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61 Cards in this Set

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