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Questions and Answers
Which of the following best describes pharmacodynamics?
Which of the following best describes pharmacodynamics?
- Drug absorption in the body
- The effect of a drug on the body (correct)
- The effect of the body on the drug
- Drug elimination from the body
Pharmacokinetics describes the toxic effects of drugs.
Pharmacokinetics describes the toxic effects of drugs.
False (B)
What term refers to a chemical substance that can affect a biological system?
What term refers to a chemical substance that can affect a biological system?
drug
A receptor is a protein that receives chemical messages, also known as a(n) _______.
A receptor is a protein that receives chemical messages, also known as a(n) _______.
Match the following terms with their descriptions:
Match the following terms with their descriptions:
What is the first step in cell communication?
What is the first step in cell communication?
In autocrine signaling, a cell sends a signal to a remote cell.
In autocrine signaling, a cell sends a signal to a remote cell.
A receptor is a macromolecule structure made of ______ chains.
A receptor is a macromolecule structure made of ______ chains.
What is another name for a ligand?
What is another name for a ligand?
What is the outcome of a ligand (signaling molecule) binding to a receptor (signal detector)?
What is the outcome of a ligand (signaling molecule) binding to a receptor (signal detector)?
Flashcards
Pharmacodynamics
Pharmacodynamics
The study of how drugs affect the body and their mechanisms of action.
Pharmacokinetics
Pharmacokinetics
Describes how the body affects a drug, including absorption, distribution, metabolism, and elimination.
Drug
Drug
A chemical substance that can affect biological systems, either natural or synthetic.
Cell signaling
Cell signaling
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Ligand
Ligand
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Cell signaling steps
Cell signaling steps
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Receptor
Receptor
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Signal transduction
Signal transduction
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Types of cell signaling
Types of cell signaling
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Study Notes
Lecture 1: Introduction to Pharmacology: Pharmacodynamics
- Pharmacology definition: The study of the interaction between a chemical substance and a living system (pharmakon = drug or poison, ologos = science).
- Drug definition: A chemical substance, natural or synthetic, affecting a biological system (human, animal, insect, or cell).
- Pharmacology subdivisions:
- Pharmacodynamics: Describes the effect of a drug on the body and the mechanism of its action (receptor binding or interactions).
- Pharmacokinetics: Describes the effect of the body on the drug, determining how quickly and to what extent it appears at the target site (absorption, distribution, metabolism, elimination).
- Pharmacotherapeutics: The clinical use and indications for a drug.
- Toxicology: The study of the toxic effects of drugs or toxins.
- Cell signaling: How cells communicate, either electrically (neural transmission) or chemically (ligands, e.g., hormones, neurotransmitters).
- Ligand: A small molecule interacting with a specific receptor site.
- Types of cell signaling (based on distance):
- Autocrine: Signal from a cell to itself.
- Paracrine: Signal from a cell to a neighboring cell
- Endocrine: Signal from a cell to a distant cell.
- Three types of cell surface receptors:
- Ligand-gated ion channels: Ligand binding opens or closes a channel, altering ion flow, leading to rapid response (e.g., milliseconds).
- G protein-coupled receptors (GPCRs): Ligand binding activates a G protein, which in turn activates another enzyme, leading to a cascade of effects with a response time of seconds to minutes.
- Enzyme-linked receptors: Ligand binding activates an intracellular enzyme, leading to a longer response lasting minutes or hours.
- Intracellular receptors (DNA-linked receptors): Lipid-soluble ligands cross the membrane and bind to intracellular receptors which regulate gene expression, resulting in a delayed response (hours or days).
- Drug Affinity: The ability of a drug to bind to a specific receptor (determined by the strength of bonds and their number).
- Drug Efficacy (Intrinsic Activity): The ability of a drug to produce a biological effect, related to the number of drug-receptor complexes formed, with a maximal response reached when all receptors are occupied.
- Non-receptor-mediated effects: Some drugs exert effects via interactions not involving receptors (e.g., antacids, osmotic diuretics).
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Description
Explore pharmacodynamics, a pharmacology subdivision describing the effects of drugs on the body and their mechanisms of action. It includes receptor binding and cell signaling. Learn how drugs interact with biological systems.