Integrating Metabolism Flashcards

1
Q

Define “energy coupling”

A

Energy produced by one action or system being used to drive another reaction.

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2
Q

What is an exergonic reaction?

A

A reaction which releases energy (negative ∆G).

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3
Q

What is an endergonic reaction?

A

A reaction which absorbs energy (positive ∆G).

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4
Q

What is anabolism?

A

A reductive reaction.
Energy requiring reaction.
Produce larger complexes from smaller ones.
Uses the energy from catabolism.

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5
Q

What is catabolism?

A

An oxidative reaction.
Energy releasing.
Breakdown of complex molecules to form simpler ones.

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6
Q

What mechanism converts glycogen to glucose-6-phosphate?

A

Glycogenolysis (via glycogen phosphorylase).

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7
Q

Where in the body is glucose-6-phosphate (G6P) primarily used?

A

Muscles:
Important source of energy during high intensity, shorter exercise.
Liver:
G6P converts to glucose and enters bloodstream.

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8
Q

What mechanism converts Glucose-1-phosphate (G1P) to glycogen?

A

Glycogenesis (via glycogen synthase).

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9
Q

Define gluconeogenesis?

A

The synthesis of glucose from non-carbohydrates (i.e. lactate, glycerol, AAs).

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10
Q

Define the Cori cycle.

A

Lactate produced by muscular glycolysis.
Transported to liver.
Converted to glucose.
Returns to muscles for re-use.

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11
Q

What is the term used to describe the sacrifice of muscle protein to produce glucose for the brain?

A

Starvation

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12
Q

Describe what happens during fatty acid oxidation in mitochondria?

A

Short and medium chain fatty acids enter directly.
Long chains shuttle in using carnitine carriers.
Fatty acids broken down to generate Acetyl-CoA molecules.
Beta oxidation occurs.

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13
Q

Describe the beta oxidation of fatty acids?

A

The breaking down of fatty acids to acetyl-coa to either:
Feed into the TCA cycle
OR
Generate ketone bodies.

Each turn generates:
Acetyl-CoA.
A reducing equivalent for electron transport chain.

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14
Q

How is Acetyl-CoA used post-beta oxidation?

A

Acetyl CoA either generates ketone bodies or feeds into tricarboxylic acid cycle.

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15
Q

How is your body supplied with essential and non-essential amino acids?

A

Essential - from diet.
Non-essential - derived from transamination.

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16
Q

What happens in a scenario where there is excess amino acids?

A

The excess are catabolised to urea via deamination.
The deaminated carbon skeletons are oxidised via the tricarboxylic acid cycle.

17
Q

Where does catabolism of amino acids mainly occur?

A

In the liver.

18
Q

What occurs during catabolism of amino acids?

A

Amino group is removed from amino acids (enters urea cycle for excretion).
Carbon skeleton either: Oxidised to CO2 + H20.
Used for gluconeogenesis.
Used for ketogenesis.

19
Q

How is nitrogen metabolised?

A

Amino nitrogen enters urea cycle for excretion.

20
Q

What is the meaning of the term “amphibolic”?

A

A cycle which serves as both catatonic and anabolic.

21
Q

What is anaplerosis?

A

The replenishment of tricarboxylic acid cycle (TCAC) intermediates.

22
Q

What are tricarboxylic acid intermediates? What are their uses?

A

Metabolites which are not used up in the oxidation of acetyl CoA.
Are used in the synthesis of pyrimidines, porphyrins, lipids etc.

23
Q

In anaplerosis, What does pyruvate carboxylase yield?

A

Oxaloacetate.

24
Q

In anaplerosis, what does glutamate dehydrogenase yield?

A

Oxaloacetate.

25
Q

In anaplerosis, what does beta-oxidation of odd-chain fatty acids yield?

A

Succinyl CoA.

26
Q

Briefly describe the meaning of fed -> fasted.

A

Contribution of dietary glucose is replaced firstly at the expense of liver glycogen.
Next is the expense of muscle protein by gluconeogenesis.
Key roles in:
Insulin.
Glucagon.
Cortisol.

27
Q

How does your body deal with carbohydrates in a “fed state” of metabolism?

A

Processes the carbohydrates through:
Glycolysis.
Glycogenesis.
Lipogenesis.

28
Q

How does your body utilise free fatty acids in a “fed state” of metabolism?

A

Triglycerides are synthesised from free fatty acids (FFA).
For storage in adipose tissue

29
Q

How does your body react to a “fed state” of metabolism in terms of amino acids and proteins?

A

Amino acid synthesis occurs.
Protein metabolism occurs.

30
Q

What is the key signal for a “fed” metabolic state?

A

Insulin.

31
Q

In a “fasted state” of metabolism, which mechanisms supply your body with glucose?

A

Glycogenolysis and gluconeogenesis.

32
Q

During a “fasted state” of metabolism, how is adipose tissue utilised?

A

Lipolysis of adipose tissue releases free fatty acids and glycerol.
Glycerol converted to glucose via gluconeogenesis.

33
Q

Why does the body begin oxidating free fatty acids and ketones in the fasted state? How does this affect the body?

A

Oxidation creates a supply of energy, sparing glucose.
Causes ketosis.

34
Q

How does the body utilise proteins and amino acids when in a “fasted state”?

A

Protein catabolism occurs.
Amino acids converted to glucose through gluconeogenesis.

35
Q

How are pancreatic hormones affected by a “fasted state”?

A

Glucagon active.
Insulin suppressed.