Pharmacodynamics Flashcards

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This set of vocabulary flashcards covers the fundamental principles of pharmacodynamics, including receptor types, signaling mechanisms, and drug interaction properties as presented by Dr. Claire Kelly.

Last updated 6:24 AM on 5/18/26
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18 Terms

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Pharmacodynamics

The study of how a drug effects biochemical, molecular, and physiological processes at the cellular and organ level; often described as "what the drug does to the body."

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Agonist

A ligand that binds to a receptor and produces a biological response.

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Antagonist

A ligand that binds to a receptor but produces no response, effectively blocking the primary ligand.

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Ligand-gated ion channels

Receptors where the binding of a ligand (such as a neurotransmitter) opens a channel to allow rapid effects; examples include AchAch (excitatory) and GABAGABA (inhibitory).

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G-protein coupled receptors (GPCRs)

The largest and most diverse family of receptors consisting of three subunits (αβγ\alpha\beta\gamma).

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α\alpha subunit

The part of a G-protein that functions as a GTPase and is linked to effector enzymes, channels, or carrier proteins.

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Adenylate Cyclase (ACAC)

A GPCR effector enzyme that produces cAMPcAMP, which then activates protein kinase A (PKAPKA).

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GαsG\alpha_s

A stimulatory G-protein subunit.

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GαiG\alpha_i

An inhibitory G-protein subunit.

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Phospholipase C (PLCPLC)

A GPCR effector linked to signaling through IP3IP_3, DAGDAG, and the α1\alpha_1-adrenoreceptor.

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Enzyme-linked receptors

Receptors important for hormones, growth factors, and cytokines (e.g., Insulin) that typically dimerise and are coupled to kinases like receptor tyrosine kinases.

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Nuclear Receptors

Ligand-activated transcription factors that interact with DNA directly to modify transcription; their ligands are normally lipid-soluble, such as endocrine steroid hormones.

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Selectivity

A factor affecting receptors that refers to their ability to bind to either a single or multiple ligands.

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Affinity

The strength of a drug-receptor interaction.

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Intrinsic activity (efficacy)

The ability of a drug-receptor interaction to produce a physiological response.

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Upregulation

The regulation process where receptor sensitivity or number increases, as seen with Propranolol.

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Downregulation

The regulation process where receptor sensitivity or number decreases, as seen with Salbutamol.

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JAK-STAT-kinase

A specific type of kinase pathway associated with enzyme-linked receptors.