Muscle wasting and myostatin Flashcards

1
Q

What is the relation of grip strength with forearm diameter?

A

highly correlated

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2
Q

What does muscle growth rely on?

A
  • mechanical stimulus (exercise)
  • endocrine factors (testosterone, insulin, IGF-1, myostatin, follistatin)
  • essential amino acids
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3
Q

Specifically, how would the signalling and activation of satellite cells work like?

A
  1. Cytokines, growth factors, integrin signalling - they bind to surface receptors to produce transcription factors.
  2. The transcription factors and external androgens and glucocorticoids affect the nucleus. Affects IGF-1/MGF, myostatin, mRNA, rRNA.
  3. Translation initiation of ribosomal, regulatory and myofibrillar proteins take place. Due to factors like the mTOR, activated by the external IGF-1/MGF and insulin, binding to surface receptors
  4. Satellite cells are activated by the binding of IGF-1/MGF, myostatin and growth factors binding to surface receptors
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4
Q

What can cause muscle atrophy?

A
  1. Myostatin binds to ARIIB receptor on sruface
  2. This activates precursor activity involving the I-Smad, co-Smad and R-Smad
  3. MyoD/myogenin is inhibited and this reduces differentiation and cause atrophy
  4. Myostatin binding inhibits AKT pathway, hence inhibiting FoxO1.. this eventually increases degradation and cause atrophy
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5
Q

What can cause muscle hypertrophy?

A
  1. IGF-1 binds to surface receptor
  2. Activates AKT which activates mTOR
  3. Eventually increasing synthesis
  4. Causing muscle hypertrophy
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6
Q

What can be said of satellite cells and hypertrophy?

A
  • Muscle fibres are permanently differentiated so they cannot add new nuceli in times of hypertrophy
  • myonuclear number increases during hypertrophy to maintain myonuclear domain
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7
Q

Can muscle memory last into older age? What type of stimuli could lead to this?

A

Yes. Anabolic stimuli

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8
Q

What 4 factors describe ageing?

A
  1. Universal (all species)
  2. Intrinsic (causes are endogenous)
  3. Progressive (the changes occurring)
  4. Deleterious (phenomenon associated are ‘bad’)
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9
Q

What are the 2 theories for reasons we age?

A
  • programmed theory

- damage/error theory

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10
Q

What is included in programmed theory?

A
  • programmed longitivity
  • endocrine theory
  • immunological
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11
Q

What is included in the damage/errors theory?

A
  • wear and tear
  • rate of living
  • cross-linking
  • free radicals
  • DNA damage
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12
Q

TRUE OR FALSE. Ageing is not homogenous.

A

TRUE

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13
Q

What is the endocrine hypothesis investigated in mice?

A
  • impairs hypertrophy and recovery from injury in vitro

- cause an ageing phenotype in younger mice

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14
Q

Does resistance exercise increase basal testosterone in older males?

A

No

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15
Q

Can we use complex interactions of endocrine factors to predict function with ageing?

A

Yes (but one marker may not be enough)

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