Topic 3: Energy System Flashcards

1
Q

3.1.1 List the macronutrients and micronutrients

A

Macro:

  • Lipids (Fats)
  • Carbohydrates
  • Protein
  • Water

Micro:

  • Vitamins
  • Minerals
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2
Q

What are macronutrients?

A

Nutrients that provide calories or energy and are required in large amounts

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3
Q

What are micronutrients?

A

Nutrients required in small amounts for various physiological functions but not produced by the body (except vitamin D).

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4
Q

Functions of Carbohydrates

A
  • Fuel
  • Energy storage
  • Cell membrane
  • DNA
  • RNA
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5
Q

Functions of Protein

A
  • Structure
  • Transport
  • Communication
  • Enzymes
  • Protection
  • Fuel
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6
Q

Functions of Lipids

A
  • Fuel
  • Energy storage
  • Cell membrane
  • Hormones
  • Precursor of bile acid
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7
Q

Functions of Water

A
  • Medium for biomechanical reactions
  • Transport of nutrients, metabolites, waste products
  • Thermoregulation
  • Excretion
  • Lubrication of joints and sliding surface
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8
Q

Functions of Vitamins

A
  • Energy release from macro units
  • Metabolism
  • Bone health
  • Blood health
  • Eyesight
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9
Q

Functions of Minerals

A
  • Minerlizations of bones and teeth
  • Blood oxygen transport
  • Defense against free radicals
  • Muscle function
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10
Q

3.1.3. State the chemical composition of a glucose molecule

A

C6H12O6

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11
Q

3.1.4. Identify a diagram representing the basic structure of a glucose molecule.

A
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12
Q

3.1.5. Explain how glucose molecules can combine to form disaccharides and polysaccharides.

A

Condensation Reactions:

The linking of a monosaccharide to another monosaccharide, disaccharide or polysaccharide by the removal of a water molecule.

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13
Q

Monosaccharides

A
  • The most simple form of carbohydrate (sugar)
  • Very easily absorbed by the body
  • Used as metabolic fuel
  • e.g. glucose
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14
Q

Disaccharides

A
  • Combination of 2 monosaccharides
  • Glucose & fructose combination
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15
Q

Polysaccharides

A
  • 10 or more sugar molecules combined
  • e.g. glycogen
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16
Q

3.1.6. State the composition of a
molecule of triacylglycerol

A

1 glycerol molecule + 3 fatty acid chains

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17
Q

3.1.7. Distinguish between saturated and unsaturated fatty acids

A

Saturated Fat - No double bonds between the individual carbon atoms of the fatty acid chain - e.g. meat, poultry, full-fat dairy products, coconut oil, tropical oil

Unsaturated Fat - One or more double bond are formed between carbon atoms - e.g. olive oil, olives, avocado, peanuts, cashew nuts, canola oil

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18
Q

3.1.8. State the chemical composition of a protein molecule

A
  • C, H, O and N
  • Formed by amino acids
  • Linked in chains through peptide bonds
  • The body breaks down food into amino acids and then makes its own protein
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19
Q

3.1.9. Distinguish between an essential and non-essential amino acid

A
  • Essential amino acids cannot be synthesized by the human body and must be obtained from diet
  • Non-essential amino acids can be synthesized by the human body
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20
Q

3.1.10. Describe current recommendations for a healthy balanced diet

A
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21
Q

3.1.11. State the approximate energy content per 100g of carbohydrate, lipid and protein in Kilojoules

A

100g protein = 1720kj

100g carbohydrate = 1760kj

100g fat = 4000kj

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22
Q

3.1.12. Discuss how the recommended energy distribution of the dietary macronutrients differs between endurance athletes and non-athletes

23
Q

Metabolism

A

All the biochemical reactions that occur within an organism, including anabolic and catabolic reactions

24
Q

Anabolism

A

built up molecules and consume energy

25
Q

Catabolism

A

break down molecules and release energy

26
Q

Aerobic Catabolism

A

Compounds breaking down in the presence of oxygen

27
Q

Anaerobic Catabolism

A

Compounds breaking down in the absence of oxygen

28
Q

3.2.2. State what glycogen is and its major storage sites

A
  • When the body has too much glucose for its needs it stores glucose as GLYCOGEN
  • Predominantly in the LIVER and MUSCLE TISSUE
29
Q

3.2.3. State the major sites of triglyceride storage

A

Adipose Tissue and Skeletal Muscle

30
Q

3.2.4. Explain the role of insulin in the formation of glycogen and the accumulation of body fat

A
  • Decrease blood sugar level
  • Tell the body to store excess glucose as glycogen
  • Stimulates lipogenesis (the formation and storage of triglycerides)
  • Excess glucose –> triglycerides –> stored in the adipose tissue as body fat
31
Q

3.2.6. Outline the functions of glucagon and adrenaline during fasting and exercise.

A
  • Increase blood sugar level
  • Exercise or fasting lowers blood glucose –> triggering the pancreas to release glucagon –> stimulates glycogenolysis –> increases blood glucose levels

Adrenaline:

  • Also increases with low glucose levels and also promotes glycogenolysis and lipolysis
32
Q

3.2.7. Explain the role of insulin and muscle contraction on glucose uptake during exercise.

A

Both insulin and muscle contraction stimulate glucose uptake from the blood into skeletal muscle.

33
Q

Glycogenolysis (Catabolism)

A
  • breaking down glycogen into glucose
  • muscle glycogen is used to meet the needs of the muscles ONLY
34
Q

Lipolysis

A

When triglycerides are released into the bloodstream and broken down into fatty acids and glycerol

35
Q

3.3.1 Annotate a diagram of the ultrastructure of a generalized animal cell.

A

Limit to ribosomes, rough endoplasmic reticulum, lysosomes, Golgi apparatus, mitochondrion and nucleus.

36
Q

3.3.2. Annotate a diagram of the ultrastructure of a mitochondrion.

A

Limit to cristae, inner matrix and outer smooth membrane

37
Q

3.3.3. Define the term cell respiration.

A
  • A series of chemical reactions that break down nutrient molecules to produce ATP
  • C6H12O6 + H2O –> 6 CO2 + 6H2O + ATP
38
Q

3.3.4. Explain how adenosine can gain and lose a phosphate molecule.

A

Gain:

  • When a phosphate molecule is added back through energy ADP can be made

Loose:

  • ATP + H2O = ATP - P –> ADP
39
Q

3.3.5. Explain the role of ATP in muscle contraction.

A

The breakdown of ATP to ADP releases a phosphate molecule, which provides energy for muscle contraction

  1. ATP requires synthesizing
  2. PCr is present in muscle cell
  3. PCr is broken down to provide the energy required
  4. 1 PCr molecule produces 1 new ATP molecules
40
Q

3.3.6. Describe the re-synthesis of ATP by the ATP–CP system.

A

PCr is broken down to provide a phosphate molecule for the re-synthesis of ATP that has been utilized during the initial stages of exercise

41
Q

Oxygen debt

A

the extra oxygen needed to restore energy systems after exercise

42
Q

3.3.9. Describe the production of ATP from glucose and fatty acids by the aerobic system.

A
  • With oxygen, pyruvate enters the Krebs cycle, generating electrons for ATP via the electron transport chain.
  • Fats, through beta oxidation, produce more ATP, and proteins are used in extreme cases.
43
Q

3.3.11. Evaluate the relative contributions of the three energy systems during different types of exercise.

A
  • Depending on the sport different energy systems will be used

High intensity:

  • Anaerobic - ATP - PC or Lactic Acid

Moderate:

  • Anaerobic and Aerobic

Low:

  • Aerobic
44
Q

Glycogenesis (anabolism)

A
  • Glucose –> Glycogen
  • When body has too much glucose, it will store the excess glucose as glycogen
  • Glycogen are stored mostly in muscle tissue and liver
45
Q

Lipogenesis

A

The formation and storage of triglycerides into adipose tissue or skeletal muscle

46
Q

Compare and contrast the dietary macronutrient requirements of a trained endurance cyclist and a trained sprint cyclist. [3]

A
  • Endurance cyclist requires a greater proportion of carbohydrates to aid in slow release energy
  • Sprint cyclist requires greater proportion of protein to build muscle required for great power output
  • Both cyclist would have reduced fat intake to increase power to weight ratio
  • Endurance cyclist would require greater quantity of water
47
Q

Explain the phenomena of oxygen deficit

A

Oxygen deficit is when the need of oxygen and oxygen supply do not match in the first moments of exercise

48
Q

Three Energy System

A
  • ATP - PC pathway
  • Lactic Acid pathway
  • Aerobic Pathway
49
Q

Glycolysis (catabolism)

A
  • Anaerobic
  • Occur in cytosol
  • Glycolysis breaks down glucose –> PYRUVATE and ATP (energy)
  • Produces 2 ATP
  • No oxygen –> Pyruvate and ATP
  • Yes oxygen –> Pyruvate to mitochondria
50
Q

Kreb Cycle

A
  • Aerobic
  • Pyruvate to mitochondria
  • Pyruvate –> Acetyl CoA –> enters Kreb Cycle
  • Undergoes reactions –> produce co2 and ATP and high energy electron
  • Produces 2 ATP
51
Q

The Electron Transport Chain

A
  • Occurs in inner membrane of mitochondria
  • Aerobic
  • high energy electrons from kreb cycles –> ETC –> water and ATP
  • Produces 32 - 34 ATP
52
Q

Anaerobic Energy Systems: Creatine Phosphate System (PCr)

A

ATP - PC

  • Anaerobic
  • Duration: 6 - 10 secs
  • Recovery time: 3 mins
  • Used in: High-intensity, explosive sport
53
Q

3.3.7. Describe the production of ATP by the lactic acid system.

Anaerobic Energy Systems: The Lactic Acid System / Anaerobic Glycolytic System

A
  • Anaerobic
  • Glycolysis in cytosol
  • Glycolysis breaks down glucose –> PYRUVATE
  • Pyruvate –> 2 ATP and lactate
  • Duration: up to 2 mins
54
Q

Excess Post Exercise Oxygen Consumption (EPOC)

A

Used for recovery:

  • Remove lactic acid (Lactic Acid system)
  • Restore ATP and PCr (ATP-PC)
  • Restore oxygen level (Aerobic system)