Pharmacodynamics Flashcards
Describe the basic drug-receptor theory
Agonist drug binds to receptor = Activation = Response
Measure response via organ bath simulation at contraction/relaxation of tissue
Define affinity (KD)
Tendency for ligand to form stable complex with receptor
Governed by bonds and shape of ligand
Define an agonist and its two components
A drug that binds to receptors to produce a response
- Binds to occupy a receptor (Affinity)
- Produces a response (efficacy)
Define Bmax
Maximum number of binding sites, Measures saturation
Define Dissociated constant, Kd (M)
Affinity of binding (how well drug binds to receptor)
Is a higher or lower Kd better and why?
Lower Kd = Means it has highest affinity to fully bind at lowest conc
Define an antagonist
The drug that binds to a receptor without mediating a response but blocks agonist response
What are the 5 types of antagonism?
Competitive antagonism (reversible/irreversible) receptor effector block (non-comp), chemical, pharmacokinetic, physiological antagonism
Describe non competitive antagonism
Blocks receptor activation and response, doesn’t compete for receptor site
Describe chemical antagonism and an example
2 substances combine in solution, effect of active drug is lost
Eg chelating agents that bind to heavy metals reduce toxicity