LG 1.3 - Skeletal Muscle Phys Flashcards
Contraction of Sarcomere
- Myosin heads move against actin filaments 2. sarcomere gets shorter as myosin and actin move against each other 3. Z disks get closer together as sarcomere contracts
Outline the excitation-contraction coupling
- Motor neuron in anterior (ventral) horn of spinal cord send action potential through axon to motor end plate 2. Depolarization at motor end plate generates action potential in muscle 3. Sarcolemma depolarizes 4. Depolarization transfers down transverse tubules 5. DHP receptor on T-tubule undergoes conformational change in response to depolarization 6. Causes ryanodine receptor in SR to open and Ca2+ flows out
Locate and describe the Dihydropyridine receptor (2)
- located in T-tubules 2. L-type Ca2+ channel 3. Mechanically coupled to ryanodine receptor in SR –> when DHP recetpor is depolarized, the ryanodine receptor channel is activated and the Ca2+ flows out of the sarcoplasmic reticulum
Locate and describe the Ryanodine receptor channels (2)
- located in SR 2. opening of channel allows for Ca2+ to be released from SR 3. Ca2+ release allows for muscle contraction
Troponin I
strong affinity for actin
Troponin T
strong affinity for Tropomyosin
Troponin C
strong affinity for Ca2+
Explain Ca2+ role in excitation-contraction coupling
Ca2+ binds to troponin, which leads to a conformational change in the tropomyosin and exposes myosin binding sites on the actin
Cross-bridge cycling steps (4)
- ATP binds myosin head, which dissociates the actin-myosin complex 2. Myosin head is in the released state, ATP is hydrolyzed (to ADP + Pi) causing myosin to return to resting conformation (cocked state) 3. Myosin head binds to new position on actin and cross- bridge forms 4. Phosphate is released, which causes the myosin head to change confirmation, resulting in power stroke as the filaments slide past one another 5. ADP is released and myosin head is in attached state with actin
SERCA (3)
- Sarcoplasmic and endoplasmic reticulum Ca2+ ATPase 2. Pumps Ca2+ back into SR
Calsequestrin, Calreticulin (3)
Ca2+ binding proteins in the SR
Describe the Electrical component of Excitation-Contraction Coupling (5)
propagation of an action potential through the muscle
Describe the Chemical component of Excitation-Contraction Coupling (5)
release of Ca2+ from the sarcoplasmic reticulum
Describe the Mechanical component of Excitation-Contraction Coupling (5)
development of tension in the muscle fiber
Isometric Contraction
- Muscle length does not change as muscle is active 2. Maximum isometric tension is at optimum muscle

Isotonic contraction
same load, changing muscle lengths

Twitch
A single action potential through the muscle will yield a given amount of Ca2+ release. That Ca2+ release will cause a contraction in the muscle = a twitch
Tetanus
If the action potentials are at a high enough rate, the twitches will start to fuse. Fused tetanus is the state where the muscle does not have a chance to relax.
Fast twitch muscle fibers
- white, type II 2. extensive sarcoplasmic reticulum, more active enzymes that promote rapid release of energy
Slow twitch muscle fibers
- red, type I 2. more oxidative metabolism, myoglobin (iron containing substance similar to hemoglobin, combines with oxygen and stores it, this speeds oxygen delivery to mitochondria)
Locate and define the Sarcomere (1)
basic contractile unit, that is delineated by the Z disks
Locate and describe what composes the A band (1)
located in the center of the sarcomere and contain the thick (myosin) filatment
Locate and describe what composes the I band (1)
located on either side of A band, contain thin (actin) filaments, intermediate filamentous proteins, and Z disks NO THICK FILAMENTS
Locate and describe what composes the Z disks (1)
run down the middle of each I band, delineate the ends of each sarcomere