Muscle Flashcards
What do skeletal muscle differentiate from
Mesenchymal cells
Skeletal muscle development
- Myoblasts align and fuse to make multinucleated myotubes
- Myotubes synthesize myofilaments; cross-straitions gradually begin to appear
- Myotubes continue to differentiate into myofibrils
Endomysium
- Thin Reticular fibers
- Supplies fascicles with nerves and capillaries
Perimysium
CT (collagen) layer surrounding fascicles
Septa
- Between fascicles
- Carry nerves, blood vessels and lymphatics
Epimysium
-Dense irregular CT
Myotendinous Junction
- Between muscle and tendon
- Tendon is dense collagen
Myofilaments
Actin and myosin
-Arraged into sarcomeres
A-bands
Ansiotropic/birefringent in polarized LM
-Myosin
I bands
Isotropic
-Actin
Thin filaments contain
F-Actin and G-actin, tropomyosin, and troponin
Sarcoplasmic reticulum has high amount of which organelle
Mitochondria
Muscle Contraction
- Nerve impulse triggers Ach release
- Ach binds nicotinic receptors in motor end plate
- Impulse travels down sarcolemma and t-tubule
- Ca release from SR
- Ca binds troponin, moves trypomysin out the way
Muscle contraction at myosin head
-Attach, powerstroke, detatch, return
Myasthenia Gravis
- Autoimmune disorder
- circulating antibodies bind to Ach receptors, interfering with EPP
- Leads to skeletal muscle weakness
- Extraocular eye muscles are easily affected, causing diplopia (double vision) early sign
How does body attempt to combat myasthenia gravis
- Junctional folds with affected receptors are internalized, digested by lysosomes, and replaced
- However, this doesn’t last long, bc antibodies attack again
Early sign of myesthenia gravis
Diplopia (double vision) bc extrinsic eye muscles affected
Muscular dystrophy types and similarities
Duchenne muscular dystrophy and Becker muscular dystrophy
- Both X-linked mutations of the dystrophin gene, more common in boys
- Childhood onset: weakness begins after a delayed onset, develops after achieving motor milestones
Dystrophin
-Connects the Z-line to both the sarcolemma and ECM, giving stability to myofibrils
Duchenne Muscular Dystrophy
- Weakness occurs at 3-5 y/o
- Disease progresses rapidly
- Loss of fxn by 12
- May become dependent on assisted breathing
Becker Muscular Dystrophy
Later onset (12 y/o)
- Slow progression
- Loss of fxn before 30
LM appearance of Muscular Dystrophy
- Fat replaces muscle
- Hypertrophy and atrophy of some fibers
- Dystrophin disruption
Muscle spindles
- Encapsulated by modified perimysium
- Contain intrafusal fibers
- Intrafusal fibers are modified muscle fivers
Golgi Tendon
- Provide sensation of body position and maintain muscle tone
- Responsible for proprioception, reflexive inhibition, and activation of opposing muscles