Mechanism Of Muscular Contraction Flashcards

1
Q

organize the structure of muscle

A

Contractile protein filaments are tethered within myofibrils –> myofibers or cells–> fascicles –> muscles

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2
Q

how does adult muscle growth occur

A

Adult muscle growth from some fusion of satellite cells into fibers, but mostly from synthesis of new myofibrillar proteins

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3
Q

differentiate embryonic, neonatal and adult myogenesis

A

embryonic forms the primary myogeneis which fuse to form the synthesis of new myofibrillar proteins forming scaffolds

neonatal is responsible for establishing the stellate cell niche as well as adult fiber type specification

adult is where the BM is assembled and you get the formation of the NMJ

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4
Q

what is the significance of the I band

A

the region where the thin filaments are not super imposed by the thick ones

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5
Q

what protein is responsible for tethering the thick and thin filaments

A

titin

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6
Q

which fibers (I or II) have the most myoglobin content?

which fibers are largest

which one are the most red in color

A

fiber type 1

fiber type II are twice as large

fiber 1 due to myoglobin (IIb stain the lightest)

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7
Q

what kind of channel is the receptor on the motor end plate

A

NA/K pump which pumps Na in and K out

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8
Q

which part of the NMJ does the esterase lie

A

motor end plate

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9
Q

what antiporter is responsible for the activation of the ACH release

what symporter is responsible for the activation of the ACH release

A

Ca- ACH release from presynaptic terminal

NA on the presynaptic terminal

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10
Q

what is the reason for latency phase in the electrochemical signaling of the NMJ

A

Latency due to time needed for Ca2+release from SR

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11
Q

how does the requires stimulus to fire change with the fiber size

A

smaller fibers are from small motor units and they require less stimulus to fire…. also remeber that the fast twich fibers are larger

the integrated of multiple fiber types allows graded contractile response

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12
Q

define fiber summation versus frequency summation

A

fiber summation Motor units may be recruited according to size, leading to stronger contraction

frequency summation Repeated stimulation at frequencies that do not allow time for sufficient calcium reuptake will produce stronger contraction with each stimulus (frequency summation) and result ultimately in a state of sustained contraction (tetanus/tetany)

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13
Q

what allows muscles to maintain constant tension

A

alternate firing of the motor units

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14
Q

describe the electrochemical basis for skeletal muscle contraction

A

depolarization activated the voltage-gated calcium channel, the dihydropyridine receptor (DHPR)–> brings in ca which then activates RYR1 (CSCR) on SR = release of ca into cytosole and into T tubule from SERCA = contraction

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15
Q

what stores the SR calcium

A

SERCA

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16
Q

What is the cascade of events that take place for a muscle to fire

A

Nerve AP

nerve release

muscle AP

muscle relase of Ca from SR

muscle contraction

17
Q

what does the interaction of sliding filaments produce

A

cross bridge cycling

18
Q

name something that helps the filaments in the myosin actin complex stay tethered in close proximity

A

myosin-binding protein C

19
Q

how does contraction occur on the molecular level

A

this cross bidge cycling is ATP dependent and Ca regulated

ATP binding decreases the affinity

1- ATP binds to myosin and reduces its affinity for actin, allowing release of the rigor state.

2- Once ATP binds, it is hydrolyzed to ADP and a phosphate, both of which remain bound to the myosin head.

3- Once calcium becomes available, it binds troponin C and causes the conformational shift in tropomyosin that will allow actin-myosin binding.

4- The weak initial binding of actin and myosin in the presence of calcium triggers release of the phosphate residue –> concomittent strong binding of actin/myosin and triggers a power stroke.

3- ADP is released during the power stroke as well, leaving the myosin bound once more to actin.

Removal of calcium leaves myosin and actin chains bounds together until the next ATP binds the myosin head. This completes the cycle, and means we have now described both electrochemical and physiochemical properties of skeletal muscle that allow the cross bridge cycling that we see as muscle contraction, and have completed the excitation contraction coupling that ties the electrical, chemical, and mechanical responses in skeletal muscle.

If no ATP is present, the bound myosin retains its high affinity for actin, and will remain locked to it in a state of rigor. This is not likely to happen in a living being, as ATP levels are tightly managed and ATP is thus available.