Pharmacogenetics -nanda Flashcards
contrast pharmacogenetics and pharmacodynamics
pharmacogenetics is how the person reacts to the drug, metabilizes it and clears it. pharmacodynamics in downto the molecular level how different drugs interact with their substrates etc.
what is CYP
whre is it found
what does it do?
CYP is a heme containing cytochrome p450.
it is found primarily in the liver where it detoxifies drugs
in addition to detoxifying drugs, what characteristic does CYP2D6 have?
CYP2D6 can also activate drugs. it converts codein to morphine
how can a CYPs play a role in drug interaction?
well there are many CYPs but if you take two drugs that is acted on by the SAME CYP then you will not want to take them together because 1 might not work since the CYP will be busy thus the second drug’s action will be missing
what is Warfrin used to treat?
Warferin is used to prevent thrombosis and embolisms in the heart
what is the direct action of warferin on what molecule?
Waferin succesffully prevents clots by imparing the synthesis of vitamine K dependent clotting factors. Warferin is a competitive inhibitor of vitamin K so it prevents the downstream production of those clotting factors that the body needs vitamin K to make. See picture
why is there such a large variation between tolerance and sensitivity to Warferin?
There are so many CYP pathways that are involved in Wafrin metabolism that a mutation in one can change the tolerance of a person to the drug. see picture
CYP2C9 interaction with Wafrin is considered
pharmacokinetics (drugs in body over time)
how can you describe how there is a continium with the the variability in Warfrin tolerance?
first off there a shit load of CYPs. and Second with every defect in 1 CYP basically takes you down a notch
Gama glutamyl carboxylate of coagulation factors cause clots…how does Warfrin prevent this from happening?
the critical step for this cascade is reducing vitamine K by the Vitamin K epoxide reductase. If Warfrin binds to the VKORC then vitamine K cannot bind to it,vitamine K is never reduced and the clotting factors are never carboxated.
How does altering of the vitamine K reductase play a factor in creating more variation
You can also have a defect in the vitamine K reductase which causes further variation