Anesthesia Vocabulary Flashcards
Agonist
A drug that activates a receptor by binding to it and initiating a biological response
Antagonist
A drug that binds to a receptor without activating it, thereby block- ing the receptor from being activated by other substances.
Competitive antagonism
A type of antagonism where the antagonist inhibits the response of an agonist by competing for the same receptor binding site.
Non-competitive antagonism
A type of antagonism where the antagonist binds to a different site on the receptor, making it less responsive to agonists even at high concentrations.
Partial agonists
Drugs that activate receptors but to a lesser extent than full ago- nists, resulting in a partial biological response.
Inverse agonists
Drugs that induce the opposite effect of an agonist by binding to the same receptor site and producing a negative response.
Tolerance
A decreased response to the same dose of a drug over time, requiring higher doses to achieve the same effect.
Pharmacokinetics
The quantitative study of how drugs are absorbed, distributed, metabolized, and excreted by the body.
Central volume
The volume of distribution at steady state for anesthetics, which reflects their distribution throughout the central compartment of the body.
Vessel rich group
The primary targets for bolus injection of anesthetics, including the brain, heart, kidneys, and liver, which have a high blood flow.
Zero-order processes
Processes in which the rate of elimination or consumption of a drug remains constant regardless of the drug concentration.
First-order processes
Processes in which the rate of elimination of a drug is proportional to the total amount of drug present in the body.
Elimination Half-time
The time required for the plasma concentration of a drug to de- crease by half during a constant concentration infusion or after a bolus dose.
Elimination Half-life
The time it takes for the concentration of a drug in the body to decrease by 50% through elimination processes.
Context-sensitive half-time
The time required for the blood plasma concentration of a drug to decrease by 50% after discontinuation, taking into account the drug’s elimination characteristics.
Clearance
The amount of drug that is extracted by an organ per unit of time, indicating the organ’s ability to eliminate the drug.
Pharmacodynamics
The study of how drugs interact with the body and produce their effects, including the intrinsic sensitivity or response of the body to a drug.