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What are the three processes involved in renal excretion
Glomerular filtration
Tubular reabsorption
Tubular secretion
what is glomerular filtration
a process where xenobiotics are filtered from the blood into the kidney tubule
What is tubular reabsorption
A xenobiotic moves from the kidney tubule back into the blood → reducing its elimination
What is tubular secretion
a xenobiotic is actively/facilitated transported from the blood into the kidney
What is biliary excretion
excretion of xenobiotics or metabolites from the liver into bile, which carries them into the intestine
what is enterohepatic cycling
xenobiotics or metabolites excreted into the intestine through bile can be reabsorbed and returned to the liver
what effect can enterohepatic cycling have on a xenobiotic
It can increase the xenobiotic’s half-life by allowing it to be reabsorbed instead of eliminated
why can enterohepatic cycling increase toxicity
if a xenobiotic produces toxic metabolites, repeated reabsorption can increase exposure and exacerbate liver toxicity
how is ethanol related to pulmonary excretion
about 90% of ethanol is metabolized in the liver, while approx. 2% is excreted in expired air
Why can breathalyzers detect alcohol
Because some ethanol is excreted in expired air, allowing alcohol to be detected in breath
How can lactation eliminate xenobiotics
Lipophilic xenobiotics can be excreted into breast milk
what are the four important types of xenobiotic interactions
summation
synergism
potentiation
antagonism
what is summation
the combined effect equals the sum of the individual effects (2+2=4)
What is synergism
the combined effect is greater than the sum of the individual effects (2+2 = 10)
what is potentiation
one xenobiotic has no effect by itself but increases the effect of another (2+0=10)
what is antagonism
the combined effect is less than additive (2+2=1)
at what four stages can xenobiotic interactions occur
biotransformation
distribution
excretion
absorption
how can xenobiotics interact during biotransformation
by causing induction or inhibition of Phase I or Phase II enzymes
How can xenobiotics interact during distribution
They can compete for plasma or cellular protein-binding sites
what can happen when a xenobiotic is displaced from a binding protein
the free/unbound fraction increases → producing a greater response
how can xenobiotics interact during excretion
one xenobiotic can inhibit renal excretion of another → decreasing clearance
how can xenobiotics interact during absorption
substances that change GI and pH can alter xenobiotic absorption