L5: Physiology of Muscle Contraction Flashcards

1
Q

how does troponin work

A

1) 4 calcium ions bind to troponin C
2) in heart TnC only binds to 3 Ca2+
3) causes troponin to change its conformation
4) Conformational changes in troponin shut off TNI
5) Tropomyosin-troponin leaves F-actin groove and unmasks the myosin binding site on actin
6) Next myosin heads make cross bridges cycling to actin
7) myosin breaks down Atp
8) myosin pulls thin filaments

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2
Q

what does the significance of the total TNI marker

A

Total TnI = marker for total muscle breakdown

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3
Q

what does the cardiac TNI signify

A

Cardiac TnI = marker for myocardial infarct

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4
Q

describe cross bridge cycling

A

contraction depends on the binding of myosin heads to thin filaments at specific sites

-In resting state of sarcomere, myosin heads are blocked from binding to actin by tropomyosin

this occupies the specific binding sites -( in F-actin double helical groovwe)

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5
Q

describe the relationship between force generation and sarcomere length (study slide 7)

A

-Increase in overlap of thick and thin filaments provide an increase in force

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6
Q

core memorisation of cross bridge cycling

A

1) myosin releases actin
2) myosin head cleaves ATP
3) Myosin head binds actin
4) power stroke performed

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7
Q

what occurs in rigor mortis

A
  • Atp depleted after death
  • muscle cell does not requester ca2+ into SR, so increase in cytosolic ca2+
  • Ca2+ allows cross bridge cycle contraction until ATP and creatine P runs out
  • w/O ATP- myosin stops just after power stroke, so actin still bound to myosin, and this ends when muscle tissue degrades in 3 days
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8
Q

Info on creatine

A

1- creatine found in muscle fibres

2- Phosphorylated to creatine phosphate

3- this is how energy is stored in the muscle

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9
Q

what occurs to creatine phosphate during cross cycling

A

When cross bridge cycling hydrolyses ATP to ADP + pi, creatine phosphate donates a high energy phosphate to ADP restoring it to ATP

ATP levels must be kept stable - buffering and regeneration

the reaction is catalysed both ways by creatine phosphokinase

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10
Q

difference between creatine and creatinine

A

Creatine is a small molecule that can accept high energy phosphate bonds from ATP

  • creatine-phosphate is the above molecule after phosphate has been added to it

-creatinine is a diagnostic marker for kidney function
and is the breakdown product of creatine

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11
Q

what is CPK a biomarker for

A

Muscle destruction

detected by antibodies

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12
Q

describe the calcium gradients

A

there are 2 calcium gradients;
- extracellular vs cytosolic free calcium

  • SR vs cytosolic free calcium

It is the efflux of calcium from the SR to the cytoplasm that provides most of the calcium

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13
Q

the depolarisation of muscle

A

1- ACh leads to muscle depolarisation

2- active nicotinic AChR leads to net inward current

3- depolarisation spread via T-tubules

4- local action potentials trigger calcium efflux from terminal cisternae across membrane of sarcoplasmic reticulum into fibre cytoplasm

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14
Q

describe E-C coupling

A

Ryanodine receptor (RyR)

in SR membrane releases ca2+ from SR triggered by voltage sensor on ca2+ channel

SERCA in SR membrane pumps ca2+ back into SR and requires ATP

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15
Q

what is the molecular basis of tetany

A
  • single AP leads to calcium release from SR which leads to twitch
  • Ca2+ ions are rapidly pumped back into SR leading to the end of twitch
  • Frequent Aps lead to insufficient calcium resequestration and summation of contraction
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16
Q

study slide 16

A

how was it

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17
Q

what are the 2 main types of muscle fibres

A

1- slow twitch (type 1 red oxidative, small diam, )

high myoglobin, many mitochondria

2- fast twitch (type 2 white- non- oxidative wide diam lower myoglobin, increases energy from glycolysis

18
Q

what are the differing properties of the fibres

A
  • aerobic vs anaerobic
  • faster calcium reuptake
  • maximum tension produced

fatigue resistance

19
Q

what are the basis of muscle fibre type

A

Slow -fast

type 1 2A 2X 2B

20
Q

how are the fibre types distributed -ie

A

Soleus= 80% type 1 (slow), 20% type 2A

vastus lateralis = mixture of type 1 2A and 2X

21
Q

study slide 20

A

how was it

22
Q

what are the 3 types of muscle coordination

A

Motor Units
Recruitment & size principle

Tetany

Fusion of myocytes into long myofibres

23
Q

define motor units

A

a single alpha motor neuron and all muscle fibres it innervates

functions as a single contractile unit of skeletal muscle

all muscle fibres in a single motor unit are of the same type

24
Q

describe motor units in large muscles

A

-responsible for large muscle contractions that are powerful and synapse onto 1000 fibres

25
Q

describe a small muscle motor unit

A

Mediate precision movement- synapse onto 2/3 muscle fibres

26
Q

what does the type and function of the lower motor neuron determine

A

The muscle fibres

27
Q

what is isometric contractile force generation

A

generates a variable force while length of muscle remains unchanged

28
Q

isotonic force generation?

A

generates a constant force while the length of the muscle changes

29
Q

describe the sequence for force generation in muscle fibre

A

stage 1 : isometric- force increases, joint doesn’t move, as muscle force - force increases -ie biceps and brachioradialis

stage 2: isotonic : force remains the same, arm moves, glass moves upward in response to force- overcoming gravitational and inertia forces keeping glass on table

glass starts to rise as muscles shorten and the elbow bends and force generated by the muscle is constant as glass moves

30
Q

what are the types of muscular force generation

A

Concentric- force during contraction - tossing a ball into air

eccentric: force during muscle elongation - catching a ball

31
Q

what controls force generation

A

proprioception

32
Q

what is the recruitment size principle

A

As the initial contraction occurs, more and more motor units are recruited starting with smaller ones and progressively adding larger ones

allows fine graduation of force for small movements

until it becomes contraction=isotonic

33
Q

what is the difference between upper and lower MND

A

LMND :

  • weakness
  • muscle atrophy

UPMND:
spasticity and hypertonia

34
Q

describe and give an example of a stretch reflex

A

Patellar reflex which functions for posture and balance

it controls muscle length and increases muscle force

35
Q

what fibres are in sensory organs

A

intrafusal fibres

36
Q

what fibres ae in traction organs

A

Extrafusal fibres

37
Q

what does a lack of patellars reflex cause

A

westphals sign

38
Q

describe spindle

A

A spindle consists of 3-12 intrafusal fibres
Gamma motor neurons increase sensitivity
Drive contraction of edge of intrafusal fibres
Sensors from muscle spindle are:
Called Type 1a and Type 2
Wrap around the intrafusal fibres
Detect stretch (ie length) of central non-contracting region using stretch receptors
Spindle is like a thermostat that regulates the relationship between muscle length and muscle contractility
ie the relationship between neural drive and force generation

39
Q

what does westphels sign mean clinically

A

Receptor damage
Femoral nerve damage
Peripheral nerve disease
e.g. Peripheral Neuropathy

In upper motor neuron disease
Can lead to hypertonia and spasticity
UMN inhibits normal descending inhibitory input to spinal interneurons
The spindle reflex becomes over-sensitive
Can attempt to contract muscle all the time

40
Q

what is the tendon reflex

A

Decreases Muscle Force  dropping the load
Sensor firing -  less- contraction

Sensor to Spinal Cord

Interneuron to motor neuron

Motor neuron inhibited

Motor neuron to muscle

41
Q

give examples of a tendon reflex

A
Sensor = Golgi Tendon Organ
Detects Tension
In series with muscle
In tendon
Near border with muscle

Disynaptic
Ipsilateral Spinal reflex

42
Q

give an example of patellar stretch reflex

A

Detects Stretch
i.e. Length
Proprioception

Spindle is Parallel to other muscle fibres

Ipsilateral Spinal reflex

Monosynaptic