what is pharmacokinetics
what the body does to the drug ( ADME)
what is pharmacodynamics
what the drug does to the body
what drug characteristics affect absorption
molecular weight, ionisation, solubility,formulation,liberation
where are pro drugs converted to their active state
liver
main ways of elimination
pulmonary, bile, renal
what is the therapeutic index
min toxic dose/ min effective dose
examples of drugs which are renally cleared
aminoglycosides ( gentamycin), glycopeptides ( vancomucin), digoxin, lithium, morphine
whats chronotropy
effect on heart rate (+ve increases hr, -ve decreases hr)
digoxin effect on heart rate
decreases
what is inotropy
contractility of the heart - increased contractility increases the cardiac output
digoxin effect on contractility
increases contractility
how does digoxin work
inhibits the Na-K ATPase to increase intracellular calcium levels
strengthens heart contractions and slows the heart rate
what kind of drug is digocin
cardiac glycoside
define steady state
same amound eliminated as administered
( a constant serum drug level)
which drugs rapidly reach steady state
drugs which have short half lifes
define potency
amount of drug which reaches 50% efficacy
ED50 vs LD50
effective dose (50% of subject) vs Lethal dose (50% of subjects)
what is responsible for metabolism/elimination of drugs
enzymes
define an agonist
a ligand which binds and activates a receptor
gs protein receptor function
stimulatory
stimulated by adenylyl cyclase , which increases cAMP and activates PKA
Gi g protein function
inhibitory
inhibits adenylyl cyclase which decreases cAMP
Gq g protein function
activates PKC which produces IP3 and DAG which releases intracellular calcium levels and calcium sensitisation
how does mannitol work
interferes osmotically with water reabsorption by kidneys - doesnt interact with the cell
why do receptor mediated responses plateau
theres a finite number of receptors in a cell so once theyre all saturated it plateaus