chapter two
Chapter 2: Drugs and the Body
Pharmacodynamics
Definition:
Pharmacodynamics is the study of interactions between chemical components of living systems and foreign chemicals (including drugs) that enter these systems.
When a new chemical enters a biological system, it can alter the function of cells, leading to multiple physiological changes.
Drug Actions
Possible Actions of Drugs:
Replacing or acting as a substitute for missing chemicals in the body.
Increasing or stimulating certain cellular activities to enhance physiological functions.
Depressing or slowing cellular activities, thereby reducing various physiological responses.
Interfering with the functioning of foreign cells, which may help combat infections or other pathological conditions.
Receptor Sites
Definition and Function:
Receptor sites are specific areas on cell membranes that react with certain chemicals and produce effects within the cell.
Types of Drugs Interacting with Receptor Sites:
Agonists:
Drugs that bind to receptor sites and induce a response in the cell.
Competitive Antagonists:
Drugs that bind to the same receptor sites as agonists but do not activate them, thereby blocking the action of the agonists.
Noncompetitive Antagonists:
Drugs that bind to different receptor sites and inhibit the action of agonists without competing for the same binding site.
Partial Agonists:
Drugs that bind to receptor sites but produce a weaker response compared to full agonists.
Drug-Enzyme Interactions:
Drugs may interact with enzymes in ways that affect metabolic processes.
Selective Toxicity:
The ability of a drug to selectively target pathological cells while sparing healthy cells.
Key Interaction Examples
Lock and Key Metaphor:
Drug A (Agonist): Binds to receptor sites, producing effects.
Drug B: Cannot bind to receptor sites, thus has no effect.
Drug C (Antagonist): Binds to the same receptor site as Drug A, preventing it from binding.
Drug D (Competitive Antagonist): Binds to a different receptor site but inhibits Drug A's actions.
Pharmacokinetics
Definition:
Pharmacokinetics is the study of the absorption, distribution, metabolism (biotransformation), and excretion of drugs.
Key Processes in Pharmacokinetics
Onset of Drug Action:
Refers to the time it takes for a drug to begin its therapeutic effect.
Drug Half-Life:
The time required for the concentration of a drug in the body to decrease to half its initial amount.
Timing of Peak Effect:
Refers to the time when the drug reaches its maximum therapeutic effect.
Duration of Drug Effects:
The length of time a drug maintains its therapeutic effects before additional doses are needed.
Metabolism/Biotransformation of the Drug:
The chemical modification made by an organism on a chemical compound, primarily occurring in the liver.
Site of Excretion:
Refers to organs responsible for removing drugs from the body, primarily the kidneys.
Pharmacokinetics Flow
Processes Involved:
Drug Dose Administration Method:
Drug can be administered through various routes (e.g., GI tract, muscle, subcutaneous tissue).
Drug Distribution:
Drugs travel through blood plasma to target tissues; distribution influenced by properties like lipid solubility and blood flow.
Tissue Storage Sites:
Drugs can accumulate in fat or protein tissues.
Excretion Mechanism:
Drugs are excreted primarily via kidneys, bile, lungs, and other pathways.
Important Pharmacokinetic Concepts
Critical Concentration:
The minimum amount of drug required to achieve a desired therapeutic effect.
Loading Dose:
Typically a higher initial dose administered to rapidly reach critical concentration.
Dynamic Equilibrium:
The state at which the amounts of drug absorbed, distributed, metabolized, and excreted balance out.
Dynamic Equilibrium
Components that Contribute to Dynamic Equilibrium:
Absorption
Distribution
Biotransformation
Excretion
Absorption
Definition:
The process by which a drug moves