SKELETAL MUSCLE: METABOLISM Flashcards

1
Q

Describe the overall process of energy usage and the available sources of fuel used during exercise

A
  • See flowchart from lecture
  • Sources of fuel: Diet - food entering blood in absorption phase (2-3 hrs after a meal); release of stored fuel during postabsorptive stage(especially during sleep or during a fast or prolonged exercise)
  • Fuel is ingested and broken down to glucose, free fatty acids, amino acids, and ketone bodies. Fuels are oxidized. 60% is converted to heat and 40% isconverted into ATP. Note that ATP is at a constant universal amount and not stored. ATP is used for energy for structural integrity, differentiated function, growth and division, and in response to stimuli and stress.
  • Result: 60-70% used for resting metabolic rate; 25-30% used for movement
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2
Q

Describe the different energy sources during exercise and their general timeline

A
  • ATP + creatine phosphate (0-2 minutes)
  • Anaerobic glycolysis (0-5 minutes): muscle glycogen
  • Aerobic oxidation (3 minutes - 4+ hours): plasmic free fatty acids and adipose tissue triglycerides
  • Aerobic oxidation (3 minutes - 4+ hours): muscle glycogen, plasma glucose, liver glyxogen
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3
Q

Skeletal muscle fibres have enough stored ATP for about ___ of contraction

A

3 seconds

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4
Q

Why is skeletal muscle fibre energy storage not very effective?

A

not very energy dense, is an ineffective energy store for longer duration exercise

  • remember, only stores enough ATP for 3s of contraction
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5
Q

What is the role of creatine phosphate (PCr) in muscle fibres?

A

can be quickly broken down to make more ATP

Can supply energy needs of contraction for ~10s but is regenerated

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6
Q

How does the liver play a role in blood glucose regulation?

A
  • Liver glucose contributes to blood glucose levels when needed
  • Gycogen synthases adds glucose to glycogen. The liver stores ~100g of glycogen
  • Glycogen phosphorylase removes glucose molecules from glycogen.

The liver expresses Glucose-6-phosphatase. Thus, glucose from the liver glycogen can directly contribute to blood glucose levels.

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7
Q

What is the role of muscle glycogen?

A

It is mobilized (converted to glucose) for energy use during exercise. Muscle glycogen can be broken down into glucose monomers via glycogenolysis. Requires glycogen phosphorylase

  • muscle can store ~400g of glycogen.
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8
Q

Describe glycolysis

A

Glycolysis is an important metabolic pathway

  • ~12 chemical reactions occur. Note this is not as quick as creatine phosphate is in ATP generation
  • Provides enough energy for ~90s of contraction
  • Anaerobic (does not require O2)
  • Lactic acidic is a by-product which causes fatigue and potentially muscle soreness?
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8
Q

Describe aerobic respiration

A
  • slowest route to regenerate ATP
  • supply ATP for several hours (if fuel lasts)
    occurs in mitochondria
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9
Q

Q: Why are there differences in oxidative and glycolytic metabolism capaicties across muscle fibre types?

A

Different MHC isoforms lead to differences in ATPase activity and kinetics

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10
Q

Describe the difference across muscle fibres in terms of
- oxidative capacity, mitochondrial content, capillary density, myoglobin
- glycolytic capacity

A

Type I slow twitch muscle fibers:
- High oxidative capacity, mitochondrial content, capillary density, myoglobin
- Moderate glycolytic capacity

Type IIb
- Low oxidative capacity, mitochondrial content, capillary density, myoglobin
- High glycolytic capacity

Type IIa
- Very high oxidative capacity, mitochondrial content, capillary density, myoglobin
- High glycolytic capacity

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11
Q

Describe the process of generating ATP from free fatty acids

A
  • Free fatty acids released from adipose tissue by lipolysis circulate in blood bound to albumin
  • Free fatty acids transport proteins move free fatty acids into muscle cells
  • Free fatty acids bypass glycolysis and enter the Kreb’s cycle through conversion to various intermediates (e.g. acetyl CoA)
  • Free fatty acids require carnitine palmityltransferases (CPTs) to cross the mitochondrial membrane
  • Each cycle of Beta-oxidation removes two carbons and generates one acetyl CoA
  • Free fatty acids products participate in oxidative phosphorylation (Kreb’s, ETC)
  • Also produces FADH2 (1) and NADH (1)
  • Yields up to 17 molecules of ATP making it a more efficient source of energy compared to carbohydrates/amino acids
    9kcal/g (lipids) vs 4kcal/gram (carbs/protein)
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12
Q

Describe the process of generating ATP from amino acids

A
  • Amino acids are the last resort as a source of fuel. The body will maintain proteins as long as possible
  • Amino acids can be oxidized after transamination (transfer of amino group to another molecule)
    • The amino group must be removed because it can give rise to ammonia, which is highly toxic
  • Bypasses glycolysis: carbon skeletons of amino acids enter Kreb’s cycle via conversion to various intermediates (e.g. pyruvate, acetyl CoA)
  • The use of amino acids for energy is coupled to the urea cycle in the liver (converts ammonia to urea, we won’t discuss the details here)
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13
Q

Describe energy sources at rest

A
  • Circulating fatty acids are primary energy source
  • O2 is abundant, and aerobic metabolism is used
  • Glucose taken in is stored as glycogen
  • Phosphocreatine reserves are built up
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14
Q

Describe energy sources at intense activity

A
  • Engaged in your favorite high-intensity sport
  • Muscles lack O2 to support mitochondria
  • Muscles rely on glycolysis for ATP
  • Pyruvic acid build up, is converted to lactic acid
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14
Q

Describe energy sources at moderate activity

A
  • Phosphocreatine reserves are used first, but quickly used up
  • Muscles use aerobic metabolism of fatty acids and glucose released from glycogen stores to make more ATP
15
Q

List 4 facts of mitochondrial DNA gone over in lecture.

A
  • Mitochondria has their own DNA which is separate from nuclear DNA
  • Mitochondrial DNA is not protected like nuclear DNA meaning it is more prone to mutation.
  • Mitochondrial diseases are often exercise-related, and associated with lactic acidosis
  • Mitochondrial DNA is used to identify evolutionary relationships
16
Q

Describe symptoms in the skeletal muscle if they have a mitochondrial disease

A
  • weakness
  • fatigue
  • exercise intolerance
  • Myopathy: muscle disease - weakness in muscle
  • Hypotonia: decreased muscle tone
17
Q

Describe method 1: embryo repair for mitochondrial donation

A
  • Nucleus from parent’s embryo and donor embryo is removed
  • The parent’s nucleus is inserted into the donor’s embryo

This is what happens when the parents embryo has unhealthy mitochondria. They find a donor with healthy mitochondria

18
Q

Describe method 2: egg repair for mitochondrial donation

A
  • Nucleus from mother’s egg and donor egg is removed
  • The mother’s nucleus is inserted into the donor’s egg

This is what happens when the parents embryo has unhealthy mitochondria. They find a donor with healthy mitochondria