Principles of pharmacology Flashcards
Give examples of drugs which produces their effects due to their physiochemical properties
- Antacids- i.e. sodium bicarbonate, base- increases pH, counters indigestion
- Bulk laxatives- i.e. methylcellulose, not absorbed, streches gut wall, relieves constipation
- Osmotic laxatives- i.e. magnesium sulfate, increases the aount of water in faeces
- Osmotive diuretics- i.e. mannitol, give by IV, fltered in kidneys, ot reabsorbed into bloodstream leading to more urine
- General anesthetic- i.e. halothane, lipid soluble thus interats with lipids in the cell membrane, renders individual unconcious
- Alcohol- acts as a general anaesthetic
What is meant by the potency of a drug?
- Potency is the measure of drug activity in a biological system
- high potency means effective at very low concentrations
What is meant by specificity of a drug?
- Chemical specificity- drug wise
- drugs are specific and complimetary to their receptor
- Biological specificity- receptor wise
- receptors are located on different tissues
- lead to different effects
What is an agonist?
Bind to a receptor and produce a response
possess affinity and efficacy
- i.e.acetylcholine, histamine
What is an antagonist?
- binds to a rece[tpr but do not produce a response
- prevent agonist binding and so block the response to an agonist
- possess affinity but not efficacy
- i.e. atropine, mepyramine
What are the three types of antagonists?
- Competitive
- Irreversible
- Other
What is meant by quantitative pharmacology?
based on the assuption that drugs act by entering int a simple chemical relation with certain receptors in cells and that there is a simple relation between the amount of drug fixed by these receptors and the action produced
What is the relationship between drug concentration and response?
- Graded- the level of increase in response chages as concentration changes
- Saturating- the maimum response cannot be exceeded
- exhibits threshold- minimum concentration required for effect
Assumption- ‘response’ = concentration of drug recepor complexes