ATP anaerobic metabolism, glycolysis and high intensity sports Flashcards

1
Q

Phosphocreatine

A

PCr in muscle can be used to reynthesise ATP at very high rates
Limited capacity
PCr restricted to cytoplasm where it is present at a concentration of about 20 mol.kg ww

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2
Q

Glycogenolysis

A

Glycogen breakdown

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3
Q

Glycogenesis

A

Glycogen synthesis

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4
Q

Getting glucose into cells

A

There are 5 different types of glucose transporter
GLUT 4 is stimulated by insulin present in muscle
GLUT 2 is not stimulated: present in liver (which needs to export glucose in fasting when insulin is low)

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5
Q

ATP hydrolysis equation

A

ATP + H20 —-> ADP + P + hydrogen + energy

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6
Q

Phosphocreatine degradation

A

Phosphocreatine breakdown is initiated immediately at the onset of contraction
PCr utilisation is at its highest within 2 seconds of the imitation of contraction
As the rate of PCr breakdown declines, so does the rate of ATP resynthes

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7
Q

The glycolytic pathway

A
  • Starting point is glycogen
  • First reaction involves splitting off the large glycogen molecule of a single glucose molecule which is released as glucose 1 phosphate and this is rapidly converted to glucose 6 phosphate
  • First step catalysed by enzyme glycogen phosphorylase
  • Phosphate group added to the glucose molecule that is added to the glucose molecule from the cell- primes the glucose molecule for subsequent reactions
  • Glucose present in the blood can be taken up by muscle cells and used in glycolysis
  • GLUT 4 transports glucose from the blood to muscle fibres
  • Glucose 6 phosphate then converted to fructose 6 phosphate
  • Net gain from anaerobic glycolysis is 2 ATP molecules starting from glucose
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8
Q

Phosphofruktokinase

A

An important enzyme in all living cells

Performs the committed step in the glycolytic pathway- conversion of fructose 6 phosphate

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9
Q

Acids and bases

A

Using ATP produced hydrogen

Lactic acid causes drop in PH

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10
Q

Why is acidity in the muscles an issue

A

Affects calcium transport, rate of glycolysis, fatigue

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11
Q

Bicarbonate buffering

A

Achieved by the infection of a dose of about 0.3g NaHCO3 per kg body mass
Can neutralise some of the excess acidity in muscles
Allows hydrogen to leave muscles faster
This allows more hydrogen and lactate to be produced before muscle acidity reaches limiting levels

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12
Q

Oxidation of carbohydrates

A

Carbohydrate converted to pyruvate by glycolysis
Pyruvic enters mitochondria and TCA cycle
Entry of pyruvate molecules into the mitochondria
Further metabolism of pyruvate catalysed by the enzyme pyruvate dehydrogenase
To prime the pyruvate molecule for subsequent reactions, it is attached to a molecule of co Enzyme A and at the same time one of the carbon atoms is lost as carbon dioxide, yielding acetyl co a

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13
Q

Oxidation of amino acids

A

Some amino acids can be oxidised
Amino group must be removed by transferring it to another molecule called a keto acid resulting in the formation of a different amino acid
this process is called transamination
Or amino group can be removed to form free ammonia
Keto acid eventually oxidised to cos and h20 in TCA

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14
Q

Oxidation of fat

A

Free fatty acids from adipose tissue, some intramuscular fat
Fat has to be used to be oxidised to be used
2 carbon units sequentially removed by free fatty acids via beta oxidisation to generate acetyl co A
acetyl co A

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15
Q

Lipolysis

A

The breakdown of triglyceride into its fatty acid and glycerol components

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16
Q

Beta oxidisation

A

Fatty acids broken down to acetyl co A in the mitochondria

17
Q

Control of Krebs

A

Glycolysis connects with Krebs
2 enzymes achieve opposite aims in conflict
If you can increase rate of enzymes, balance the pyruvate the dehydrogenase
Pyruvate dehydrogenase has 2 forms- one active and one inactive
Active- glycolysis connects with krebs
more calcium concentration outside the sarcoplasmic reticulum activates pyruvate dehydrogenase
Increased concentration of pyruvate indicating glycolysis has sped up, pyruvate switches off the enzyme which switches off pyruvate dehydrogenase