transverse tubule, they are seperate membranes -
how does an action potential cause the terminal cysterna to release Ca2+?
it’s the RyR (ryanodine receptor Ca2+ channel) and DHPR (dihydropyridine receptor) - when the action potential is detected by the DHPR, you get a conformational change and the RyR opens (a calcium channel) because they are physically linked and calcium is allowed to rush into the sarcoplasm (down its concentration gradient)

how many triads are in each sarcomere?
each sarcomere has two triads (triads are a source of calcium)
the cross bridges are conveniently located by what structure?
they are conveniently located near the triads (which are the sarcomere’s source of calcium)
what part of myosin forms the bridges between thick and thin filaments?
the myosin head - forms bridges - these heads stem from the thick filaments

what proteins are associated with the thin filaments?
troponin and tropomyosin

the sarcomere is a unit of myofibril contained between what two lines?
the Z lines
in skeletal muscle, triads are located at the junction of which two bands?
triads are located at the junction of the A and I bands
describe how an action potential propagates and leads to muscle shortening
- Na+ entry initiates an action potential which is propagated along the sarcolemma and down the T tubules
- action potential in the T tubule activates voltage sensitive receptors which in turn trigger Ca2+ release from terminal cisternae of SR in cytosol
- caclium ions bind to troponin- troponin changes shape, removing the blocking action of tropomyosin (pulls the tropomyosin deep into the groove of the filament which exposes the active site) actin activates sites exposed
- contraction- myosin heads alternatively attach to actin and detach, pulling the actin filaments toward the center of the sarcomere - release of energy by ATP hydrolysis powers the cycling processes
- removal of Ca2+ by active transport into the SR after the action potential ends
- tropomyosn blockage restored, blocking myosin binding sites on actin - contraction ends and muscle fiber relaxes
