skeletal muscle physiology - finish on ipad Flashcards
myofibril structure =
a long cylindrical organelle within a muscle fibre that is highly specialised for contraction
sarcomere =
space between two Z-lines
A-band =
part of the myofibril where thick myosin filaments are present
I-band =
part of the myofibril where only thin actin filaments are present
H-band =
part of the myofibril where only thick myosin filaments are present
thin filaments =
are formed from actin in complex with troponin and tropomyosin
thick filaments =
are formed from large numbers of myosin II molecules
regulation of contraction:
Ca2+ dependent
at high calcium conc. the myosin binding site-cross bridge cycling can occur
titin:
titin forms fine filaments that stabilise the myosin filament position
titin extends from Z-disk to M-line
with muscle activation calcium binds to titin and alters its stiffness = provides increased force when muscle is stretched and resists over stretching
mechanism of muscle contraction:
- action potential arrives at neuromuscular junction, causing Ca2+ to enter the motor neurone, depolarising it = acetylcholine is released
- acetylcholine binds to sarcolemma causing Na+ diffusion, depolarising it - action potential sped up by transverse tubules
- action potential triggers Ca2+ release from sarcoplasmic reticulum, it binds to troponin on the actin filaments
- troponin changes conformation exposing binding sites
- myosin heads attach to binding sites and tilt 45 degrees (powerstroke) - ADP and Pi are released
- actin filaments are pulled passed myosin filaments (sarcomere contracts)
- ATP attached to myosin heads are hydrolysed to ADP and Pi - this energy is used to detach myosin heads from actin filaments
control of intracellular calcium in muscle is done by…
transverse tubules on the sarcolemma and sarcoplasmic reticulum
dihydropyridine receptors =
located on transverse tubules - are voltage-gated channels that sense change in membrane potential during action potentials
are coupled to ryanodine receptors
ryanodine receptors =
release calcium from sarcoplasmic reticulum into cytoplasm
coupled to dihydropyridine receptors
excitation-contraction coupling:
- End plate potential triggers action potential in muscle fibres
- Action potential propagates along sarcolemma and down T-tubules
- Depolarisation of T-tubules is sensed by dihydropyridine receptors that are couples to ryanosine receptors on sarcoplasmic reticulum causing them to open
- Ca2+ is released into cytoplasm - initiates cross bridge cycling and contraction
- Ca2+ is pumped back into sarcoplasmic reticulum (by sarcoplasmic + endoplasmic reticulum calcium ATPase) and this terminates cross bridge cycling
the cross-bridge cycle:
- Ca2+ binds to troponin on actin filaments - troponin changes conformation exposing binding sites
- myosin heads attach to binding sites and tilt 45 degrees (powerstroke) - ADP and Pi are released
- actin filaments are pulled passed myosin filaments (sarcomere contracts)
- ATP attached to myosin heads are hydrolysed to ADP and Pi - this energy is used to detach myosin heads from actin filaments