FINAL Flashcards
AVD=
dose/[] in blood
Met. phases?
I = Inactivate drugs (P450), but still lipid soluble II = Conjugation ->Now water soluble
Enzyme induction=?
Drug A->more enz.->less of drug B
codeine, B-blockers and tryciclic metabolized by?
2D6
Kidney urine Excretion=
filtration + secretion -reabsorption
Drug clearance=?
Qt of drug eliminated in given time
First vs zero order kinetics?
First = Constant fraction, normal Zero = Constant amount
Ligand gated ion channel Eg?
Nicotinic, GABA, glutamate, serotonin
GCPR Eg?
Opiods, muscarinic
GCPR activation occurs when?
GDP->GTP and dissociation of alpha subunits
Kd?
Affinity constant, Concentration of drug that bind to half the receptors. Low Kd = high affinity
Potency vs efficacy?
amount for effect
Max effect produced
Caffeine CYP?
1A2
Kinetics difference with elders?
Decrease: renal clearance, increase fat, decrease phase 1 metabolism, decrease first-pass
Kinetics vs dynamics tolerance?
K=Drug broken down more rapidly. Dose response curve (DRC) the same for same blood concentration of the drug.
D=Decreased effect when reaches receptors. DRC to the right at same drug concentration
Withdrawal effect are?
The opposite of drug effect
Tolerance is the idea of?
having to give more of the drug to have same effect