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These flashcards cover key concepts from pharmacodynamics, including definitions, drug action theories, dose-response relationships, and types of receptors and interactions.
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Pharmacodynamics (PD) is defined as __.
The study of the biochemical and physiological effects of drugs and their mechanisms of action.
The primary focus of pharmacodynamics is __.
What the drug does to the body.
The study of how the body affects drugs is referred to as __.
Pharmacokinetics (PK).
Drug action is often mediated through __.
Receptors.
Receptor binding translates into __.
Pharmacologic effect.
The __ curve shows the relationship between drug dose and effect.
Dose-response.
Key drug properties assessed in dose-response curves include __, potency, and efficacy.
Emax.
A __ agonist is a drug that activates a receptor to produce a maximal effect.
Full.
An __ agonist binds to a receptor but produces a submaximal effect.
Partial.
An __ antagonist blocks a receptor but does not activate it.
Antagonist.
In receptor occupancy theory, __ refers to the fraction of receptors bound by a drug.
Occupancy.
Drugs that bind at sites other than the orthosteric site are called __ modulators.
Allosteric.
The intrinsic activity of a drug is also known as its __.
Efficacy.
The __ index (TI) is a measure of a drug's safety margin.
Therapeutic.
Efficacy versus __ is a key distinction in pharmacodynamics.
Potency.
The __ dose (ED50) is the dose effective in 50% of individuals.
Median effective.
In a graded dose-response curve, the x-axis represents the __.
Drug dose.
Specific binding sites for drugs on biological macromolecules are called __.
Receptors.
__ receptors are proteins that bind ligands and transduce signals.
Signal-transducing.
The effects of a drug on a biological system depend on its __ and its mechanisms of action.
Chemical actions.
The __ is a measure of the ratio between the dose causing toxic effects and therapeutic effects.
Therapeutic index (TI).
An increase in drug concentration causes a __ in receptor occupancy.
Increase.
Partial agonists function by __ both agonism and antagonism to a receptor.
Mediating.
The relationship between receptor occupancy and pharmacological response follows __ theory.
Occupancy.
Drugs acting away from the active site may either enhance or inhibit receptor function and are known as __.
Allosteric drugs.
The __ effect is defined as the maximum response a drug can produce regardless of the dose.
Emax.
A __ antagonist binds reversibly to the active site, competing with the agonist.
Competitive.
Drugs that produce effects quickly fall under the category of __ pharmacodynamics.
Fast.
The __ curve illustrates diverse responses within a population to a drug.
Quantal.
The term __ refers to drugs that enhance the effects of another drug.
Agonists.
Drugs like __ that bind to the GABA_A receptor enhance inhibitory effects.
Benzodiazepines.
Drugs that decrease activity of a target are known as __.
Inhibitors.
The __ response measures continuous drug effects in a single subject.
Graded.
Spare receptors allow for __ response even when not all receptors are activated.
Maximal.
Dose–response relationships can inform __ regimens.
Dosing.
__ effects occur with repeated use of a drug over a longer time.
Tolerance.
Rapid decreases in drug effect after repeated doses manifest as __.
Tachyphylaxis.
The term __ delineates how selectively a drug binds to its target receptor.
Selectivity.
Non-covalent (reversible) drug interactions include various types of molecular bonds like __ bonds.
Hydrogen.
Understanding __ relationships helps identify therapeutic windows for drug application.
Dose-response.
The __ of a drug's effects marks the critical point for its therapeutic application.
Maximal efficacy.
In pharmacodynamics, efficacy is characterized as the __ of a drug to produce a response.
Ability.
Drugs that outcompete natural ligands are often categorized based on their __ effects.
Antagonistic.
A dose-response curve shows how much drug is needed for a defined __.
Effect.
A __ agonist stabilizes receptor activity below baseline.
Inverse.
Understanding __ is critical for predicting drug interactions within the body.
Drug selectivity.
Receptor-mediated mechanisms form the basis of __ theory.
Binding.
Factors such as receptor can influence the pharmacodynamics of a drug.
Density.