Energy Production: Carbs 1+2 Flashcards

1
Q

What occurs in stage 1 of metabolism?

A

Occurs extracellularly (GI tract), complex molecules are broken down to smaller molecules. Breakage of C-N and C-O bonds, and no energy is produced.

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2
Q

What occurs in stage 2 of metabolism?

A

Occurs intracellularly (cystolic and mitochondrial). Has many pathways, C-C bonds are broken and some energy is produced.

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3
Q

What occurs in stage 3 of metabolism

A

Occurs in mitochondria, a single pathway (TCA cycle), is oxidative and some energy is produced. Acetyl CoA is converted to 2CO2.

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4
Q

What occurs in stage 4 of metabolism?

A

Occurs in mitochondria. Electron transport and ATP synthesis. NADH and FAD2H re-oxidised and large amounts of energy carrier (ATP) generated.

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5
Q

What’s the general formula for carbohydrates?

A

(CH2O)n, may contain aldehyde (H-C=O) or keto (-C=O) group

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6
Q

Examples of dietary carbohydrates?

A

Sucrose (Glucose-Fructose disaccharide), Lactose (Glucose-Galactose disaccharide), Maltose (Glucose-glucose disaccharide)

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7
Q

Which tissues have an absolute requirement for glucose?

A

Red blood cells, neutrophils, innermost cells of kidney medulla, lens of eye

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8
Q

Describe primary lactase deficiency

A

Inability to digest lactose products due to an absence of lactase persistence allele. Only occurs in adults.

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9
Q

What causes secondary lactase deficiency?

A

Caused by injury to small intestine, e.g. gastroenteritis, coeliac disease, Crohn’s disease. Occurs in both infants/adults and is generally reversible.

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10
Q

Describe congenital lactase deficiency

A

An autosomal recessive defect in the lactase gene, meaning breast milk can’t be digested.

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11
Q

What does allosteric mean?

A

An activator or inhibitor that binds at ‘another’ site.

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12
Q

What are key features of glycolysis?

A

Oxidation of glucose, NADH production (2 per glucose), synthesis of ATP from ADP with a net gain of 2 ATP.

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13
Q

What are the allosteric and hormonal regulators of phosphofructokinase?

A

Allosteric: inhibited by high ATP and high citrate, stimulated by high AMP and high F2, 6BP. Hormonal: Stimulated by insulin, inhibited by glucagon.

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14
Q

When is pyruvate reduced to lactate?

A

When there is an inability to use NADH for oxidative phosphorylation

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15
Q

What’s the equation for lactate production

A

NADH + H+ + pyruvate <—> NAD+ + lactate
(Lactate dehydrogenase)

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16
Q

What is lactic acidosis

A

Occurs when plasma lactate concentration is above 5mM, above renal threshold and blood pH is lowered.

17
Q

Diseases associated with fructose metabolism.

A

Essential fructosuria- where fructokinase is missing (fructose in urine). Fructose intolerance- aldolase missing so F1P accumulates in liver causing damage and possible death. Managed by removing fructose and sucrose from diet.

18
Q

What enzymes are involved in galactose metabolism

A

Galactokinase, Galactose-1-P uridyl transferase, UDP-galactose 4’-epimerase.

19
Q

Describe galactosaemia

A

Body unable to utilise galactose due to enzyme deficiencies. Problem here is that galactose enters other pathways. Accumulation of galactose-1-P affects liver, kidney and brain. Treatment- no lactose in diet.