Drug-Receptor Interactions Flashcards
Define Pharmacokinetics and Pharmacodynamics.
Pharmacokinetics – the effect that the body has on the drug
Pharmacodynamics – the effect of the drug on the body
Define the word ‘drug’.
A chemical substance that interacts with a biological system to produce a physiological response
State the four main target sites for drugs.
Receptors
Ion Channels
Transport Systems
Enzymes
What are the two types of ion channels?
Voltage-Gated
Receptor Linked
Give an example of a group of drugs that act on ion channels.
Local anaesthetics – they block the voltage gated sodium channels of nociceptor neurons to prevent the conduction of pain signals to the CNS
Give an example of a drug that acts on transport systems.
Tricyclic antidepressants
Cardiac glycosides – it slows down the Na+/K+ pump thereby increasing the intracellular calcium ion concentration, which leads to an increased force of contraction
What are the three ways in which drugs can interact with enzymes?
Enzyme inhibitors (e.g. anticholinesterases) False transmitter (e.g. methyldopa) Prodrugs (e.g. chloral hydrate)
What is a common example of the unwanted effects of drug interaction with enzymes?
Paracetamol overdose – this will saturate the microsomal enzymes in the liver so the paracetamol is then broken down by another set of enzymes (P450) which generates toxic metabolites
Name three groups of drugs that are exceptions to the four target site rule.
General anaesthetics – reduce synaptic transmission without interacting with transport systems or receptors
Antacids – these are basic so they simply neutralize some of the stomach acid
Osmotic purgatives – draw water into the bowel due to its physicochemical properties
Define agonist.
A molecule that binds to a receptor and generates a response
Define antagonist.
A molecule that binds to a receptor but do NOT generate a response
Define potency. What is it dependent on?
How powerful the drug is
It depends on affinity (how willingly the drug binds to the receptor) and efficacy (the ability of a drug to generate a response once bound)
What is a full agonist?
An agonist that generates a maximum response
What is a partial agonist?
An agonist that generates a less than maximum response
What is selectivity?
Drugs have a preference for binding to certain receptors (it is rarely specific – they normally bind to a few different receptors)