Carbohydrates Flashcards

1
Q

What can be metabolised to Acetyl CoA?

A

Alcohol
Fatty acids
Glucose —> pyruvate
Amino acids —> keto-acids

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2
Q

What can be metabolised to urea?

A

Amino acids —> urea

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3
Q

What is the purpose of stage 1 of catabolism?

A

To convert nutrients into a form that can be taken up into cells

Extracellular (GI tract), no energy produced

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4
Q

What happens to the nutrients that have been converted in stage 1?

A

The C-N and C-O bonds are broken and the building block molecules are absorbed from the GI tract into circulation

No energy produced

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5
Q

What is the purpose of stage 2 of catabolism?

A

Degradation of building blocks to a small number of organic precursors (eg. Pyruvate, urea, a-keto acids)

Many pathways- not in all tissues

C-C bonds broken, oxidative, intracellular

Some energy produced as ATP

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6
Q

Describe stage 3 of catabolism

A

Mitochondrial

Tricarboxylic acid cycle (Krebs cycle)

Oxidative, some energy produced as ATP

Acetyl (CH3CO-) converted to 2CO2

Also produces precursors for biosynthesis

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7
Q

Describe stage 4 of catabolism

A

Mitochondrial

Electron transport & ATP synthesis (most energy produced)

O2 required (reduced to H2O)

NADH & FAD2H re-oxidised

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8
Q

What are carbohydrates?

A

Come on dipshit u know what a carbohydrate is

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9
Q

How many units are in a monosaccharide, disaccharide, oligosaccharide and polysaccharide?

A

Mono- 1 duh
Di- 2 cmon now
Oligo- Mkay fairs between 9 and 12 (eg. Dextrins)
Poly- 10-100

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10
Q

What is the glucose concentration in blood?

A

About 5mM

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11
Q

Which cells have an absolute glucose requirement?
What is the value?

A

RBCs, neutrophils, innermost cells of kidney medulla, lens of eye

Approx 40g/24 hours

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12
Q

Which carbohydrases are found attached to the brush border membrane?

A

Lactase
sucrase
pancreatic amylase (1-4 bonds)
isomaltase (1-6 bonds)

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13
Q

Describe primary lactase deficiency

A

Absence of lactase persistence allele
Only occurs in adults
Highest prevalence in north-west Europe

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14
Q

Describe secondary lactase deficiency

A

Caused by injury to the small intestine
eg, gastroenteritis, coeliac disease, Crohn’s disease, ulcerative colitis
Occurs in both infants & adults
Generally reversible

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15
Q

Descibe congenital lactase deficiency

A

Extremely rare
Autosomal recessive defect in lactase gene
Cannot digest breast milk

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16
Q

Describe how monosaccharides are absorbed

A

Active transport into intestinal epithelial cells by SGLT1
Passive transport via GLUT2 into blood supply
Transport via blood to target tissues
Glucose uptake into cells by facilitated diffusion using GLUT1-GLUT5)

17
Q

Describe the features of glycolysis

A

Central pathway of CHO catabolism
Occurs in all tissues (cytosolic)
Exergonic, oxidative, irreversible
Only enzyme that can operate anaerobically (with LDH)

18
Q

Describe the functions of glycolysis

A

Oxidation of glucose
NADH production (2 per glucose)
Synthesis of ATP
Provide biosynthetic precursors for FA, amino acids and nucleotides

19
Q

What does hexokinase (glucokinase in liver) do?

A

Converts glucose to glucose-6-phosphate

20
Q

What does phosphofructokinase 1 do?

A

Catalyses step 3 of glycolysis