Deck 16: Pharmacodynamics
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Deck 16: Pharmacodynamics
1
Pharmacological effect is achieved by:
A) the portion of free or unbound drug.
B) the portion of protein-bound drug.
C) ionisation.
D) penetrating the blood-brain barrier.
A) the portion of free or unbound drug.
B) the portion of protein-bound drug.
C) ionisation.
D) penetrating the blood-brain barrier.
the portion of free or unbound drug.
2
In disrupting the synthesis of folic acid in bacteria,sulfonamides act:
A) as competitive inhibitors.
B) as non-competitive inhibitors.
C) by physical action.
D) by none of the above.
A) as competitive inhibitors.
B) as non-competitive inhibitors.
C) by physical action.
D) by none of the above.
as competitive inhibitors.
3
In general,a medicine that acts by chemical or physical means can be identified by its dose,which is considerably higher than that required by medicines that act by interacting with a receptor or enzyme system.
True
4
Some terms that describe interactions between drugs and receptors include: (Select all that apply)
A) antagonism.
B) agonism.
C) first mechanism
D) first messenger
A) antagonism.
B) agonism.
C) first mechanism
D) first messenger
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5
Competitive inhibition slows down the rate of normal chemical reactions because:
A) the normal substrate is malfunctioning.
B) the target enzyme binds temporarily with a look-alike substrate rather than its actual substrate.
C) it takes a long time for the enzyme to develop memory or recognition of the competing substances.
D) it causes enzyme confusion.
A) the normal substrate is malfunctioning.
B) the target enzyme binds temporarily with a look-alike substrate rather than its actual substrate.
C) it takes a long time for the enzyme to develop memory or recognition of the competing substances.
D) it causes enzyme confusion.
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6
When a drug acts through non-competitive inhibition of an enzyme,it:
A) can be overcome by giving more of the enzyme substrate.
B) is usually reversible.
C) binds to a distinct site away from the active site.
D) is lethal to the person receiving treatment.
A) can be overcome by giving more of the enzyme substrate.
B) is usually reversible.
C) binds to a distinct site away from the active site.
D) is lethal to the person receiving treatment.
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7
The extent of binding of a drug to a receptor is termed:
A) potency.
B) specificity.
C) affinity.
D) efficacy.
A) potency.
B) specificity.
C) affinity.
D) efficacy.
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8
Pharmacodynamics describes the physiological processes that act on a drug once it enters the body,or how the body handles the drug.
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9
Which one of the following statements about pharmacodynamics is true?
A) A partial agonist can be as effective as an antagonist.
B) Ion channels do not have receptors.
C) Second messenger systems always involve G-proteins.
D) The antiasthma agent theophylline acts via a tyrosine kinase-linked receptor.
A) A partial agonist can be as effective as an antagonist.
B) Ion channels do not have receptors.
C) Second messenger systems always involve G-proteins.
D) The antiasthma agent theophylline acts via a tyrosine kinase-linked receptor.
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10
A drug mechanism that works to neutralise stomach acid is considered to be:
A) an action targeting ion channels.
B) a chemical action.
C) an agonist action.
D) a physical action.
A) an action targeting ion channels.
B) a chemical action.
C) an agonist action.
D) a physical action.
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