Session 2 Flashcards

(23 cards)

1
Q

what are the 4 stages of carbohydrate metabolism?

A

stage 1
- breakdown of building block moeclules for absorption

  • occurs in the GI tract (extracellular)

stage 2
- breakdown to metabolic intermediates
- oxidative: releases reducing power (NADPH)
- in cytoplasm

stage 3
- TCA/Krebs cycle
- oxidative: released reducing power
- in mitochndria

stage 4
- oxidative phosphorylation
- ATP
- in mitochondria

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2
Q

what are carbohydrates?

A

general formula: (CH20)n

if they have aldehyde group: aldose

if they have ketone group: ketose

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3
Q

what are the 3 main dietary monosaccharides?

A
  • glucose, fructose, galactose

— they are structurally similar and only differ in some chiral carbons

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4
Q

which cells have an absolute requirement of glucose?

A
  1. RBC
  2. Neutrophils
  3. innermost cells of kidney medulla
  4. CNS
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5
Q

why do RBC and lens fiber cells only metabolise glucose?

A

they have no mitochondria: cannot undergo oxidative phosphorylation

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6
Q

why can neutrophils only use glucose?

A

they’re in an environment where ox phosphorylation cannot happen

  • or their mitochondria is being used for something else
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7
Q

how’s much glucose does the CNS use?

A

140g/24 hours

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8
Q

why can’t humans digest cellulose?

A

no enzymes are produced to breakdown the beta 1-4 linkages

enzyme = glycosidase that recognises beta structure

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9
Q

what is the difference between alpha and beta glucose?

A

alpha = more flexible, can be forced and stored compactly

beta = more linear and rigid for structure

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10
Q

what is lactose?

A

a disaccharide broken down by lactase in stage 1 of glycolysis

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11
Q

what is the normal phenotype of lactase?

A
  1. during gestation and in newborn babies the levels of lactase are high
  2. by age 5-7 lactase levels drop to 10% of the original
  3. normal phenotype = lactose deficiency as adult
  4. some populations have lactose persistence in adulthood whom can consume lactate products —> not normal
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12
Q

what is lactose intolerance?

A

lactase deficiency

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13
Q

what are the 3 types of lactose intolerance?

A
  1. primary lactase deficiency
  2. secondary lactase deficiency
  3. congenital lactase deficiency
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14
Q

what is primary lactose?

A

adult lactase deficiency (cannot digest lactose)

  • they don’t have lactose persistence allele
  • age related: declines
  • only in adults
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15
Q

what are the symptoms of lactose intolerance?

A
  • bloating
  • flatulence
  • diarrhoea
  • vomiting

—> build up of undigested lactose is metabolised by bacteria in colon which releases CO2 and methane
- leads to dehydration as water drawn into tissues

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16
Q

what is secondary lactase deficiency?

A

caused by injury to small intestine —> inflammation to small intestine

  • lactase levels drops
  • reversible
  • e.g gastroenteritis
17
Q

what is congenital lactase deficiency?

A

autosomal recessive defect in lactase gene

  • extremely rare
18
Q

what is the treatment of lactose intolerance?

A

remove lactose from diet

19
Q

how is glucose and galactose absorbed?

A

actively transports into the intestinal epithelial cells by SGLT1

  • depends on sodium potassium pump
  • then passively diffuses from epithelial cells to blood via GLUT -2
20
Q

how is fructose absorbed?

A

passively transported into epithelial cells via GLUT -5

  • then passively transported into the blood via GLUT -2
21
Q

how do target tissues receive glucose, fructose and galactose?

A

facilitated diffusion using transport proteins (GLUT -1 to GLUT -5)

  • different tissues have different glucose transports
22
Q

what are the symptoms of hyper and hypoglycaemia?

A

hyperglycaemia
- caused by diabetes
- nerve and blood vessel damage due to inflammation

hypoglycaemia
- fainting
- seizures
- cognitive impairments
—> due to brain not getting glucose

23
Q

what is stage 1 of carbohydrate metabolism?

A

enzymes such as amylase break down starch into maltose in the saliva

  • disaccharidases attached to border membrane of epithelial cells secreted to hydrolyse maltose into glucose