Muscle Flashcards
What type of PNS innervation are the 3 types of muscle cells?
Skeletal= somatic motor Cardiac= involuntary automatic nervous system control Smooth= involuntary automatic nervous system control
- What does skeletal muscle look like on a slide?
2. Difference between cardiac and smooth muscle on a slide?
- Many muscle cells are fused together
- Cardiac cells are separated by intercalated discs; smooth cells are separated by ECM (on slide, cardiac looks like there is more white spots - glycogen)
Hierarchical levels of organization of skeletal muscle? (From big to small)
Muscle fascicles, muscle fiber, myofibril, sarcomere
3 connective tissue layers that surround and subdivide skeletal muscle?
What do these connective layers contain?
Epimysium, perimysium,
Endomysium
Blood vessels and nerves supplying muscle cells
When staining a skeletal muscle slide, which type of fiber looks darker?
Dark staining = slow twitch fibers
Light staining = fast twitch fibers
Function of the sarcoplasmic reticulum?
Ca2+ storage site; releases Ca2+ into cytoplasm when muscle is activated
What is a triad?
Cell membrane of muscle cell forms T tubules arranged in parallel with sarcoplasmic reticulum (terminal cisterna) — triads can cause the SR to release its Ca2+
muscle contraction: Inside a myofibril, two major types of proteins are anchored at the ___
Z line
Thick filaments = ?
Thin filaments are combination of 3 things = ?
Which ones are anchored to the Z line?
Thick = myosin Thin= actin, tropomyosin and troponin
Thin
What causes skeletal muscle to appear striped (striated)?
Sarcomere
Sarcomere extends from the ___ (location)
What is dystrophin?
Z line which is linked to the sarcolemma
A protein that links the Z line to the cell membrane
What is happening in muscle contraction?
Thick and thin filaments pull on each other to shorten the sarcomere and entire muscle
Myosin has a head and tail, significance?
Myosin heads have binding sites for actin, ATP, and ATPase
What does the enzyme ATPase do?
Releases energy by converting ATP to ADP + Pi
Function of troponin?
Can bind tropomyosin and Ca2+
Steps of the cross bridge cycle (sliding filament model)
~Before cycle starts, troponin blocks myosin head~
Activation of muscle cell leads SR to release Ca2+
Ca2+ binds to troponin, leading it to expose the myosin head for actin to bind to
ATP binds to myosin head, causing actin to detach
ATP gets broken down and energy is released causing conformational change in myosin head
POWER STROKE= unbinding of Pi leads to strengthened binding of actin, which pulls on the thin filament thus shortening the sarcomere
After power stroke step, how does another contraction start or cycle stop?
When no ATP is present, the myosin will remain attached to then actin (so unable to start another contraction) (rigor mortis)
So what two things are necessary for muscle contraction?
ATP and Ca2+ release
Neural input steps in order to get to the start of the cross bridge cycle?
Nerve impulse triggers release of acetylcholine into synaptic cleft
Acetylcholine binds to ionotropic receptors (Na+ channels) allowing Na+ to enter the cell thus increasing voltage
The voltage change causes Ca2+ release from SR into cytoplasm
What is another name for an axon terminal?
Bouton
So overall, release of ___ leads to Ca2+ release
Acetylcholine
Clinical correlation: Myasthenia Gravis
- Pathophysiology?
- How does it present?
- Diagnostic tests? Will see improvement upon administering?
- Antibodies are generated against nicotinic acetylcholine receptor
- Muscle weakness (at first muscle strength will seem the same, but muscle will fatigue much quicker than it should)
- Detection of nAchR antibodies; administration of acetycholinesterase inhibitor (edrophonium)
- Muscular Dystrophy (Duchenne and Becker Types) is caused by what?
- More common in boys or girls? How does it present?
- Difference in onset and progression of Duchenne vs Becker
- Mutations of dystrophin gene
- More common in boys (X linked); presents as weakness after achieving motor milestones (crawling, standing, walking, etc.)
- Duchenne- 3-5 years old, much more rapid progression (inability to walk by 12)
Becker- 12 year old onset, slower progression (unable to walk by 25)
Two sensory structures of skeletal muscle and what they sense?
Muscle spindles- sense muscle stretch
Golgi tendon organs-sense contraction