PHYSIOLOGY - Aerobic and Anaerobic Metabolism Flashcards

1
Q

What is the structure of mitochondrial DNA?

A

Circular double stranded DNA

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2
Q

How many proteins are encoded by mitochondrial DNA?

A

37 proteins

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3
Q

(T/F) Mitochondrial DNA are inherited from the paternal lineage

A

FALSE. Mitochondrial DNA are inherited from the maternal lineage

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4
Q

What facilities particle transport across the mitochondrial membrane?

A

The outer mitochondrial membrane has porin proteins which allow for passive transport and translocator outer membrane (TOM) complexes which allow for active transport. Furthermore, the inner mitochondrial membrane has translocator inner membrane (TIM) complexes which also allow for active transport

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5
Q

What is reflected by the number of mitochondria in a cell?

A

The number of mitochondria in a cell reflects the metabolic demand of the tissue

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6
Q

How are mitochondria highly dynamic organelles?

A

Mitochondria can undergo cellular migration, fusion, fission and turnover depending on the metabolic demands of the cell

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7
Q

What is the primary function of the mitochondria?

A

Production of ATP

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8
Q

What is the net production of ATP per unit of glucose?

A

38 ATP per unit of glucose

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9
Q

Where does glycolysis occur?

A

Cytosol

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10
Q

Where does the citric acid cycle occur?

A

Mitochondria

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11
Q

Briefly describe the process of glycolysis and the citric acid cycle

A

Glycolysis is the breakdown of glucose into pyruvate. Pyruvate is then converted into acetyl CoA which enters the citric acid cycle which produces both ATP and high energy electron donors (NADH and FADH2)

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12
Q

Where does the electron transport chain occur?

A

Mitochondria

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13
Q

Briefly describe the electron transport chain

A

Electrons from NADH and FADH2 enter the electron transport chain and are passed along the protein complexes. As the electrons move along, protons are pumped across the inner mitochondrial membrane, creating a proton gradient which stores potential energy. When the protons flow back through ATP synthase, the stored energy is released to drive the production of ATP

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14
Q

What is the main benefit of anaerobic respiration?

A

Anaerobic respiration allows for quicker ATP production without the need for oxygen which is beneficial for short-duration intense exercise

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15
Q

What are the three disadvantages of anaerobic respiration?

A

Lactic acid accumulation
Less efficient ATP production compared to aerobic respiration
Oxygen dept

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16
Q

What is oxygen dept?

A

Following anaerobic respiration, the body must replenish the oxygen levels to break down the lactic acid that has accumulated in the blood and to restore normal metabolic function

17
Q

What causes type A lactic acidosis?

A

Lactic acidosis caused by tissue hypoperfusion

18
Q

List three possible causes of type A lactic acidosis

A

Hypovolaemia
Cardiac failure
Sepsis

19
Q

What causes type B lactic acidosis?

A

Lactic acidosis caused by cellular dysfunction and localised tissue hypoperfusion

20
Q

List three possible causes of type B lactic acidosis

A

Mitochondrial disease
Excessive exercise
High grain diet in ruminants

21
Q

Describe the process of non-shivering thermogenesis

A

Uncoupling protein 1 (UPC 1) found in the inner mitochondrial membrane of brown adipose tissue is activated and forms a preferential pathway for protons to cross the inner mitochondrial membrane and generate heat

22
Q

Why are pigs at such high risk of neonatal hypothermia?

A

Pigs lack a functional uncoupling protein 1 (UPC1) for non-shivering thermogenesis

23
Q

Which method is used by piglets for thermogenesis?

A

Uncoupling protein 3 (UPC 3) in skeletal muscle for muscle based thermogenesis

24
Q

What causes malignant hyperthermia is pigs?

A

Inherited Ryanodine mutation

25
Q

(T/F) Mitochondrial function increases with ageing

A

FALSE. Mitochondrial function decreases with ageing

26
Q

What is the role of reactive oxygen species in ageing?

A

Reactive oxygen species can cause damage to lipids, proteins and nucleic acids - these damages can accumulate and contribute to ageing

27
Q

What is fanconi syndrome?

A

Dysfunction of the proximal convoluted tubule causing malabsorption of electrolytes and nutrients

28
Q

What is the cause of fanconi syndrome?

A

Mutation in the gene encoding for enoyl-CoA

29
Q

What are the five clinical signs of fanconi syndrome?

A

Stunted growth
Diarrhoea
Hypokalaemia
Hyponatraemia
Hypochloraemia

30
Q

What is maple syrup urine disease?

A

Inherited aminoacidopathy (dysfunctional amino acid metabolism)

31
Q

What is the cause of maple syrup urine disease?

A

Dysfunction in the branch chain keto acid dehydrogenase (BCKDH) enzyme which breaks down branch-chain amino acids leading to an accumulation of leucine, valine and isoleucine

32
Q

What is the most distinctive clinical sign of maple syrup urine disease?

A

Urine has a sweet odour