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61 Cards in this Set
- Front
- Back
Unlike glucose and fatty acids, amino acids
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can not be stored
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amino acids can be broken down and used as
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fuel and carbons for glucose/lipid synthesis
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N component of amino acids
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can not be used= build up of ammonia
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Why is ammonia toxic?
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Increases pH alters the redox balance, can disrupt protein strucutre/function
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Ammonia can disrupt
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ox-phos protin gradient
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Degraded ammonia is secreted in the urine as
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urea
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Positive N balance
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N input> output (childhood, pregnancy)
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Negative N balance
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Ninput < N output (dietary deficiency, disease)
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Muscule protein broken down for crucial functinos
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gluconeogenesis and synthesis or protein in other tissues
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Hypercatabolic state
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increased fuel storage, body needs energy and precursors for defense, mobilize fat for energy, negative N balance,
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Amino acids come from
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dietary protein, endogenous protein turnover, Endogenous AA synthesis
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10 essential proteins from diet
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F, V, W, T, I, M, H, R, K, L
Phenylalanine, Valine, Tryptophan, Threonine, Isoleucine, Methionine Histidine, Arginine, Lysine, Leucine |
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Arginine
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essential for growth and only made in urea cycle
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Alanine, aspartate and glutamate are made through
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transamination of pyruvate, oxaloacetate and a-ketoglutarate respectively
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Tyrosine is made from
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phenyalynine
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Urea cycle is the highest when
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you've just eaten and breaking down proteins, or when fasted and need muscle proteins/amino acids for gluconeogensis
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acid in stomach helps
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denature proteins so easily cleaved
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You ate proteins what happens to the amino acids
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some will be used to make proteins, others brea kdown to make energy or stored as fat
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Fasting-protein
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muscle protein break down into amino acids for gluconeogensis, some break down for energy and some to make proteins
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Urea cycle is at its highest when
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amino acids are being broken down, just eaten protein or fasting and amino acids used for gluconeogenesis
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Amino acids unneeded for protein synthesis must
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remove the amino group to be broken down
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amino acids catbolized by
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transamination or deamination
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amino acid gives amine group to
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alpha-ketoglutarate producing glutamate
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Pyruvate to alanine uses
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ALT
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Aspartate to OAA uses
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AST
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Aminotransferases required
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pyridoxal phosphate
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PLP made in liver from
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vitamin B6 and trasnfers a Nitrogen gruop in aminotransferases reactions
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Glucogenic carbons
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degrade to pyruvate or TCA cycle intermediates
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Ketogenic carbons
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ultimately degraded to acetyl CoA acetoacetate
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Insulin promotes
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AA uptake and protein synthesis
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Glucagon and cortisol stimulate
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amino acid uptake in liver
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Glucocorticoids induce
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ubiquitin synthesis, cortisol simtulates gluconeogensis so AAs needed to provide precursors
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Brain needs AA to make
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neurotransmitters
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Liver uses a lot of _____ in the fasted state
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amino acids
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muscle is a major source of ____ in fasted state
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amino acids
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muscle protein has a lot of
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branches chain amino acids
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many tissues can also use ____ in a fast
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glutamine
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Glutamate can be deaminated by
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glutamat dehydrogenase
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What is produces in glutamat deamination?
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ammona and alpha-ketoglutarate
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Where does glutamate deamination occur
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in liver and kidney an dmuscle if need to regenerate alpha-ketoglutarate
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Deamination of glutamate releases____
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nitrogen and goes to urea cycle
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3 other ways free ammonia is made
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purine metabolism, bacterial metabolism in gut, and metabolism of serine and threonine
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glutamate can also carry free____
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ammonia
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Ammonia can also be transferred as
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Alanine
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In liver alanine gives ammino grup back to glutamat regenerating
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pyruvate
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3 molecules that can carry ammonia
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glutamate, glutamine, and alanine
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urea is transported
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from the blood to kidneys for excretion
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Where does aspartate for urea cycle come from?
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glutamine break down in liver by glutaminase
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Synthesis of urea is
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irreversible
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first two step of urea take place in
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mitochondria
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CPS1 is
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rate limiting step
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Second N comes from
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aspartate
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Arginine is made from
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urea cycle
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Urea cycle uses
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ATP
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BUN go up if
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kidney failure or high protein diet
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BUN decrease w
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liver failure
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urea impairment results in
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hyperammonia
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Hereditary urea cycle disorders linked to
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autosomal recessive except for ornithine transcarbomylase is X linked
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CPS1 is stimulated by
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NAG made by acetyl coA and glutamate
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cortisol
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cortisol is primary hypercatabolic breakdown for protein it stimulates ubiquitin synthesis
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Insulin activates
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PFK2, acetyl coA carboxylase, glycogen synthase, and pyruvate kinase
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