W29-L3,4: Skeletal muscle and ageing Flashcards

1
Q

In the slowest contracting are there fast twitch fibres?

A

Yes

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2
Q

What are the goal of interventions to attenuate muscle wasting?

A
  • attenuate muscle atrophy

* promote muscle strength

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3
Q

What is myostatin and what does knocking it out cause?

A

myostatin is a “negative regulator” of muscle mass and knocking out causes increase of muscle mass

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4
Q

What is disuse muscle atrophy?

A

when the muscle is not used eg loss of gravity which upsets balance of synthesis vs degradation

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5
Q

What is seen in muscle wasting in the ICU?

A

significant inflammation which upsets balance of synthesis and degradation, disruption of architecture and atrophy of muscle

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6
Q

What is sarcopenia?

A

age-associated loss of skeletal muscle mass and function

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7
Q

What is used for the diagnosis of sarcopenia?

A
  1. low muscle mass
  2. low muscle strength
  3. low physical performance
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8
Q

What type of muscle activity declines the fastest?

A

muscle activity that

requires explosive contraction

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9
Q

What is muscle weakness?

A

an inability to develop an initial force appropriate for the circumstances

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10
Q

Beyond what age is there a steep drop in muscle strength?

A

50

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11
Q

Which muscles are more protected from sarcopenia?

A

Slower muscles

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12
Q

What happens to fibres that lose their innervation?

A

They atrophy

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13
Q

What can re-innervation of muscles fibres cause?

A

Causes them to change from fast to slow fibres

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14
Q

When does slowing of contraction occur?

A

Occurs before severe muscle wasting

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15
Q

Are there neural changes in sacropenia?

A

Yes, not just muscle effects

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16
Q

How does connective tissue within muscle change with advancing age?

A

Become stiffened because they loose their elasticity due to increased connective tissue

17
Q

Are the effects of ageing on muscle reversible?

A

No, but they can be attenuated

18
Q

Are older muscles still responsive to interventions like strength training?

19
Q

What is the onset of Duchenne muscular dystrophy?

A

About 2-6 years old

20
Q

What are the symptoms of Duchenne muscular dystrophy?

A

Generalised weakness and often enlarged calves

21
Q

What is the progression of Duchenne muscular dystrophy?

A

Progresses slowly but survival is rare beyond late twenties

22
Q

What is the inheritance of Duchenne muscular dystrophy?

A

X linked recessive

23
Q

What is gowers sign?

A

Have to walk themselves up to stand up

24
Q

What causes Duchenne muscular dystrophy?

A

mutation in the dystrophin gene which causes deficiency in dystrophin expression (usually complete absence)

25
What is the role of dystrophin?
cytoskeletal protein that holds the fibres in place
26
What is the dystrophin-glycoprotein complex?
shock absorber that helps transmits forces
27
What is onset of becker muscular dystrophy?
adolescence or adulthood
28
What are the symptoms of becker muscular dystrophy?
Almost identical to duchenne but much less severe
29
What is the progression of becker muscular dystrophy?
Slowly, survival into mid to late adulthood
30
What is inheritance of becker muscular dystrophy?
X-linked recessive
31
What is the cause of becker muscular dystrophy?
Significant amounts of abnormal smaller dystrophin molecules
32
How is Ca+ associated with dystophin?
loss of integrity of the membrane causes increased intracellular Ca, which activates proteases that breaks down muscle
33
What are some possible treatments for muscular dystrophy?
1. correction of genetic defect 2. Cell therapy (eg stem cell) 3. pharmacological therapies to prevent symptoms