Post absorption processing of proteins Flashcards

1
Q

what are 5 uses of amino acids

A
proteini synthesis 
synthesis of nitrogen containing metabolites 
energy 
fatty acids/ketone bodies 
glucose/glycogen
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2
Q
what are these amino acids used to turn into (nitrogen containing compounds 
glycine
tyrosine
tyrptophan 
histidine
glycine/arginine
glycine/aspartate/glutamine
A
gly - haem
ty - dopamine, NA, A
trypto - serotonin 
his - histamine
gly/arg - creatine
gly/asp/glut - purine bases
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3
Q

what is kwashiorkor

A

low protein high fibre diet in children of developing countries
poor growth from lack pf proetin and well as immunosuppression as low IG’s
lack of melanin = skin changes
lack of albumin causes lower limb oedema
abdominal bloating from accumulation of fat in the liver and fluid build up

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4
Q

what must happen if amino acids are to be stored as energy

A

the nitrogen must be excreted as can cause tremor, vomiting, cerebral oedema and death

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5
Q

what are the 3 steps of removal of ammonia

A

transamination - transfer of amino group from amino acid to a-ketoglutarate forming glutamate (in most tissues)
deamination - release of ammonia from glutamate (mainly in the liver)
urea synthesis - urea cycle (in the liver)

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6
Q

what molecule must be used to transport ammonia to the liver and describe this process

A

as glutamate or glutamine
amino group from a-KG forms glutamate and another amino group forming glutamine
the reaction is then reversed in the liver to release ammonia

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7
Q

describe the disposal of ammonia

A

step 1 - transfer of amino group from amino acids in a-KG to form glutamate - requires pyridoxal phosphate
step 2 - release of ammonia from glutamate

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8
Q

what is the other name for pyridoxal phosphate

A

Vit B6

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9
Q

what is vitamin B6 used for

A

transamination and synthesis of non-essential amino acids
decarboxylation reactions required for neurotransmitter synthesis
haem synthesis
some aspects of energy metabolism and lipid synthesis

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10
Q

what can lack of vitamins B6 cause

A

anaemia (lack of haem)
neurological symptoms (lack of NT and lipid syn)
poor growth, skin lesions, poor immune reposes (lack of protein syn)

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11
Q

what stimulates the activation of the urea cycle

A

high levels of amino acids

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12
Q

what is the control step in urea synthesis

A

carbamoyl phosphate synthesis

it is allosterically activated by N-acetylglutamate, which is formed when glutamate levels are high

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13
Q

what happens in the mitochondrion and then the cytosol in the urethras cycle

A

mito - carbamoyl phosphate formed from ammonia and bicarbonate (CO2)

carbamyol group transferred to ornithine to form citrulline

in the cytosol – second amino group added from aspartate, arginine formed - urea released

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14
Q

what is the difference between uric acid and urea

A

uric acid is derived from prune nucleotides rather than protein

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15
Q

what is the result of high uric acid in the blood

A

hyperuricaemia leads to deposition of sodium urate crystals in the kidneys (kidney stones) and in the joints (gout)

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16
Q

what is hyperuricaemia due to

A

over production of urate or poor excretion via the kidneys

high purine foods such as beer, red meat and seafood

17
Q

what 3 metabolic pathways use the carbon skeleton of amino acids

A

krebs - makes Atp
fatty acid and ketone synthesis
glucose synthesis - gluconeogenesis

18
Q

which two amino acids can only be ketogenic

A

lysine and leucine

19
Q

when does gluconeogenesis occur

A

during fasting or exercise

20
Q

where does gluconeogenesis usually occur

A

cytosol of the liver and kidney

21
Q

what are the precursors of glugoneogenesis

A
kept acids (derived from amino acids - mainly alanine) 
lactate - from anaerobic glycolysis 
glycerol from triglycerol breakdown
22
Q

how long do glycogen stores last

A

about 18 hours

23
Q

what are the three steps of gluconeogenesis

A

pyruvate - phosphoenolpyruvate
(requires many stages)

fructose 1-6 bisphosphate - fructose 6 phophate
(requires fructose 1,6 bisphosphatase)

glucose 6 phosphate - glucose
(requires glucose 6 phophatase)

24
Q

what causes glycolysis vs gluconeogenesis

A

high glucose and or low energy = glycolysis

low glucose and or high energy = gluconeogenesis

25
Q

what is type 1 diabetes affect on glycolysis and gluconeogenesis

A

no insulin is produced
glycolysis is inhibited therefore blood glucose levels rise

gluconeogenseis is stimulated and blood glucose rise even further

26
Q

why is there rapid weigh loss in type 1 diabetes

A

to provide substrates for gluconeogenesis muscle protein is broken down to provide amino acids

27
Q

what is the cori cycle used for

A

converts lactate from rapidly respiring tissues back to glucose which occur sin the liver

28
Q

how does alcohol make you hungry

A

inhibits gluconeogenesis and lowering blood glucose
high NADH tends to cause conversion of pyruvate and alanine to lactate
this prevents conversion of glycerol to glyceraldehyde 3 phosphate which inhibits gluconeogensis