Introduction to Pharmacology Quiz
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Questions and Answers

What is the process of absorption in pharmacology?

  • Breaking down of the drug in the liver
  • Transport of drugs to the target organs
  • Elimination of the drug from the body
  • Uptake of the drug from the application site into the bloodstream (correct)

What does the distribution of a drug involve?

  • Transport between the bloodstream and other body tissues (correct)
  • Excretion of the drug from the body
  • Conversion of the drug to its metabolites
  • Inactivation of the drug by the liver

What role does metabolism play in drug processing?

  • How much of the drug is absorbed into the bloodstream
  • Its distribution across various tissues
  • How much of the drug is broken down in the liver (correct)
  • Its effect on the target cells

Which process describes the elimination of drugs from the body?

<p>Excretion (B)</p> Signup and view all the answers

Which of the following statements is NOT true regarding drug metabolism?

<p>It is limited to the chemical breakdown of drugs (A)</p> Signup and view all the answers

What is the primary use of Zocor?

<p>Reduces cholesterol levels (D)</p> Signup and view all the answers

Which drug is classified as a generic name for Tylenol?

<p>Acetaminophen (B)</p> Signup and view all the answers

Which of the following medications is used to manage type 2 diabetes?

<p>Glucophage (B)</p> Signup and view all the answers

Prilosec is primarily used to treat which of the following conditions?

<p>Gastroesophageal reflux disease (GERD) (C)</p> Signup and view all the answers

What combination of drugs does Adderall contain?

<p>Amphetamine and Dextroamphetamine (A)</p> Signup and view all the answers

What term describes the effects that a drug has on the body?

<p>Pharmacodynamics (D)</p> Signup and view all the answers

Which term refers to how the body processes a drug?

<p>Pharmacokinetics (B)</p> Signup and view all the answers

What does the acronym ADME stand for in relation to drug delivery?

<p>Absorption, Distribution, Metabolism, Elimination (C)</p> Signup and view all the answers

Which of the following factors determines whether a drug reaches its site of action?

<p>ADME (B)</p> Signup and view all the answers

In pharmacokinetics, which component does NOT belong to the ADME factors?

<p>Efficacy (A)</p> Signup and view all the answers

What is the primary effect of inhibition on specialized cells?

<p>Selective reduction in activity (D)</p> Signup and view all the answers

Which of the following substances is known for its inhibitory effect on the central nervous system?

<p>Barbiturates (A)</p> Signup and view all the answers

What type of drugs are considered sedative-hypnotics due to their inhibitory effects?

<p>Barbiturates (C)</p> Signup and view all the answers

How does inhibition commonly affect the activity of specialized cells?

<p>It manifests as a specific reduction in activity (C)</p> Signup and view all the answers

Which of the following is NOT associated with the concept of inhibition?

<p>Increased neuronal activity (A)</p> Signup and view all the answers

What is the primary action of NSAIDs like aspirin and naproxen?

<p>Inhibit cyclooxygenase (D)</p> Signup and view all the answers

Which class of drugs is responsible for inhibiting the angiotensin converting enzyme?

<p>ACE inhibitors (C)</p> Signup and view all the answers

What is the effect of inhibiting cyclooxygenase in the context of NSAID use?

<p>Reduces pain and inflammation (C)</p> Signup and view all the answers

What type of inhibition do organophosphates exert on cholinesterase?

<p>Irreversible inhibition (B)</p> Signup and view all the answers

Captopril and Enalapril are primarily used to manage which condition?

<p>High blood pressure (A)</p> Signup and view all the answers

Which of the following is NOT a characteristic of NSAIDs like aspirin and naproxen?

<p>They increase prostaglandin production (D)</p> Signup and view all the answers

What is the primary role of ion channels in cellular processes?

<p>To regulate the influx and outflux of ions (B)</p> Signup and view all the answers

Which of the following best describes the action of organophosphates on cholinesterase?

<p>Causing irreversible damage (B)</p> Signup and view all the answers

Which mechanism does NOT characterize the function of ion channels?

<p>Transporting large molecules (A)</p> Signup and view all the answers

The inhibition of cholinesterase by organophosphates primarily results in which consequence?

<p>Prolonged action of neurotransmitters (D)</p> Signup and view all the answers

Flashcards

Generic Name of Viagra

The non-proprietary name for a drug, used in medical documentation and prescriptions; in this case, Sildenafil.

Pharmacodynamics

How a drug affects the body.

Brand Name of Acetaminophen

A proprietary name given by a pharmaceutical company. This one is Tylenol.

Pharmacokinetics

How the body affects a drug.

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Drug Classification

A way to group similar drugs based on their chemical makeup, mechanism of action or therapeutic use.

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ADME

Factors determining if a drug reaches its target.

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Generic Name

The official non-proprietary name for a medication.

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Absorption

Process of drug entering the bloodstream.

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Distribution

How a drug moves throughout the body.

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Simvastatin's Use

A medication used to lower cholesterol levels, also known as Zocor in the market.

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What is Absorption?

The process by which a drug enters the bloodstream from where it was applied, like a pill or injection.

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Metabolism

The process of breaking down a drug in the liver.

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Elimination

The process of removing a drug from the body, often via urine or feces.

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Liver's Role

The liver is responsible for metabolizing drugs, breaking them down into smaller, easier-to-eliminate compounds.

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Inhibition

A process where the activity of specific cells is reduced or suppressed. This can occur in various parts of the body and can be caused by different mechanisms.

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Inhibition: Effect on CNS

When a drug has an inhibitory effect on the central nervous system (CNS), it can slow down brain activity, leading to sedative or hypnotic effects.

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Example of CNS Inhibition

Barbiturates are a class of drugs that work by inhibiting the activity of the CNS, leading to sedative-hypnotic effects. This means they can calm the nervous system and induce sleep.

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What is CNS Inhibition?

CNS inhibition is a process where the activity of the central nervous system is reduced, potentially leading to relaxed states, drowsiness, or sleep.

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How do Barbiturates Work?

Barbiturates work by acting on the CNS to produce sedative (calming) and hypnotic (sleep-inducing) effects.

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NSAIDs

Nonsteroidal Anti-inflammatory Drugs like aspirin and naproxen that reduce inflammation by blocking the production of prostaglandins.

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Prostaglandins

Hormone-like substances produced by the body that play a role in inflammation, pain, and fever.

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ACE Inhibitors

Drugs like Captopril and Enalapril that lower blood pressure by blocking the conversion of angiotensin I to angiotensin II, a powerful vasoconstrictor.

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Angiotensin II

A powerful hormone that constricts blood vessels, leading to an increase in blood pressure.

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Vasoconstriction

Narrowing of blood vessels, which increases blood pressure.

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Irreversible Inhibition

When a drug permanently disables an enzyme, preventing it from functioning normally.

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Organophosphates

A type of chemical that can irreversibly inhibit cholinesterase, an enzyme crucial for nerve function.

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Cholinesterase

An enzyme vital for nerve transmission, breaking down acetylcholine, a neurotransmitter.

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Ion Channel

A protein embedded in cell membranes allowing ions to pass through, controlled by specific signals.

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Concentration Gradient

The difference in concentration of a substance across a membrane, driving movement from high to low concentration.

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Study Notes

Introduction to Pharmacology

  • Pharmacology is the science of drugs, their effects on living organisms (including humans and animals), and their safety and effectiveness.
  • A drug is any substance used for diagnosis, prevention, or relief/cure of diseases in humans or animals.
  • A drug can be defined legally as any agent approved by the Drug Control Authority for treating or preventing diseases.
  • Socially, a drug can be any substance that is disapproved or illegal and can be associated with addictive, narcotic, or mind-altering substances.
  • Drugs are needed when physiology is compromised by a disease state.

Basic Definitions

  • Drug nomenclature refers to the naming of drugs.
  • Pharmacy is the art and science of compounding and dispensing drugs; preparing suitable dosage forms for administration.
  • Pharmacodynamics is the study of what a drug does to the body.
  • Pharmacokinetics is the study of what the body does to a drug.
  • Toxicology examines poisonous effects of a drug with emphasis on detection and treatment of poisonings, including adverse drug effects.
  • Clinical pharmacology involves the application of pharmacodynamic and pharmacokinetic principles to treat diseases.
  • Pharmacotherapeutics is the application of pharmacological information with the knowledge of a disease for its prevention or cure. It includes selecting appropriate drug doses.
  • The large-scale manufacturing of drugs is called pharmaceutics which is primarily a technological science.

Drug Sources

  • Drugs can be synthetic chemicals or derived from natural sources like plants, microbes, or animal tissues, and minerals.
  • Plants can yield alkaloids (morphine) and microbes can produce antibiotics (penicillin).
  • Animal tissues can furnish hormones (growth hormone, insulin).
  • Minerals like lithium are used in psychotherapy.

Drug Nomenclature

  • Trade names are exclusive names given to drugs by the manufacturer. Examples include Panadol®, Tylenol®, Uphamol®.
  • Chemical names describe the chemical composition and molecular structure of the drug. For example, N-Acetyl-p-aminophenol.
  • Generic names are official names for international non-proprietary medications that are not manufacturer-specific like Paracetamol or acetaminophen.
  • Generic names, rather than trade names, should be used when possible in clinical practice.

Drug Classification

  • Drugs are classified according to therapeutic use, the mechanism of action, site of action and chemical structure, and pharmacokinetic sub-classification (short/long-acting).
  • Common examples include antidiabetics (e.g., insulin), antihypertensives, and anticancer drugs.
  • Antidiabetic drugs can involve insulin, sulphonylureas, meglitinides, Biguanides, and more, each with associated adverse effects

Antihypertensive Drug Classes

  • Antihypertensive drug classes include ACE inhibitors ("pril"), ARBs ("sartan"), alpha blockers ("osin"), beta blockers ("lol"), Calcium channel blockers ("dipine"), and diuretics ("ide").
  • Each class targets specific mechanisms to reduce blood pressure.

Anticancer Drugs

  • Anticancer drugs have variations in modes of action. Classification includes alkylating agents, antimetabolites, plant-derived drugs, and microtubule-damaging agents. Different classes directly target different processes in cancer cells to reduce malignancy, for example, platinum coordination complexes.

Types of Drug Action

  • Drug action can be classified as stimulation, depression, irritation, replacement, or cytotoxic.
  • Examples of stimulation include adrenaline for cardiac arrest, and pilocarpine for dry mouth.
  • Barbiturates are examples of antidepressants, and Quinidine is an example of an antiarrhythmic drug.
  • Cytotoxic drugs are utilized against invading bacteria, parasites, and cancer cells. Examples include penicillins, chloroquine, Zidovudine (anti-HIV), and cyclophosphamide.

Mechanism of Drug Action

  • Drugs can affect the body by altering specific biological processes such as physical action, chemical action, and interacting with target biomolecules like enzymes, ion channels, transporters, and receptors.
  • Examples of physical actions include bulk laxatives, adsorbants, and mannitol.
  • Examples of chemical actions include antacids and chelating agents.
  • These methods change the way that drugs and the body interact to allow for changes to occur, like reducing blood pressure.

Clinical Studies

  • Clinical studies evaluate drug action in humans in four stages commonly referred to as phases.
  • Phase I trials usually involve small groups of healthy volunteers and evaluate safety and pharmacological properties.
  • Phase II trials focus on smaller groups of patients with the disease and evaluate efficacy, and identify appropriate doses.
  • Phase III trials test efficacy and safety within larger groups of patients with the disease to compare a drug to a placebo.
  • Phase IV trials involve post-marketing surveillance and evaluate long-term effects and risks.
  • Pharmacovigilance is a critical aspect of clinical drug development to monitor and report adverse effects of drugs after they have been launched in the market.

Pharmacology Work Types

  • Experimental pharmacology involves evaluating drug action in animals to determine drug efficacy and safety before human trials. This also involves clinical pharmacology which evaluates drug actions in humans, to understand more about responses.

Where receptors are Located

  • Receptors, which are proteins that receive signals from other molecules in the body, are located in several parts of the cell to enable the interaction between drugs and the body.
  • These include cell membranes, cytoplasm and nucleus.

Other Relevant terms

  • Drug: a substance used for diagnosis, prevention, or relief or cure of diseases.
  • Medicine: a drug used for therapeutic purpose.
  • Pharmacology: science of drugs, their effects, and safety/effectiveness.
  • Pharmacokinetics: how the body processes a drug.
  • Pharmacodynamics: the study of what a drug does to the body.
  • Toxicology: study of poisonous effects of drugs.

The Thalidomide Disaster

  • Thalidomide was a widely used sleeping pill.
  • It caused birth defects in a large proportion of exposed fetuses.
  • This disaster was instrumental for heightened caution in modern drug development, causing modern testing for teratogenicity.

Additional Information

  • The presented information is a brief overview of an extensive subject; further research is highly recommended for in-depth understanding.

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Test your knowledge on the fundamentals of pharmacology, including definitions, drug nomenclature, and the basic principles of pharmacodynamics and pharmacokinetics. Explore how drugs interact with living organisms and the safety and effectiveness of these substances. Sharpen your understanding of both legal and social definitions of drugs.

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