Concepts of Pharmacology Flashcards
Pharmacokinetics
what the body does to drugs
Pharmacodynamics
what drugs do to the body
Types of drug receptors
Membrane lock and key (Beta Adrenergic Receptor) Ligand-gated ion channel (GABA) Voltage-gated ion channel (Na+ channel) Intracellular Enzymes (Phosphodiesterase Inhibitors)
Enantiomers
2 molecules having the same chemical composition but different orientations around a central atom - mirror images
Agonist
Drug that produces its clinical effect by binding to a receptor and activating it (mimetics)
Antagonist
Drugs that bind to receptors and inhibit them from binding to drugs that activate them. Competitive inhibition.
Direct Agonism
Drugs that bind directly with a receptor to trigger physiologic response
Indirect Agonism
Drugs that produce physiologic responses by increasing the concentration of Endogenous substrate such as neurotransmitters and hormones at the receptor site.
Competitive Antagonism
Inhibits receptors from binding to agonists. Can be overcome by increasing the concentration of agonists at receptor sites.
Non-competitive Antagonism
Inhibits receptors from binding to agonists. Cannot be overcome by increasing the concentration of the agonist.
Compartment Theory
Body is composed of multiple compartments with set volumes. Examining the pharmacokinetics of drugs in terms of what compartment they travel to.
2 Compartment Model
Central Compartment - rapid uptake, intravascular fluid, and perfused tissues like the lungs, heart, brain, kidneys and liver. 75% of cardiac output to 10% of body mass.
Peripheral Compartment - slow uptake, includes less vascular tissues like fat, bone, and inactive skeletal muscle.
Eventually equilibrated and eliminated from central compartment.
Plasma Concentration/Diffusion
Immediately after administration of drug diffuses from central to peripheral compartments.
Protein Binding
Many drugs travel through the blood attached to proteins like Albumin and alpha-1-acid glycoproteins.
Degree of binding is inversely proportional to volume of distribution.
Biotransformation
Chemical process by which drugs are altered in the body. Can be set into two phases.
Phase I: Convert to polar metabolite
Phase II: Conjugate with endogenous substrate to water soluble.