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CHEM358 Pharmacodynamics Chapter 2 Quiz
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CHEM358 Pharmacodynamics Chapter 2 Quiz

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Questions and Answers

What is the primary focus of the Dose-Effect model?

  • The theory behind receptor-drug interactions
  • The association/dissociation of drugs at equilibrium
  • The relationship between dose and effect (correct)
  • Comparisons between medications for the same indication
  • Which statement best describes the necessity of understanding dose-effect relationships?

  • Facilitate comparisons between drugs for different indications
  • Predicting the rate of drug degradation in the body
  • Ability to predict the effects of changing dose of a drug (correct)
  • Enhance understanding of how drugs are synthesized
  • In the Dose-Effect model, what is the response proportional to at equilibrium?

  • Plasma concentration of the drug
  • Rate of drug elimination
  • Number of receptors occupied (correct)
  • Frequency of drug administration
  • What does 'Max response = 10 a.u.' indicate in the context of drug-receptor interactions?

    <p>Maximum receptor occupancy reached by the drug</p> Signup and view all the answers

    Which factor primarily determines the magnitude of response in the Dose-Effect model?

    <p>Number of receptors occupied</p> Signup and view all the answers

    What role does equilibrium play in drug-receptor interactions?

    <p>Balances the association and dissociation of drugs with receptors</p> Signup and view all the answers

    In the context of drug-receptor interactions, what does Ntot represent?

    <p>Total number of receptors present in the tissue</p> Signup and view all the answers

    What is the equilibrium constant for association (K) defined as?

    <p>The ratio of free drug to free receptor concentrations at equilibrium</p> Signup and view all the answers

    How do pharmacologists define the equilibrium constant for dissociation (KA)?

    <p>As the reciprocal of the ratio of drug-receptor complex to free drug and receptor</p> Signup and view all the answers

    What does the magnitude of response at equilibrium depend on in drug-receptor interactions?

    <p>The number of receptors occupied by the drug</p> Signup and view all the answers

    How does the dose-effect model describe the relationship between receptor occupancy and response?

    <p>It is non-linear and inversely proportional</p> Signup and view all the answers

    What is the purpose of defining the equilibrium constant for dissociation in terms of reciprocal units (mol/L)?

    <p>To make it easier to understand by using simpler units</p> Signup and view all the answers

    In the context of receptor occupancy, what does a lower KA value signify?

    <p>Higher drug affinity for the receptor</p> Signup and view all the answers

    What can be inferred about the response from the fractional occupancy equation pA = A [A] / (A [A] + KA)?

    <p>Response increases with higher fractional occupancy</p> Signup and view all the answers

    How is the relationship between free agonist [A] and fractional occupancy (pA) visualized?

    <p>Sigmoidal plot</p> Signup and view all the answers

    What is the significance of pA = A [A] / (A [A] + KA) in pharmacology?

    <p>Describing drug-receptor affinity</p> Signup and view all the answers

    How does maximum possible response relate to receptor occupancy?

    <p>Maximum response is achieved at 50% occupancy</p> Signup and view all the answers

    Why is a sigmoidal plot preferred for extracting information in pharmacology over a hyperbolic plot?

    <p>Sigmoidal plots are easier to interpret</p> Signup and view all the answers

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