M&R Drugs and receptors Flashcards
What is the difference between:
Drug affinity
Drug efficacy
Drug potency
Drug affinity is the strength that the drug binds to the receptor
Drug efficacy is the ability of the drug-receptor complex to produce maximum functional response (must be a measurable response)
Drug potency takes into account both affinity and intrinsic efficacy (ability to activate receptor). EC50 or effective concentration giving 50% of the maximal response is a measure of potency
Define:
agonist
partial agonist
antagonist
An agonist activates the receptor (has affinity and efficacy)
A partial agonist produces a less than maximal response even with full receptor occupancy, due to lower intrinsic activity
An antagonist blocks the binding of an endogenous agonist (has affinity only)
What are the benefits of using a partial agonist?
Can allow a more controlled response
Can act as an antagonist if there are high levels of full agonist
e.g. methadone for the management of opioid dependence (e.g. heroin)
What are the 3 ways in which an antagonist can act?
- Reversible competitive antagonism
Most common and important in therapeutics
Relies of dynamic equilibrium between ligands and receptors
Can be overcome by high [agonist]
Higher conc = greater inhibition - Irreversible competitive antagonism
Occurs when antagonist dissociates slowly or not at all
Cannot be overcome by increasing [agonist] - Non-competitive antagonism
Bind to allosteric sites
What is the purpose of spare receptors?
EC50
What is intrinsic activity?
The ability of a drug to activate a receptor
Give a clinical example where differences in affinity and efficacy are important
In asthma, treatment goal is to activate B2-adrenoreceptors to relax the airways but there are B-adrenoreceptors elsewhere in the body e.g. B1 in heart increases force and rate.
Salbutamol
- high Kd for B1 and low Kd for B2
- therefore has higher affinity for B2
- there is also selectivity for B2 through the route of administration (oral spray)
Salmeterol
- longer acting than salbutamol
- no selective efficacy so relies on prevention of B1 activation surely through differences in affinity
- 3500x greater affinity got B2