Adrenergic Drug Quiz

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Questions and Answers

Which enzyme metabolizes catecholamines in the synaptic space?

  • Both COMT and MAO
  • Catechol-O-methyltransferase (COMT) (correct)
  • Neither COMT nor MAO
  • Monoamine oxidase (MAO)

Which type of receptors do catecholamines potently activate?

  • Neither α nor β receptors
  • α receptors
  • Both α and β receptors (correct)
  • β receptors

Which of the following is NOT a catecholamine?

  • Epinephrine
  • Norepinephrine
  • Isoproterenol
  • Phenylephrine (correct)

Which type of drugs are sympathomimetic amines that contain the 3,4-dihydroxybenzene group?

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

Which receptors have a higher potency for isoproterenol compared to epinephrine and norepinephrine?

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

Flashcards

Catechol-O-methyltransferase (COMT)

An enzyme responsible for breaking down catecholamines in the synaptic space.

Alpha and Beta Receptors

Catecholamines primarily bind to and activate these receptors.

Phenylephrine

This drug does not belong to the catecholamine family.

Catecholamines

These drugs share a common structural feature and act as stimulants.

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Isoproterenol

This drug has a stronger attraction to beta receptors compared to alpha receptors.

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Study Notes

Enzyme and Metabolism

  • Catechol-O-methyltransferase (COMT) metabolizes catecholamines in the synaptic space, playing a critical role in neurotransmitter regulation.

Receptors Activated by Catecholamines

  • Catecholamines, such as dopamine, norepinephrine, and epinephrine, potently activate adrenergic receptors, which are divided into alpha (α) and beta (β) types.

Identification of Catecholamines

  • Catecholamines include dopamine, norepinephrine, and epinephrine; they are derived from tyrosine. A substance that does not fit this category, such as serotonin, is NOT classified as a catecholamine.

Sympathomimetic Amines

  • Sympathomimetic amines containing the 3,4-dihydroxybenzene group are classified as catecholamines. This structural feature is crucial for their activity as neurotransmitters.

Receptor Potency Comparison

  • Beta-adrenergic receptors, particularly β1 and β2 receptors, have higher potency for isoproterenol compared to epinephrine and norepinephrine, making isoproterenol a more effective agonist for these receptors.

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